Item | Value |
---|---|
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 | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0002 | 0/0 | 928 | 36 | 2 | 12 | 10 | 6 | 6 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0003 | 0/0 | 928 | 23 | 1 | 12 | 0 | 1 | 9 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | MEVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0004 | 0/1 | 928 | 15 | 4 | 4 | 1 | 1 | 4 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0005 | 0/0 | 928 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0006 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0007 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0008 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
a0009 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | MDVGF others(923): Show |
chr1 | 114577850 | 114675049 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2784 | 213 | 61 | 35 | 103 | 1 | 12 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0001c0006 | 0/0 | 2784 | 2 | 0 | 0 | 1 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0001c0011 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0001c0012 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0001c0013 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0001c0014 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0002c0002 | 0/0 | 2784 | 35 | 2 | 12 | 10 | 6 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0002c0016 | 0/0 | 2784 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0003c0003 | 0/0 | 2784 | 22 | 1 | 11 | 0 | 1 | 9 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0003c0008 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0004c0004 | 0/1 | 2784 | 15 | 4 | 4 | 1 | 1 | 4 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0005c0007 | 0/0 | 2784 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0006c0005 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0007c0010 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0008c0015 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
chr1 | 114577850 | 114675049 | ||
a0009c0009 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | ATGGA others(2779): Show |
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 | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0002 | 1/0 | 6177 | 62 | 0 | 12 | 46 | 0 | 3 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0005 | 0/0 | 6178 | 7 | 0 | 2 | 5 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6173): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0006 | 0/0 | 6183 | 3 | 1 | 0 | 0 | 0 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6178): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0008 | 0/0 | 6181 | 3 | 2 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0009 | 0/0 | 6187 | 4 | 4 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6182): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0010 | 0/0 | 6179 | 3 | 0 | 2 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0011 | 0/0 | 6190 | 4 | 4 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6185): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0012 | 0/0 | 6184 | 4 | 3 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6179): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0013 | 0/0 | 6182 | 3 | 0 | 2 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6177): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0014 | 0/0 | 6179 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0016 | 0/0 | 6179 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0017 | 0/0 | 6183 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6178): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0018 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6175): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0019 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6184): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0020 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6190): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0021 | 0/0 | 6187 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6182): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0023 | 0/0 | 6178 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6173): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0024 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6180): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0025 | 0/0 | 6194 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6189): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0026 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0027 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0028 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0029 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0031 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6173): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0032 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6175): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0033 | 0/0 | 6178 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6173): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0034 | 0/0 | 6182 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6177): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0036 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6175): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0037 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6180): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0040 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0042 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0043 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0045 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0046 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6179): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0047 | 0/0 | 6176 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6171): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0048 | 0/0 | 6181 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0049 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0050 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0051 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6179): Show |
chr1 | 114577850 | 114675049 |
a0001c0001t0052 | 0/0 | 6177 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0006t0004 | 0/0 | 6177 | 2 | 0 | 0 | 1 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0001c0011t0044 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0012t0010 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0001c0013t0009 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6182): Show |
chr1 | 114577850 | 114675049 |
a0001c0014t0006 | 0/0 | 6183 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6178): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0001 | 0/0 | 6179 | 26 | 0 | 10 | 8 | 3 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0008 | 0/0 | 6181 | 2 | 1 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0015 | 0/0 | 6179 | 2 | 1 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0018 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6175): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0030 | 0/0 | 6181 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6176): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0035 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6180): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0038 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6175): Show |
chr1 | 114577850 | 114675049 |
a0002c0002t0041 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0002c0016t0001 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0003c0003t0003 | 0/0 | 6176 | 17 | 1 | 8 | 0 | 1 | 7 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6171): Show |
chr1 | 114577850 | 114675049 |
a0003c0003t0007 | 0/0 | 6177 | 4 | 0 | 2 | 0 | 0 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0003c0003t0039 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6173): Show |
chr1 | 114577850 | 114675049 |
a0003c0008t0007 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0004c0004t0004 | 0/1 | 6177 | 15 | 4 | 4 | 1 | 1 | 4 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0005c0007t0006 | 0/0 | 6183 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6178): Show |
chr1 | 114577850 | 114675049 |
a0006c0005t0022 | 0/0 | 6182 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6177): Show |
chr1 | 114577850 | 114675049 |
a0007c0010t0007 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
a0008c0015t0001 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6174): Show |
chr1 | 114577850 | 114675049 |
a0009c0009t0002 | 0/0 | 6177 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | GGAGC others(6172): Show |
chr1 | 114577850 | 114675049 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 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 |
a0001c0001t0001g0078 | 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 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0111 | 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 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 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 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0085 | 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 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0170 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0181 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | 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 |
a0001c0001t0002g0194 | 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 |
a0001c0001t0002g0198 | 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 |
a0001c0001t0002g0206 | 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 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0040 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0016g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0017g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0017g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0018g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0019g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0020g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0020g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0023g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0024g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0024g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0027g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0028g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0029g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0031g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0032g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0033g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0034g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0036g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0037g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0040g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0042g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0043g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0045g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0046g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0047g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0048g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0049g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0050g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0051g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0052g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0006t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0006t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0011t0044g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0012t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0013t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0014t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0008g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0015g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0015g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0018g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0030g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0035g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0038g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0041g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0016t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0003c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0275 | 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 |
a0003c0003t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0039g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0008t0007g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0004c0004t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0005c0007t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0005c0007t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0006c0005t0022g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0006c0005t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0007c0010t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0008c0015t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0009c0009t0002g0208 | 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 | g0240 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0012 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00140 | hp1 | a0002 | c0002 | t0035 | g0242 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00140 | hp2 | a0002 | c0002 | t0041 | g0256 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0255 | EUR | FIN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00323 | hp2 | a0001 | c0014 | t0006 | g0032 | EUR | FIN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00558 | hp2 | a0002 | c0002 | t0030 | g0233 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00642 | hp1 | a0001 | c0001 | t0050 | g0193 | 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 | g0085 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00733 | hp1 | a0002 | c0002 | t0015 | g0239 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00733 | hp2 | a0003 | c0003 | t0003 | g0013 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00735 | hp2 | a0003 | c0003 | t0003 | g0282 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00738 | hp2 | a0003 | c0003 | t0039 | g0278 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0268 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00741 | hp2 | a0001 | c0011 | t0044 | g0224 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0226 | 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 | g0263 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01081 | hp2 | a0003 | c0003 | t0003 | g0283 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0004 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01099 | hp2 | a0003 | c0003 | t0003 | g0272 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01106 | hp1 | a0003 | c0008 | t0007 | g0277 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0267 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0031 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01168 | hp2 | a0005 | c0007 | t0006 | g0036 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01169 | hp1 | a0005 | c0007 | t0006 | g0035 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01175 | hp2 | a0001 | c0001 | t0013 | g0040 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01192 | hp1 | a0004 | c0004 | t0004 | g0068 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01192 | hp2 | a0002 | c0002 | t0038 | g0250 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01257 | hp1 | a0004 | c0004 | t0004 | g0063 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0162 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01261 | hp1 | a0004 | c0004 | t0004 | g0065 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01261 | hp2 | a0001 | c0001 | t0049 | g0180 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01346 | hp1 | a0001 | c0001 | t0048 | g0161 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01346 | hp2 | a0003 | c0003 | t0007 | g0271 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01433 | hp1 | a0004 | c0004 | t0004 | g0053 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01496 | hp1 | a0001 | c0001 | t0031 | g0137 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0041 | 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 | g0254 | EUR | IBS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01884 | hp2 | a0001 | c0001 | t0019 | g0018 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01891 | hp1 | a0004 | c0004 | t0004 | g0074 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0014 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01928 | hp2 | a0001 | c0001 | t0032 | g0142 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01952 | hp2 | a0003 | c0003 | t0007 | g0281 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0138 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01993 | hp1 | a0001 | c0001 | t0010 | g0106 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02004 | hp2 | a0003 | c0003 | t0003 | g0013 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02055 | hp2 | a0007 | c0010 | t0007 | g0060 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02083 | hp1 | a0008 | c0015 | t0001 | g0076 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02145 | hp1 | a0001 | c0001 | t0045 | g0084 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02145 | hp2 | a0001 | c0001 | t0042 | g0023 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02257 | hp1 | a0006 | c0005 | t0022 | g0070 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02257 | hp2 | a0004 | c0004 | t0004 | g0073 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02258 | hp1 | a0001 | c0001 | t0021 | g0025 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0051 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02280 | hp2 | a0001 | c0001 | t0043 | g0016 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02451 | hp1 | a0001 | c0001 | t0029 | g0057 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02451 | hp2 | a0001 | c0001 | t0024 | g0058 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02572 | hp2 | a0001 | c0001 | t0020 | g0015 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02602 | hp2 | a0003 | c0003 | t0003 | g0280 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0252 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0273 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02698 | hp2 | a0001 | c0006 | t0004 | g0061 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02818 | hp2 | a0003 | c0003 | t0003 | g0011 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02886 | hp2 | a0001 | c0001 | t0046 | g0056 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02896 | hp1 | a0001 | c0001 | t0014 | g0079 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02896 | hp2 | a0001 | c0001 | t0040 | g0059 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0050 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0081 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02922 | hp2 | a0004 | c0004 | t0004 | g0072 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02976 | hp1 | a0001 | c0001 | t0051 | g0075 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0012 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03041 | hp1 | a0001 | c0001 | t0021 | g0027 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03098 | hp2 | a0004 | c0004 | t0004 | g0054 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0261 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0251 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03239 | hp1 | a0003 | c0003 | t0003 | g0274 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03490 | hp1 | a0004 | c0004 | t0004 | g0089 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0284 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0285 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03540 | hp1 | a0001 | c0001 | t0036 | g0029 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03540 | hp2 | a0002 | c0002 | t0008 | g0262 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03654 | hp1 | a0004 | c0004 | t0004 | g0218 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03654 | hp2 | a0003 | c0003 | t0003 | g0275 | 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 | g0064 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0270 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03834 | hp1 | a0001 | c0001 | t0013 | g0034 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03834 | hp2 | a0003 | c0003 | t0007 | g0276 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03927 | hp1 | a0004 | c0004 | t0004 | g0067 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04115 | hp1 | a0001 | c0001 | t0027 | g0099 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0038 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04184 | hp2 | a0003 | c0003 | t0007 | g0279 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18612 | hp2 | a0001 | c0001 | t0017 | g0028 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0221 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18957 | hp2 | a0001 | c0001 | t0017 | g0026 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0135 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18960 | hp2 | a0009 | c0009 | t0002 | g0208 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0107 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18964 | hp2 | a0004 | c0004 | t0004 | g0069 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18966 | hp1 | a0001 | c0001 | t0052 | g0197 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18967 | hp1 | a0001 | c0001 | t0018 | g0122 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18969 | hp1 | a0001 | c0001 | t0047 | g0205 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18986 | hp1 | a0001 | c0006 | t0004 | g0062 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0091 | 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 | g0188 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19010 | hp2 | a0002 | c0002 | t0018 | g0249 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19011 | hp1 | a0001 | c0012 | t0010 | g0094 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19055 | hp1 | a0001 | c0001 | t0033 | g0030 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19055 | hp2 | a0001 | c0001 | t0034 | g0140 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0203 | 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 | g0174 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19240 | hp1 | a0001 | c0001 | t0023 | g0052 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ASW | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20129 | hp2 | a0001 | c0001 | t0019 | g0017 | AFR | ASW | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20752 | hp1 | a0002 | c0002 | t0008 | g0234 | EUR | TSI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20752 | hp2 | a0004 | c0004 | t0004 | g0066 | EUR | TSI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20905 | hp1 | a0002 | c0016 | t0001 | g0259 | SAS | GIH | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0037 | SAS | GIH | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01123 | hp2 | a0003 | c0003 | t0003 | g0269 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02109 | hp1 | a0001 | c0001 | t0024 | g0220 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02109 | hp2 | a0001 | c0013 | t0009 | g0019 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0144 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02559 | hp1 | a0002 | c0002 | t0015 | g0237 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG06807 | hp1 | a0001 | c0001 | t0028 | g0266 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0048 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18955 | hp2 | a0001 | c0001 | t0037 | g0039 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA21309 | hp1 | a0006 | c0005 | t0022 | g0071 | AFR | LWK | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
homoSapiens | chm13v2 | a0004 | c0004 | t0004 | g0055 | REF | REF | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0183 | REF | REF | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114600249 | 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 | 14 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(11): 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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114587732 | C | T | 2 | a0001c0006 a0004c0004 |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114582859 | 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 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0017 others(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 | a0001c0001t0009 a0001c0013t0009 |
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 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0013 others(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 | a0001c0001t0029 a0001c0001t0037 a0001c0001t0040 others(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 | a0001c0001t0012 a0001c0001t0024 a0001c0001t0046 others(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 | a0001c0001t0020 a0001c0001t0025 |
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 | a0002c0002t0015 a0002c0002t0038 |
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 | a0001c0001t0017 a0001c0001t0034 a0001c0001t0037 others(2): Show |
20 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(17): 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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(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 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0031 others(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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0001t0010 a0001c0001t0031 a0001c0001t0032 others(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 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0021 others(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 | a0001c0001t0012 a0001c0001t0023 a0001c0001t0024 others(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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(54): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114585828 | C | T | 1 | a0001c0001t0051g0075 | 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 | a0001c0001t0002g0211 | 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 | a0004c0004t0004g0073 a0004c0004t0004g0074 |
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 | a0001c0001t0019g0018 | 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 | 35 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(32): 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 | a0001c0001t0014g0079 a0001c0001t0014g0081 |
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 | a0001c0001t0002g0173 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0129 a0001c0001t0002g0209 a0001c0001t0006g0033 others(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 | a0001c0001t0024g0220 | 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 | a0008c0015t0001g0076 | 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 | a0002c0002t0001g0235 a0002c0002t0001g0238 a0002c0002t0008g0234 others(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 | a0001c0001t0002g0176 | 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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 |
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 | a0002c0002t0030g0233 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0040g0059 | 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 | a0003c0003t0003g0270 | 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 | a0001c0001t0002g0185 | 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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0001g0125 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 |
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 | a0001c0011t0044g0224 | 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 | a0003c0003t0003g0272 a0003c0003t0003g0273 a0003c0003t0003g0275 others(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 | a0001c0011t0044g0224 | 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 | a0001c0001t0043g0016 | 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0001g0112 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0002c0002t0001g0235 a0002c0002t0001g0238 a0002c0002t0008g0234 others(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 | a0001c0001t0024g0058 a0006c0005t0022g0070 a0006c0005t0022g0071 |
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 | a0001c0001t0002g0181 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0001g0119 | 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 | a0002c0002t0001g0232 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2432-2754T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590706 | |||||||
chr1:114590773 | C | T | 36 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(33): 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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(155): 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 | 31 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0127 others(28): 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 | 17 | a0001c0001t0002g0010 a0001c0001t0002g0191 a0001c0001t0002g0215 others(14): 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 | a0004c0004t0004g0067 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0016g0251 a0001c0001t0016g0252 |
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 | a0001c0001t0002g0200 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | 21 | a0001c0001t0011g0047 a0003c0003t0003g0011 a0003c0003t0003g0012 others(18): 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 | a0001c0001t0002g0173 a0001c0001t0002g0194 |
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 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0154 | 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 | a0002c0002t0001g0230 | 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0005g0166 | 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 | a0002c0002t0015g0237 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0004c0004t0004g0069 | 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 | 11 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(8): 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 | a0001c0001t0001g0222 a0002c0002t0001g0230 a0002c0002t0001g0236 others(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 | a0001c0001t0002g0199 | 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 | a0001c0001t0045g0084 | 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 | a0001c0001t0001g0077 a0001c0001t0018g0122 |
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 | a0002c0002t0001g0045 a0002c0002t0001g0230 a0002c0002t0001g0231 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(77): 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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0002c0002t0001g0240 a0002c0002t0001g0246 a0002c0002t0001g0255 |
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 | 14 | a0004c0004t0004g0053 a0004c0004t0004g0054 a0004c0004t0004g0063 others(11): Show |
14 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(11): 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0045g0084 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0052g0197 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0002c0002t0001g0258 a0002c0016t0001g0259 |
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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0002c0002t0015g0239 a0002c0002t0030g0233 |
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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 |
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 | a0001c0013t0009g0019 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0005g0171 | 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 | a0001c0006t0004g0061 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0011t0044g0224 | 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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): 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 | a0001c0001t0023g0051 | 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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2106-318C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599769 | |||||||
chr1:114599822 | T | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(144): 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 | a0003c0003t0003g0273 | 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 | a0001c0001t0014g0079 a0001c0001t0014g0081 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0021g0027 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0002g0170 a0001c0001t0002g0198 a0001c0001t0002g0202 |
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 | a0002c0002t0001g0238 a0002c0002t0015g0237 a0002c0002t0015g0239 others(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 | a0004c0004t0004g0069 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0005g0162 | 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 | 282 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(279): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): 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 | a0001c0001t0002g0202 | 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 | a0002c0002t0001g0253 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0002c0002t0008g0234 | 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 | a0001c0001t0002g0202 | 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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(143): 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1668-949delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603142 | |||||||
chr1:114603269 | T | C | 1 | a0001c0001t0001g0121 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0143 |
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 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0191 others(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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(128): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0021g0027 | 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 | a0001c0001t0023g0051 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(128): 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0020g0014 a0001c0001t0020g0015 a0001c0001t0021g0027 |
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 | a0001c0011t0044g0224 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0001t0002g0042 | 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 | a0001c0001t0010g0107 | 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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): 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 | a0002c0002t0008g0234 | 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 | a0004c0004t0004g0054 a0004c0004t0004g0072 |
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 | a0001c0001t0001g0121 | 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 | a0001c0011t0044g0224 | 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 | 4 | a0001c0001t0002g0010 a0001c0001t0002g0215 a0001c0001t0002g0216 others(1): 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 | a0001c0001t0021g0027 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(160): 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 | a0001c0001t0001g0222 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0004c0004t0004g0067 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0002c0002t0001g0240 a0002c0002t0001g0246 a0002c0002t0001g0255 |
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 | a0002c0002t0001g0254 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0002g0204 | 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 | 35 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(32): 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369+603C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610470 | |||||||
chr1:114610471 | C | T | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369+602G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610471 | |||||||
chr1:114610472 | A | G | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0002g0007 a0001c0001t0002g0172 a0001c0001t0002g0175 others(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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0136 a0001c0001t0002g0186 others(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 | a0002c0002t0001g0240 | 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 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0160 others(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 | a0002c0002t0001g0263 a0002c0002t0001g0265 |
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 | a0002c0002t0015g0237 | 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(160): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 19 | a0001c0001t0002g0211 a0001c0001t0005g0162 a0001c0001t0005g0171 others(16): Show |
19 | HG00099.hp2 HG01099.hp2 HG01192.hp1 others(16): 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 | 29 | a0001c0001t0009g0020 a0001c0001t0012g0004 a0001c0001t0023g0051 others(26): 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 | a0001c0001t0013g0034 a0001c0001t0020g0014 a0001c0001t0036g0029 others(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 | a0001c0001t0006g0033 a0001c0001t0006g0038 a0001c0001t0009g0021 others(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 | a0001c0001t0021g0027 a0001c0001t0037g0039 a0003c0003t0003g0270 |
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 | a0001c0001t0009g0022 a0001c0001t0013g0040 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0041 a0001c0001t0002g0043 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0159 a0002c0002t0001g0241 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(116): 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 | a0001c0001t0001g0098 a0002c0002t0001g0045 a0002c0002t0001g0230 |
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 | a0001c0001t0047g0205 | 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 | a0001c0006t0004g0061 a0001c0006t0004g0062 |
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 | a0001c0001t0001g0105 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(113): 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 | 16 | a0001c0001t0002g0212 a0001c0006t0004g0061 a0001c0006t0004g0062 others(13): Show |
16 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1325-1404dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114612520 | |||||||
chr1:114612548 | C | G | 1 | a0001c0001t0001g0124 | 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0013g0034 | 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 | a0001c0001t0040g0059 | 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 | a0001c0001t0002g0213 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0021g0027 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(89): 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0001g0093 a0007c0010t0007g0060 |
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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1325-3463dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614579 | |||||||
chr1:114614907 | G | A | 1 | a0001c0001t0001g0118 | 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 | a0001c0001t0011g0047 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0093 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0003c0003t0007g0279 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0013t0009g0019 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0004c0004t0004g0053 a0004c0004t0004g0054 a0004c0004t0004g0072 |
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 | a0001c0001t0008g0148 | 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 | a0001c0001t0024g0058 a0001c0006t0004g0062 a0006c0005t0022g0070 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 23 | a0001c0001t0001g0121 a0001c0001t0001g0226 a0001c0001t0001g0228 others(20): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0023g0052 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(128): 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | 11 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(8): 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 | a0001c0001t0045g0084 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0002g0215 | 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 | a0001c0001t0002g0187 | 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 | a0004c0004t0004g0089 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0002g0194 | 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 | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(65): 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 14 | a0004c0004t0004g0053 a0004c0004t0004g0054 a0004c0004t0004g0063 others(11): Show |
14 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(11): 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0013g0031 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0160 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0036g0029 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0009g0022 a0001c0001t0009g0024 |
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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0002c0002t0001g0240 a0002c0002t0001g0246 a0002c0002t0001g0255 |
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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0002g0170 a0001c0001t0002g0198 a0001c0001t0002g0202 |
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 | 7 | a0003c0003t0003g0011 a0003c0003t0003g0013 a0003c0003t0003g0267 others(4): 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 | a0001c0001t0001g0150 a0001c0001t0001g0157 |
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 | 6 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(3): 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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(142): 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(196): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.806+554delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624624 | |||||||
chr1:114624653 | G | A | 2 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0002c0002t0001g0231 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0029g0057 | 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 | a0001c0001t0002g0178 a0001c0001t0002g0188 |
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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0001g0088 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0001g0114 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(135): 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 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0003c0003t0039g0278 | 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 | a0001c0001t0013g0040 | 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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(199): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): 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 | a0001c0001t0002g0006 a0001c0001t0002g0189 a0001c0001t0002g0190 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(193): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0012g0221 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0020g0014 a0001c0001t0020g0015 a0001c0001t0021g0027 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0223 a0001c0001t0009g0020 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0013t0009g0019 | 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 | a0001c0013t0009g0019 | 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 | a0001c0001t0001g0134 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0007c0010t0007g0060 | 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 | a0004c0004t0004g0073 a0004c0004t0004g0074 |
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 | a0004c0004t0004g0066 | 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 | a0001c0001t0027g0099 | 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 | a0001c0001t0002g0210 | 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 | a0002c0002t0001g0235 a0002c0002t0041g0256 |
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 | a0001c0006t0004g0061 a0001c0006t0004g0062 |
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 | a0001c0001t0029g0057 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0024g0220 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0001g0086 | 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 | a0001c0011t0044g0224 | 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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(143): 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 | a0001c0013t0009g0019 | 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 | 11 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(8): 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 | a0001c0001t0002g0192 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0002c0002t0001g0236 a0002c0002t0001g0247 |
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 | 3 | a0001c0001t0002g0010 a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0011t0044g0224 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(130): 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 | a0001c0001t0040g0059 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 a0001c0001t0021g0027 |
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 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0225 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 6 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(3): 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 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0128 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0021g0027 | 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 | a0001c0001t0016g0251 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0225 a0001c0001t0008g0148 others(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 | a0001c0001t0016g0251 | 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 | a0001c0001t0016g0251 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0002g0175 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0226 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0219 | 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 | a0001c0001t0013g0031 | 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 | a0001c0001t0037g0039 | 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 | a0002c0002t0001g0248 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0132 a0002c0002t0001g0230 others(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 | a0002c0002t0001g0045 a0002c0002t0001g0235 a0002c0002t0001g0238 others(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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0002c0002t0035g0242 | 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 | a0002c0002t0015g0237 a0002c0002t0015g0239 a0002c0002t0038g0250 |
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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0093 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0036g0029 | 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 | a0001c0001t0048g0161 | 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 | a0001c0001t0024g0058 | 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 | a0001c0001t0002g0204 a0001c0001t0002g0206 a0001c0001t0002g0207 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0118 |
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 | a0002c0002t0001g0240 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-205+8609A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636839 | |||||||
chr1:114636880 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0011t0044g0224 | 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(208): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-205+8342dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637105 | |||||||
chr1:114637309 | T | C | 1 | a0001c0001t0002g0174 | 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 | 29 | a0001c0001t0002g0175 a0001c0001t0009g0020 a0001c0001t0009g0021 others(26): Show |
29 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.-205+8078delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637369 | |||||||
chr1:114637369 | CAAAAAA | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(144): 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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(144): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0036g0029 | 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 | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0001c0001t0002g0177 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-205+6820G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638628 | |||||||
chr1:114638762 | CA | C | 90 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(87): Show |
95 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(92): 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-205+6462A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638986 | |||||||
chr1:114639222 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0051g0075 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(144): 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 | a0002c0002t0015g0237 | 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 | a0001c0001t0001g0229 a0001c0001t0010g0106 a0001c0001t0010g0107 others(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 | a0001c0001t0014g0079 a0001c0001t0014g0081 |
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 | a0003c0003t0003g0272 a0003c0003t0007g0281 |
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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0096 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0149 a0001c0001t0001g0225 a0001c0001t0008g0148 |
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 | a0001c0001t0014g0079 a0001c0001t0014g0081 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 218 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(215): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-205+4237A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641211 | |||||||
chr1:114641260 | CA | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-205+4187delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641260 | |||||||
chr1:114641596 | C | G | 13 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0004c0004t0004g0089 | 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 | a0007c0010t0007g0060 | 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 | 16 | a0001c0001t0002g0006 a0001c0001t0002g0173 a0001c0006t0004g0062 others(13): Show |
17 | HG01192.hp1 HG01261.hp1 HG01433.hp1 others(14): 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 | a0009c0009t0002g0208 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0001c0001t0023g0051 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-205+1597dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114643850 | |||||||
chr1:114644344 | A | G | 14 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0043g0016 | 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 | a0001c0001t0029g0057 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0024g0220 | 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 | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0001c0001t0029g0057 | 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 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
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 | a0001c0001t0001g0136 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(147): 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 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
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 | a0001c0001t0001g0091 | 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 | a0002c0002t0001g0045 a0002c0002t0001g0230 a0002c0002t0001g0231 others(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 | a0001c0011t0044g0224 | 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 | 7 | a0003c0003t0003g0011 a0003c0003t0003g0013 a0003c0003t0003g0267 others(4): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0002c0002t0001g0240 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0117 a0001c0001t0001g0227 |
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 | a0003c0003t0003g0270 | 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 | 7 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(4): 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 | a0002c0002t0001g0238 a0002c0002t0015g0237 a0002c0002t0015g0239 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0225 others(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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(130): 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 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0047g0205 others(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 | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(273): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0002c0002t0001g0235 a0002c0002t0041g0256 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0118 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(147): 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 | a0001c0001t0019g0017 a0001c0001t0019g0018 |
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 | a0001c0001t0047g0205 | 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 | a0001c0006t0004g0062 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0198 | 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 | a0001c0001t0008g0144 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0011g0049 | 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 | a0001c0001t0024g0058 | 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 | a0003c0003t0007g0279 | 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 | a0001c0011t0044g0224 | 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 | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0001g0136 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0002g0199 | 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 | a0001c0001t0029g0057 | 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 | a0001c0001t0002g0211 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | 19 | a0001c0001t0001g0078 a0001c0001t0002g0173 a0001c0001t0017g0026 others(16): Show |
19 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-317+4181delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650323 | |||||||
chr1:114650354 | T | C | 1 | a0007c0010t0007g0060 | 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 | a0001c0001t0024g0220 | 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 | 52 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(49): Show |
56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.-317+4075G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650430 | |||||||
chr1:114650567 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0103 a0001c0011t0044g0224 |
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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(144): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | 12 | a0001c0001t0002g0172 a0001c0001t0002g0203 a0001c0001t0002g0204 others(9): 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-317+3746A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650759 | |||||||
chr1:114650928 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0002c0002t0001g0235 a0002c0002t0008g0234 a0002c0002t0041g0256 |
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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(127): 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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(199): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): 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 | a0001c0001t0001g0101 | 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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(125): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): 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 | 49 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0100 others(46): 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | a0001c0001t0013g0031 a0001c0014t0006g0032 a0003c0003t0003g0269 |
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 | a0001c0001t0021g0027 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0009g0024 a0001c0001t0019g0017 a0001c0001t0019g0018 others(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 | a0001c0001t0029g0057 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0165 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0093 | 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 | a0002c0002t0001g0253 | 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 | 36 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(33): 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 | a0001c0001t0013g0040 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0100 a0001c0001t0002g0009 a0001c0001t0002g0203 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(120): 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 | 49 | a0001c0001t0001g0087 a0001c0001t0001g0128 a0001c0001t0001g0129 others(46): Show |
50 | HG00323.hp1 HG00323.hp2 HG00741.hp2 others(47): 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 | 33 | a0001c0001t0012g0004 a0001c0001t0012g0221 a0001c0001t0023g0051 others(30): 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 | a0001c0001t0012g0050 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 |
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 | a0001c0001t0001g0082 | 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 | a0004c0004t0004g0053 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0001g0136 | 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0002g0168 a0001c0001t0002g0211 a0001c0001t0005g0169 others(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 | 8 | a0004c0004t0004g0063 a0004c0004t0004g0064 a0004c0004t0004g0065 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-317+1111G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653394 | |||||||
chr1:114653400 | C | T | 14 | a0004c0004t0004g0053 a0004c0004t0004g0054 a0004c0004t0004g0063 others(11): Show |
14 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(11): 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 others(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 | a0001c0001t0011g0047 | 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 | a0001c0001t0021g0027 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0020g0014 | 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 | a0001c0001t0002g0210 | 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 | 23 | a0001c0001t0001g0086 a0001c0001t0001g0132 a0001c0001t0011g0003 others(20): Show |
24 | HG00735.hp2 HG01192.hp1 HG01257.hp1 others(21): 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 | a0001c0001t0001g0098 a0001c0001t0001g0136 a0001c0001t0001g0147 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0019g0017 a0001c0001t0019g0018 |
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 | a0002c0002t0041g0256 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0133 | 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 | a0002c0002t0001g0232 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 |
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 | a0001c0001t0009g0020 a0001c0001t0009g0021 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0034g0140 |
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 | a0001c0001t0001g0087 a0001c0001t0001g0120 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0155 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0001 | 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 | a0001c0001t0019g0017 a0001c0001t0019g0018 a0001c0001t0021g0027 others(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 | 38 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(35): Show |
39 | HG00323.hp2 HG00735.hp1 HG01167.hp1 others(36): 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0144 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0223 a0001c0001t0012g0004 a0001c0001t0012g0221 others(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 | a0001c0001t0023g0052 | 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 | a0001c0001t0012g0004 | 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 | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(79): 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 | a0001c0001t0001g0225 a0001c0001t0008g0148 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0002g0211 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(135): 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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0006g0033 others(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 | a0007c0010t0007g0060 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0082 | 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0043g0016 | 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 | a0001c0013t0009g0019 | 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 | a0001c0001t0013g0031 a0001c0014t0006g0032 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0002g0168 a0001c0001t0005g0169 |
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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0008g0135 | 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 | a0001c0011t0044g0224 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-573-3426T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658187 | |||||||
chr1:114658436 | G | A | 12 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(9): 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0150 | 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 | a0007c0010t0007g0060 | 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 | a0001c0012t0010g0094 | 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 |
19 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(16): 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 | a0003c0003t0003g0273 | 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 | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0002c0002t0001g0257 | 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 | a0001c0011t0044g0224 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
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 | 14 | a0004c0004t0004g0053 a0004c0004t0004g0054 a0004c0004t0004g0063 others(11): Show |
14 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-573-4668C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659429 | |||||||
chr1:114659594 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(130): 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 4 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(1): 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 | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(211): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): 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 | a0007c0010t0007g0060 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0033g0030 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0141 |
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 | a0001c0001t0005g0167 | 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 | a0001c0001t0002g0213 | 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 | a0003c0003t0003g0013 | 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 | a0003c0003t0003g0013 | 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 | 53 | a0001c0001t0001g0139 a0001c0001t0009g0020 a0001c0001t0009g0021 others(50): 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(120): 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 | a0004c0004t0004g0069 | 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 | a0001c0001t0036g0029 | 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 | a0001c0001t0032g0142 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0036g0029 | 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 | a0006c0005t0022g0071 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0143 |
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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-573-7085G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661846 | |||||||
chr1:114662011 | GATTAA | G | 34 | a0001c0001t0012g0004 a0001c0001t0012g0050 a0001c0001t0012g0221 others(31): 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0005g0166 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0144 others(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 | 23 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0149 others(20): 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0024g0220 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 1 | a0003c0003t0003g0011 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | a0001c0001t0026g0261 | 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 | a0001c0001t0013g0040 | 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 | a0001c0001t0002g0165 | 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 | 14 | a0001c0001t0001g0219 a0001c0001t0002g0164 a0001c0001t0005g0162 others(11): Show |
15 | HG01257.hp1 HG01257.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.-574+6031dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663951 | |||||||
chr1:114663951 | CT | C | 7 | a0001c0001t0002g0010 a0001c0001t0002g0214 a0001c0001t0002g0215 others(4): 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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-574+5907G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664076 | |||||||
chr1:114664077 | C | A | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0028g0266 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(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 | 16 | a0001c0006t0004g0061 a0001c0006t0004g0062 a0004c0004t0004g0053 others(13): Show |
16 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-574+5062G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664921 | |||||||
chr1:114664938 | CA | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-574+5044delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664938 | |||||||
chr1:114665115 | A | G | 1 | a0002c0002t0001g0231 | 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 | a0002c0002t0008g0262 | 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 | a0001c0001t0045g0084 | 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(208): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-574+4711delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665271 | |||||||
chr1:114665542 | C | T | 1 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | a0001c0001t0040g0059 | 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 | a0001c0001t0020g0014 a0001c0001t0020g0015 |
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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0160 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-574+3554A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666429 | |||||||
chr1:114666521 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0005g0217 | 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 | a0001c0001t0017g0028 | 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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0004c0004t0004g0053 | 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 | a0007c0010t0007g0060 | 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 | a0001c0006t0004g0061 a0001c0006t0004g0062 |
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 | a0001c0006t0004g0061 a0001c0006t0004g0062 |
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 | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0077 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0003c0003t0007g0281 | 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 | a0001c0001t0021g0027 | 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 | a0001c0001t0021g0027 | 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 | a0001c0001t0012g0050 | 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0086 others(118): 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(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 | 27 | a0001c0001t0019g0017 a0001c0001t0019g0018 a0001c0013t0009g0019 others(24): 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 |
16 | a0001c0001t0012g0004 a0001c0001t0020g0014 a0001c0001t0020g0015 others(13): Show |
17 | HG01099.hp1 HG01099.hp2 HG01346.hp2 others(14): 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 | a0001c0001t0012g0050 a0001c0001t0023g0051 a0001c0001t0023g0052 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(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 | a0003c0003t0003g0283 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0047 a0001c0001t0011g0049 others(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 | a0001c0001t0016g0251 a0001c0001t0016g0252 a0001c0001t0026g0261 others(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 | a0003c0003t0003g0267 a0003c0003t0003g0268 a0003c0003t0003g0269 |
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 | a0001c0001t0002g0046 | 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 | a0002c0002t0001g0045 | 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 | a0001c0001t0028g0266 | 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 | 20 | a0003c0003t0003g0011 a0003c0003t0003g0012 a0003c0003t0003g0013 others(17): 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 | a0001c0001t0002g0044 | 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 | a0002c0002t0001g0284 a0002c0002t0001g0285 |
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 | 4 | a0001c0001t0002g0002 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): 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 | a0001c0001t0006g0033 a0001c0001t0006g0037 a0001c0001t0006g0038 others(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 |