Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 121441 |
| ensemblid | ENSG00000139350.12 |
| hgncid | 7723 |
| symbol | NEDD1 |
| name | NEDD1 gamma-tubulin ring complex targeting factor |
| refseq_nuc | NM_152905.4 |
| refseq_prot | NP_690869.1 |
| ensembl_nuc | ENST00000266742.9 |
| ensembl_prot | ENSP00000266742.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 96907257 |
| end | 96953780 |
| strand | + |
| ver | v1.2 |
| region | chr12:96907257-96953780 |
| region5000 | chr12:96902257-96958780 |
| regionname0 | NEDD1_chr12_96907257_96953780 |
| regionname5000 | NEDD1_chr12_96902257_96958780 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 660 | 394 | 88 | 72 | 183 | 14 | 35 | 143 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| a0002 | 0/0 | 660 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| a0003 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| a0004 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| a0005 | 0/0 | 660 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| a0006 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | MQENL others(655): Show |
chr12 | 96902257 | 96958780 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1980 | 387 | 81 | 72 | 183 | 14 | 35 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0001c0002 | 0/0 | 1980 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0001c0006 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0002c0003 | 0/0 | 1980 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0003c0008 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0004c0005 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0005c0004 | 0/0 | 1980 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 | ||
| a0006c0007 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | ATGCA others(1975): Show |
chr12 | 96902257 | 96958780 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4015 | 132 | 28 | 22 | 66 | 0 | 15 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0002 | 0/0 | 4015 | 99 | 8 | 26 | 46 | 10 | 9 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0003 | 1/0 | 4015 | 54 | 1 | 11 | 37 | 0 | 4 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0004 | 0/0 | 4016 | 27 | 1 | 5 | 21 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0005 | 0/0 | 4015 | 22 | 5 | 5 | 5 | 4 | 3 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0006 | 0/0 | 4015 | 13 | 11 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0007 | 0/0 | 4016 | 7 | 7 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0008 | 0/0 | 4015 | 5 | 1 | 0 | 0 | 0 | 4 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0009 | 0/0 | 4015 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0011 | 0/0 | 4016 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0012 | 0/0 | 4015 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0013 | 0/0 | 4015 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0014 | 0/0 | 4342 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4337): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0015 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0016 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0017 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0018 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0019 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0020 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0021 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0022 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0023 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0024 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0001t0025 | 0/0 | 4015 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0002t0010 | 0/0 | 4015 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0001c0006t0006 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0002c0003t0003 | 0/0 | 4015 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0003c0008t0007 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4011): Show |
chr12 | 96902257 | 96958780 |
| a0004c0005t0009 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0005c0004t0008 | 0/0 | 4015 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| a0006c0007t0001 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | AGCGC others(4010): Show |
chr12 | 96902257 | 96958780 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0013g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0017g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0019g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0020g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0021g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0022g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0023g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0024g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0025g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0006t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0002c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0002c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0003c0008t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0004c0005t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0005c0004t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0006c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0037 | EUR | GBR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0037 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0274 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01255 | hp1 | a0001 | c0001 | t0025 | g0143 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01884 | hp1 | a0001 | c0006 | t0006 | g0287 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0162 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0151 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CDX | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0292 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0288 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02451 | hp2 | a0001 | c0002 | t0010 | g0279 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0167 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02622 | hp2 | a0001 | c0001 | t0023 | g0322 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0082 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0236 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02895 | hp2 | a0001 | c0002 | t0010 | g0077 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0312 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0076 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0314 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02922 | hp2 | a0003 | c0008 | t0007 | g0315 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0051 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02976 | hp1 | a0004 | c0005 | t0009 | g0016 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0313 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0073 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03239 | hp2 | a0005 | c0004 | t0008 | g0208 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03453 | hp1 | a0001 | c0002 | t0010 | g0280 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0205 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0286 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03579 | hp1 | a0001 | c0002 | t0010 | g0075 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0081 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0222 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0311 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0309 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0224 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0261 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0050 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0067 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0180 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18963 | hp2 | a0001 | c0001 | t0017 | g0266 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18971 | hp1 | a0002 | c0003 | t0003 | g0181 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18974 | hp1 | a0001 | c0001 | t0012 | g0096 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19064 | hp1 | a0001 | c0001 | t0018 | g0138 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19067 | hp2 | a0001 | c0001 | t0012 | g0097 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19081 | hp2 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19086 | hp2 | a0006 | c0007 | t0001 | g0246 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19089 | hp1 | a0001 | c0001 | t0024 | g0080 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ASW | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20129 | hp2 | a0001 | c0001 | t0022 | g0195 | AFR | ASW | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0038 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0039 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0115 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | GIH | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0301 | SAS | GIH | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02109 | hp1 | a0001 | c0002 | t0010 | g0074 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0230 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18955 | hp2 | a0001 | c0001 | t0012 | g0099 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0310 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0212 | REF | REF | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0304 | REF | REF | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96920078 | G | A | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.442G>A | p.Val148Ile | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/16 | 747/4015 | 442/1983 | 148/660 | chr12 | 96920078 | |||
| chr12:96943694 | C | A | 1 | a0006 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1429C>A | p.Arg477Ser | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/16 | 1734/4015 | 1429/1983 | 477/660 | chr12 | 96943694 | |||
| chr12:96944701 | C | A | 1 | a0002 | 2 | NA18959.hp2 NA18971.hp1 |
missense_variant | MODERATE | c.1560C>A | p.Asn520Lys | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/16 | 1865/4015 | 1560/1983 | 520/660 | chr12 | 96944701 | |||
| chr12:96945695 | C | G | 1 | a0003 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.1657C>G | p.Pro553Ala | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/16 | 1962/4015 | 1657/1983 | 553/660 | chr12 | 96945695 | |||
| chr12:96945828 | A | G | 1 | a0005 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1790A>G | p.Gln597Arg | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/16 | 2095/4015 | 1790/1983 | 597/660 | chr12 | 96945828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96912817 | G | A | 1 | a0005c0004 | 1 | HG03239.hp2 | splice_region_variant&synonymous_variant | LOW | c.231G>A | p.Gly77Gly | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/16 | 536/4015 | 231/1983 | 77/660 | chr12 | 96912817 | |||
| chr12:96940443 | T | C | 1 | a0001c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1152T>C | p.Ser384Ser | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/16 | 1457/4015 | 1152/1983 | 384/660 | chr12 | 96940443 | |||
| chr12:96943708 | T | C | 1 | a0001c0002 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
synonymous_variant | LOW | c.1443T>C | p.Ala481Ala | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/16 | 1748/4015 | 1443/1983 | 481/660 | chr12 | 96943708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96907296 | G | T | 1 | a0001c0001t0011 | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-266G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/16 | 2464 | chr12 | 96907296 | ||||||
| chr12:96907648 | C | T | 1 | a0001c0001t0025 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/16 | 2112 | chr12 | 96907648 | ||||||
| chr12:96952083 | A | T | 1 | a0001c0001t0024 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 30 | chr12 | 96952083 | ||||||
| chr12:96952177 | A | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*124A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 124 | chr12 | 96952177 | ||||||
| chr12:96952347 | A | G | 1 | a0001c0002t0010 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*294A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 294 | chr12 | 96952347 | ||||||
| chr12:96952352 | A | T | 1 | a0001c0001t0023 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 299 | chr12 | 96952352 | ||||||
| chr12:96952429 | G | A | 1 | a0001c0001t0015 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*376G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 376 | chr12 | 96952429 | ||||||
| chr12:96952445 | A | C | 1 | a0001c0001t0022 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*392A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 392 | chr12 | 96952445 | ||||||
| chr12:96952501 | T | C | 2 | a0001c0001t0008 a0005c0004t0008 |
6 | HG03239.hp2 HG03490.hp1 HG03654.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 448 | chr12 | 96952501 | ||||||
| chr12:96952538 | C | T | 1 | a0001c0001t0021 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 485 | chr12 | 96952538 | ||||||
| chr12:96952642 | T | C | 1 | a0001c0001t0016 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 589 | chr12 | 96952642 | ||||||
| chr12:96952727 | A | G | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0019 others(2): Show |
35 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 674 | chr12 | 96952727 | ||||||
| chr12:96952822 | A | G | 2 | a0001c0001t0009 a0004c0005t0009 |
6 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*769A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 769 | chr12 | 96952822 | ||||||
| chr12:96952882 | C | CT | 3 | a0001c0001t0007 a0001c0001t0014 a0003c0008t0007 |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*834dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 835 | INFO_REALIGN_3_PRIME | chr12 | 96952882 | |||||
| chr12:96953013 | A | G | 1 | a0001c0001t0018 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 960 | chr12 | 96953013 | ||||||
| chr12:96953146 | G | A | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(16): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*1093G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1093 | chr12 | 96953146 | ||||||
| chr12:96953209 | T | TA | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0016 others(2): Show |
35 | HG01123.hp2 HG01358.hp1 HG01891.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1169dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1170 | INFO_REALIGN_3_PRIME | chr12 | 96953209 | |||||
| chr12:96953216 | A | C | 2 | a0001c0001t0006 a0001c0006t0006 |
14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1163A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1163 | chr12 | 96953216 | ||||||
| chr12:96953343 | T | C | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1290 | chr12 | 96953343 | ||||||
| chr12:96953407 | A | G | 1 | a0001c0002t0010 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1354A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1354 | chr12 | 96953407 | ||||||
| chr12:96953524 | C | A | 1 | a0001c0001t0012 | 3 | NA18955.hp2 NA18974.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1471C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1471 | chr12 | 96953524 | ||||||
| chr12:96953536 | T | TCCTGTTG others(319): Show |
1 | a0001c0001t0014 | 2 | HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1497_*1498insTTTT others(322): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1498 | INFO_REALIGN_3_PRIME | chr12 | 96953536 | |||||
| chr12:96953583 | G | T | 1 | a0001c0001t0020 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1530 | chr12 | 96953583 | ||||||
| chr12:96953727 | A | G | 1 | a0001c0001t0013 | 2 | HG02647.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1674A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1674 | chr12 | 96953727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96907335 | C | T | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-262+35C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907335 | |||||||
| chr12:96907362 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-262+62G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907362 | |||||||
| chr12:96907456 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-261-148G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907456 | |||||||
| chr12:96908203 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+347A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908203 | |||||||
| chr12:96908255 | A | G | 1 | a0001c0001t0002g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9+399A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908255 | |||||||
| chr12:96908420 | AG | A | 5 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(2): Show |
6 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+566delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96908420 | ||||||
| chr12:96908535 | T | C | 315 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(312): Show |
382 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(379): Show |
intron_variant | MODIFIER | c.-9+679T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908535 | |||||||
| chr12:96908595 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-9+739T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908595 | |||||||
| chr12:96908616 | G | A | 7 | a0001c0001t0006g0046 a0001c0001t0006g0047 a0001c0001t0006g0048 others(4): Show |
7 | HG02965.hp2 HG03098.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+760G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908616 | |||||||
| chr12:96908704 | T | G | 1 | a0001c0001t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9+848T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908704 | |||||||
| chr12:96908810 | G | T | 1 | a0001c0001t0001g0036 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-8-942G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908810 | |||||||
| chr12:96908849 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-8-903T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908849 | |||||||
| chr12:96908871 | G | T | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8-881G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908871 | |||||||
| chr12:96908897 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-8-855C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908897 | |||||||
| chr12:96908905 | G | A | 119 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(116): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-8-847G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908905 | |||||||
| chr12:96908947 | C | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-805C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908947 | |||||||
| chr12:96908966 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-786C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908966 | |||||||
| chr12:96909021 | A | G | 1 | a0003c0008t0007g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-731A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909021 | |||||||
| chr12:96909142 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-610C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909142 | |||||||
| chr12:96909176 | C | CA | 170 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(167): Show |
212 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.-8-558dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | ||||||
| chr12:96909176 | C | CAA | 9 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0001c0001t0001g0293 others(6): Show |
9 | HG00642.hp2 HG01891.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-559_-8-558dupAA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | ||||||
| chr12:96909176 | CA | C | 10 | a0001c0001t0001g0329 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
10 | HG01243.hp2 HG01257.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-558delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | ||||||
| chr12:96909187 | A | T | 3 | a0001c0001t0006g0046 a0001c0001t0006g0047 a0001c0001t0006g0048 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-565A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909187 | |||||||
| chr12:96909197 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-555C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909197 | |||||||
| chr12:96909468 | A | G | 6 | a0001c0001t0005g0272 a0001c0001t0005g0273 a0001c0001t0005g0274 others(3): Show |
6 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-284A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909468 | |||||||
| chr12:96909501 | A | AG | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-249dupG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909501 | ||||||
| chr12:96909639 | T | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18944.hp2 NA18965.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-113T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909639 | |||||||
| chr12:96909744 | A | G | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(115): Show |
140 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(137): Show |
splice_region_variant&intron_variant | LOW | c.-8-8A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909744 | |||||||
| chr12:96909904 | T | TA | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0011g0009 others(2): Show |
7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+21dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96909904 | ||||||
| chr12:96909904 | TA | T | 95 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0003 others(92): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.136+21delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96909904 | ||||||
| chr12:96909913 | A | C | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(2): Show |
5 | HG00323.hp2 HG01192.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+18A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909913 | |||||||
| chr12:96909915 | A | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0142 a0001c0001t0002g0144 others(8): Show |
14 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+20A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909915 | |||||||
| chr12:96909917 | C | A | 1 | a0001c0001t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136+22C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909917 | |||||||
| chr12:96909966 | A | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.136+71A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909966 | |||||||
| chr12:96909970 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.136+75A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909970 | |||||||
| chr12:96910150 | A | C | 1 | a0001c0001t0002g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136+255A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910150 | |||||||
| chr12:96910230 | AAAT | A | 177 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(174): Show |
217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.136+339_136+341del others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96910230 | ||||||
| chr12:96910241 | A | G | 5 | a0001c0001t0006g0018 a0001c0001t0006g0284 a0001c0001t0006g0285 others(2): Show |
7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+346A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910241 | |||||||
| chr12:96910353 | C | T | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(203): Show |
253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.136+458C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910353 | |||||||
| chr12:96910659 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.136+764G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910659 | |||||||
| chr12:96910686 | A | G | 91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(88): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.136+791A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910686 | |||||||
| chr12:96910826 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.136+931C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910826 | |||||||
| chr12:96910934 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18944.hp2 NA18965.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1039G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910934 | |||||||
| chr12:96911273 | CTT | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.136+1381_136+1382d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96911273 | ||||||
| chr12:96911345 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-1378G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911345 | |||||||
| chr12:96911560 | C | T | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.137-1163C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911560 | |||||||
| chr12:96911776 | G | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-947G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911776 | |||||||
| chr12:96911802 | A | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0137 a0001c0001t0018g0138 |
4 | HG00597.hp1 NA18983.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-921A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911802 | |||||||
| chr12:96912108 | TTACATTT others(2): Show |
T | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.137-613_137-605del others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96912108 | ||||||
| chr12:96912188 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.137-535G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912188 | |||||||
| chr12:96912247 | A | G | 2 | a0001c0001t0004g0070 a0001c0001t0004g0071 |
2 | NA18954.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.137-476A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912247 | |||||||
| chr12:96912475 | C | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-248C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912475 | |||||||
| chr12:96912661 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-62T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912661 | |||||||
| chr12:96912825 | AT | A | 7 | a0001c0001t0001g0202 a0001c0001t0001g0319 a0001c0001t0001g0320 others(4): Show |
7 | HG02976.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+22delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96912825 | ||||||
| chr12:96912840 | A | T | 1 | a0001c0001t0004g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.231+23A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96912840 | |||||||
| chr12:96912848 | A | T | 7 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0273 others(4): Show |
7 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+31A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96912848 | |||||||
| chr12:96913257 | A | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(114): Show |
139 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.231+440A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913257 | |||||||
| chr12:96913357 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.231+540C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913357 | |||||||
| chr12:96913374 | C | CT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0034 others(18): Show |
28 | HG00558.hp2 HG02015.hp1 HG02027.hp2 others(25): Show |
intron_variant | MODIFIER | c.231+569dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913374 | ||||||
| chr12:96913404 | C | G | 1 | a0001c0001t0005g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231+587C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913404 | |||||||
| chr12:96913404 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG03669.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.231+587C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913404 | |||||||
| chr12:96913452 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.231+635C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913452 | |||||||
| chr12:96913484 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.231+667C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913484 | |||||||
| chr12:96913574 | A | G | 2 | a0001c0001t0004g0068 a0001c0001t0006g0283 |
2 | HG03453.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.231+757A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913574 | |||||||
| chr12:96913589 | G | A | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.231+772G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913589 | |||||||
| chr12:96913643 | A | T | 3 | a0001c0001t0007g0049 a0001c0001t0014g0050 a0001c0001t0014g0051 |
3 | HG02965.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.231+826A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913643 | |||||||
| chr12:96913726 | C | T | 1 | a0001c0001t0016g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.231+909C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913726 | |||||||
| chr12:96913755 | ATTTC | A | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.231+942_231+945del others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913755 | ||||||
| chr12:96913808 | C | CT | 21 | a0001c0001t0001g0255 a0001c0001t0004g0002 a0001c0001t0004g0008 others(18): Show |
27 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.231+1001dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913808 | ||||||
| chr12:96913866 | A | T | 1 | a0001c0001t0001g0007 | 4 | NA18942.hp1 NA19054.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+1049A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913866 | |||||||
| chr12:96913877 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231+1060C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913877 | |||||||
| chr12:96914204 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.231+1387G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914204 | |||||||
| chr12:96914411 | A | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+1594A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914411 | |||||||
| chr12:96914470 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.231+1653A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914470 | |||||||
| chr12:96914785 | T | A | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(202): Show |
252 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.231+1968T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914785 | |||||||
| chr12:96914893 | T | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+2076T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914893 | |||||||
| chr12:96914957 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.231+2140A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914957 | |||||||
| chr12:96915113 | A | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0196 |
3 | NA18968.hp1 NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.231+2296A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915113 | |||||||
| chr12:96915235 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.232-2386C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915235 | |||||||
| chr12:96915273 | C | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-2348C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915273 | |||||||
| chr12:96915901 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232-1720T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915901 | |||||||
| chr12:96916084 | T | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-1537T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916084 | |||||||
| chr12:96916127 | G | A | 1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.232-1494G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916127 | |||||||
| chr12:96916170 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232-1451C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916170 | |||||||
| chr12:96916230 | T | TTTA | 84 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(81): Show |
95 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.232-1361_232-1359d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | ||||||
| chr12:96916230 | T | TTTATTA | 59 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(56): Show |
76 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.232-1364_232-1359d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | ||||||
| chr12:96916230 | T | TTTATTAT others(2): Show |
22 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0001g0176 others(19): Show |
32 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.232-1367_232-1359d others(11): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | ||||||
| chr12:96916230 | T | TTTATTAT others(5): Show |
6 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
6 | HG00642.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1370_232-1359d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | ||||||
| chr12:96916230 | TTTA | T | 12 | a0001c0001t0002g0078 a0001c0001t0002g0133 a0001c0001t0002g0134 others(9): Show |
14 | HG01106.hp1 HG01515.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.232-1361_232-1359d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | ||||||
| chr12:96916262 | T | TATTATTA others(3): Show |
1 | a0001c0001t0001g0295 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.232-1359_232-1358i others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916262 | |||||||
| chr12:96916263 | T | A | 1 | a0001c0001t0023g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.232-1358T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916263 | |||||||
| chr12:96916302 | T | C | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.232-1319T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916302 | |||||||
| chr12:96916321 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232-1300C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916321 | |||||||
| chr12:96916322 | G | A | 1 | a0001c0001t0008g0205 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.232-1299G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916322 | |||||||
| chr12:96916389 | A | G | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232-1232A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916389 | |||||||
| chr12:96916476 | A | G | 2 | a0002c0003t0003g0180 a0002c0003t0003g0181 |
2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.232-1145A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916476 | |||||||
| chr12:96916492 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.232-1129G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916492 | |||||||
| chr12:96916534 | C | T | 1 | a0003c0008t0007g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.232-1087C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916534 | |||||||
| chr12:96916582 | A | G | 2 | a0001c0002t0010g0076 a0001c0002t0010g0077 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.232-1039A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916582 | |||||||
| chr12:96916613 | C | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0271 |
3 | HG00423.hp1 NA18971.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.232-1008C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916613 | |||||||
| chr12:96916705 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232-916G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916705 | |||||||
| chr12:96916774 | CATG | C | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-844_232-842del others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916774 | ||||||
| chr12:96916975 | G | T | 1 | a0001c0001t0007g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232-646G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916975 | |||||||
| chr12:96917053 | A | T | 3 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0179 |
3 | NA18950.hp2 NA18995.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.232-568A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917053 | |||||||
| chr12:96917380 | T | C | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-241T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917380 | |||||||
| chr12:96917485 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232-136T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917485 | |||||||
| chr12:96917598 | CT | C | 205 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(202): Show |
252 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
splice_region_variant&intron_variant | LOW | c.232-7delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96917598 | ||||||
| chr12:96917763 | T | C | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(193): Show |
242 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.348+26T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917763 | |||||||
| chr12:96917781 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.348+44A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917781 | |||||||
| chr12:96917806 | T | G | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+69T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917806 | |||||||
| chr12:96917837 | G | C | 1 | a0001c0001t0004g0058 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.348+100G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917837 | |||||||
| chr12:96917863 | G | A | 17 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0024 others(14): Show |
27 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+126G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917863 | |||||||
| chr12:96918043 | C | T | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.348+306C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918043 | |||||||
| chr12:96918177 | T | G | 21 | a0001c0001t0001g0207 a0001c0001t0004g0002 a0001c0001t0004g0008 others(18): Show |
27 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+440T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918177 | |||||||
| chr12:96918179 | G | T | 1 | a0001c0001t0006g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.348+442G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918179 | |||||||
| chr12:96918203 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.348+466C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918203 | |||||||
| chr12:96918401 | TAATATGA others(2): Show |
T | 175 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(172): Show |
215 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.348+670_348+678del others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 96918401 | ||||||
| chr12:96918500 | G | A | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.348+763G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918500 | |||||||
| chr12:96918512 | T | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.348+775T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918512 | |||||||
| chr12:96918556 | G | A | 1 | a0005c0004t0008g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.348+819G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918556 | |||||||
| chr12:96918699 | A | G | 18 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(15): Show |
24 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.348+962A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918699 | |||||||
| chr12:96918786 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.348+1049T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918786 | |||||||
| chr12:96918805 | T | C | 6 | a0001c0002t0010g0074 a0001c0002t0010g0075 a0001c0002t0010g0076 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+1068T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918805 | |||||||
| chr12:96918851 | C | T | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1114C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918851 | |||||||
| chr12:96919169 | C | T | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-816C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919169 | |||||||
| chr12:96919266 | G | T | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-719G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919266 | |||||||
| chr12:96919310 | T | TA | 8 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0273 others(5): Show |
8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-674dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 96919310 | ||||||
| chr12:96919473 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.349-512C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919473 | |||||||
| chr12:96919557 | T | A | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-428T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919557 | |||||||
| chr12:96919753 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.349-232T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919753 | |||||||
| chr12:96919808 | C | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0328 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.349-177C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919808 | |||||||
| chr12:96919809 | G | A | 1 | a0001c0001t0015g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.349-176G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919809 | |||||||
| chr12:96920191 | C | T | 4 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+66C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920191 | |||||||
| chr12:96920223 | A | G | 83 | a0001c0001t0001g0168 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.489+98A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920223 | |||||||
| chr12:96920306 | A | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+181A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920306 | |||||||
| chr12:96920395 | A | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+270A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920395 | |||||||
| chr12:96920571 | A | G | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(193): Show |
242 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.489+446A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920571 | |||||||
| chr12:96920636 | T | C | 1 | a0001c0001t0006g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+511T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920636 | |||||||
| chr12:96920855 | A | G | 1 | a0001c0001t0003g0179 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.489+730A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920855 | |||||||
| chr12:96920924 | CTT | C | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+804_489+805del others(2): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96920924 | ||||||
| chr12:96921047 | T | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+922T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921047 | |||||||
| chr12:96921467 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+1342C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921467 | |||||||
| chr12:96921533 | C | G | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+1408C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921533 | |||||||
| chr12:96921662 | A | ATT | 165 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(162): Show |
203 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.489+1547_489+1548d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921662 | ||||||
| chr12:96921662 | A | ATTT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0200 a0001c0001t0006g0018 others(8): Show |
13 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+1546_489+1548d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921662 | ||||||
| chr12:96921775 | A | AT | 102 | a0001c0001t0001g0168 a0001c0001t0001g0248 a0001c0001t0001g0269 others(99): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.489+1667dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921775 | ||||||
| chr12:96921775 | AT | A | 47 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+1667delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921775 | ||||||
| chr12:96921873 | C | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
14 | HG00423.hp2 HG00558.hp1 NA18946.hp1 others(11): Show |
intron_variant | MODIFIER | c.489+1748C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921873 | |||||||
| chr12:96922079 | G | A | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(202): Show |
252 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.489+1954G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922079 | |||||||
| chr12:96922308 | A | AG | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(193): Show |
242 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.489+2184dupG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96922308 | ||||||
| chr12:96922315 | C | T | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.489+2190C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922315 | |||||||
| chr12:96922384 | A | C | 1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+2259A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922384 | |||||||
| chr12:96922396 | T | A | 1 | a0001c0001t0007g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489+2271T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922396 | |||||||
| chr12:96922503 | A | G | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2378A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922503 | |||||||
| chr12:96922681 | C | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.489+2556C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922681 | |||||||
| chr12:96922730 | G | A | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.489+2605G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922730 | |||||||
| chr12:96922845 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0130 |
2 | NA18960.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.489+2720C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922845 | |||||||
| chr12:96923121 | GA | G | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+3006delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923121 | ||||||
| chr12:96923134 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489+3009A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923134 | |||||||
| chr12:96923186 | G | A | 3 | a0001c0001t0007g0049 a0001c0001t0014g0050 a0001c0001t0014g0051 |
3 | HG02965.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+3061G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923186 | |||||||
| chr12:96923214 | A | C | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3089A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923214 | |||||||
| chr12:96923214 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.489+3089A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923214 | |||||||
| chr12:96923314 | T | C | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(202): Show |
252 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.489+3189T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923314 | |||||||
| chr12:96923315 | G | A | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3190G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923315 | |||||||
| chr12:96923349 | CAT | C | 49 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0011 others(46): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.489+3225_489+3226d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923349 | |||||||
| chr12:96923358 | A | G | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3233A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923358 | |||||||
| chr12:96923552 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0163 a0001c0001t0017g0266 |
4 | NA18963.hp2 NA18983.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3427G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923552 | |||||||
| chr12:96923594 | T | A | 1 | a0001c0001t0001g0036 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.489+3469T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923594 | |||||||
| chr12:96923657 | G | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+3532G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923657 | |||||||
| chr12:96923663 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+3538T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923663 | |||||||
| chr12:96923669 | G | A | 49 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0207 others(46): Show |
65 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.489+3544G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923669 | |||||||
| chr12:96923699 | T | C | 1 | a0001c0001t0006g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+3574T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923699 | |||||||
| chr12:96923780 | A | G | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3655A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923780 | |||||||
| chr12:96923784 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0002g0088 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.489+3662_489+3663i others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923784 | ||||||
| chr12:96923787 | TTTGTGTG others(4): Show |
T | 1 | a0001c0001t0001g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.489+3664_489+3674d others(13): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923787 | ||||||
| chr12:96923788 | T | G | 1 | a0001c0001t0002g0088 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.489+3663T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | |||||||
| chr12:96923788 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0002g0092 a0001c0001t0002g0121 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.489+3663_489+3664i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | |||||||
| chr12:96923788 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0002g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+3663_489+3664i others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | |||||||
| chr12:96923788 | T | TTG | 13 | a0001c0001t0004g0055 a0001c0001t0004g0058 a0001c0001t0004g0063 others(10): Show |
13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3704_489+3705d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTG | 6 | a0001c0001t0002g0112 a0001c0001t0002g0123 a0001c0001t0002g0139 others(3): Show |
7 | HG00280.hp1 HG01433.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+3702_489+3705d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTG | 16 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0020 others(13): Show |
21 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+3700_489+3705d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0001t0002g0078 others(9): Show |
13 | HG00408.hp1 HG00438.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3698_489+3705d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTGT others(3): Show |
26 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(23): Show |
26 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+3696_489+3705d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTGT others(5): Show |
22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0023 others(19): Show |
23 | HG00621.hp2 HG00673.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.489+3694_489+3705d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTGT others(7): Show |
9 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0100 others(6): Show |
12 | HG00140.hp2 HG01123.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+3692_489+3705d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0002g0137 a0001c0001t0012g0097 |
2 | HG00597.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.489+3690_489+3705d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTG | T | 10 | a0001c0001t0002g0153 a0001c0001t0004g0002 a0001c0001t0004g0019 others(7): Show |
10 | HG01123.hp2 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3704_489+3705d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTG | T | 8 | a0001c0001t0004g0068 a0001c0001t0004g0070 a0001c0001t0014g0051 others(5): Show |
8 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3702_489+3705d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTG | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0007g0049 |
3 | HG02723.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.489+3700_489+3705d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTGT others(1): Show |
T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0199 a0001c0001t0001g0202 others(5): Show |
9 | HG00408.hp2 HG02698.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+3698_489+3705d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTGT others(3): Show |
T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(79): Show |
100 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.489+3696_489+3705d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTGT others(5): Show |
T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(69): Show |
90 | HG00558.hp2 HG01070.hp1 HG01099.hp2 others(87): Show |
intron_variant | MODIFIER | c.489+3694_489+3705d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTGT others(7): Show |
T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0218 a0001c0001t0001g0247 others(2): Show |
6 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+3692_489+3705d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923788 | TTGTGTGT others(9): Show |
T | 11 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(8): Show |
13 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3690_489+3705d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | ||||||
| chr12:96923850 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.489+3725G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923850 | |||||||
| chr12:96923995 | C | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0320 a0001c0001t0001g0324 others(1): Show |
5 | HG02109.hp2 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3870C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923995 | |||||||
| chr12:96924207 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0089 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.489+4082G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924207 | |||||||
| chr12:96924334 | T | G | 4 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+4209T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924334 | |||||||
| chr12:96924607 | T | A | 1 | a0001c0001t0004g0070 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.489+4482T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924607 | |||||||
| chr12:96924874 | A | G | 2 | a0001c0001t0001g0319 a0001c0001t0001g0323 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.489+4749A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924874 | |||||||
| chr12:96924924 | G | A | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+4799G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924924 | |||||||
| chr12:96924942 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489+4817G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924942 | |||||||
| chr12:96925136 | G | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0011g0009 others(2): Show |
7 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5011G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925136 | |||||||
| chr12:96925462 | C | T | 1 | a0001c0001t0009g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+5337C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925462 | |||||||
| chr12:96925505 | C | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0022 others(10): Show |
19 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+5380C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925505 | |||||||
| chr12:96925546 | A | G | 2 | a0001c0002t0010g0076 a0001c0002t0010g0077 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+5421A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925546 | |||||||
| chr12:96925658 | C | T | 1 | a0001c0001t0005g0272 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+5533C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925658 | |||||||
| chr12:96925660 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0247 |
3 | HG01257.hp1 HG01258.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.489+5535A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925660 | |||||||
| chr12:96925909 | A | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5784A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925909 | |||||||
| chr12:96926031 | A | AT | 6 | a0001c0001t0002g0316 a0001c0001t0007g0040 a0001c0001t0007g0312 others(3): Show |
7 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5917dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926031 | ||||||
| chr12:96926031 | A | ATT | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+5916_489+5917d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926031 | ||||||
| chr12:96926353 | A | G | 168 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(165): Show |
206 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.489+6228A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926353 | |||||||
| chr12:96926385 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.489+6260C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926385 | |||||||
| chr12:96926550 | AT | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+6439delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926550 | ||||||
| chr12:96926604 | T | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6479T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926604 | |||||||
| chr12:96926709 | G | A | 1 | a0001c0001t0005g0301 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.489+6584G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926709 | |||||||
| chr12:96926960 | C | A | 1 | a0001c0001t0004g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.489+6835C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926960 | |||||||
| chr12:96926987 | A | AATT | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6862_489+6863i others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926987 | |||||||
| chr12:96926988 | T | A | 4 | a0001c0001t0002g0091 a0001c0001t0002g0146 a0001c0001t0003g0185 others(1): Show |
4 | HG01168.hp1 HG01884.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6863T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926988 | |||||||
| chr12:96926988 | T | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6863T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926988 | |||||||
| chr12:96926988 | TTG | T | 265 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(262): Show |
325 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.489+6883_489+6884d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926988 | ||||||
| chr12:96926989 | TG | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0146 a0001c0001t0003g0185 others(1): Show |
4 | HG01168.hp1 HG01884.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6865delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926989 | |||||||
| chr12:96926994 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0206 a0001c0001t0001g0209 others(8): Show |
14 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+6869G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926994 | |||||||
| chr12:96927101 | C | G | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+6976C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927101 | |||||||
| chr12:96927143 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.489+7018A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927143 | |||||||
| chr12:96927293 | G | A | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+7168G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927293 | |||||||
| chr12:96927405 | A | G | 4 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+7280A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927405 | |||||||
| chr12:96927433 | C | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(202): Show |
252 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.489+7308C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927433 | |||||||
| chr12:96927908 | G | A | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.490-7068G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927908 | |||||||
| chr12:96928129 | A | T | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(173): Show |
216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.490-6847A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928129 | |||||||
| chr12:96928141 | A | G | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-6835A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928141 | |||||||
| chr12:96928179 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0107 a0001c0001t0002g0108 others(1): Show |
7 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-6797T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928179 | |||||||
| chr12:96928281 | T | C | 1 | a0001c0001t0008g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-6695T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928281 | |||||||
| chr12:96928292 | A | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-6684A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928292 | |||||||
| chr12:96928305 | A | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-6671A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928305 | |||||||
| chr12:96928402 | C | G | 1 | a0001c0001t0004g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.490-6574C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928402 | |||||||
| chr12:96928612 | G | A | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-6364G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928612 | |||||||
| chr12:96928681 | C | CT | 20 | a0001c0001t0001g0294 a0001c0001t0002g0056 a0001c0001t0002g0079 others(17): Show |
22 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-6272dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | ||||||
| chr12:96928681 | C | CTT | 16 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0055 others(13): Show |
21 | HG01934.hp1 HG01975.hp2 NA18612.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-6273_490-6272d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | ||||||
| chr12:96928681 | CT | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(118): Show |
145 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.490-6272delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | ||||||
| chr12:96928776 | T | A | 1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-6200T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928776 | |||||||
| chr12:96928926 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(76): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-6050G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928926 | |||||||
| chr12:96928969 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(98): Show |
120 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.490-6007C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928969 | |||||||
| chr12:96929341 | T | C | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-5635T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929341 | |||||||
| chr12:96929341 | TCTTAATG others(18): Show |
T | 193 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(190): Show |
238 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.490-5609_490-5585d others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929341 | ||||||
| chr12:96929356 | TTTTTTTT others(17): Show |
T | 12 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(9): Show |
14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-5610_490-5587d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929356 | ||||||
| chr12:96929465 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0186 a0001c0001t0003g0187 |
4 | HG00642.hp1 HG01255.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5511T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929465 | |||||||
| chr12:96929556 | T | TAC | 42 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0054 others(39): Show |
47 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.490-5376_490-5375d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | T | TACAC | 12 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0079 others(9): Show |
17 | HG01123.hp1 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-5378_490-5375d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TAC | T | 15 | a0001c0001t0001g0168 a0001c0001t0001g0329 a0001c0001t0002g0012 others(12): Show |
17 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-5376_490-5375d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACAC | T | 10 | a0001c0001t0001g0328 a0001c0001t0002g0105 a0001c0001t0002g0106 others(7): Show |
11 | HG01261.hp2 HG02004.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-5378_490-5375d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACAC | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
20 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-5380_490-5375d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(1): Show |
T | 17 | a0001c0001t0001g0327 a0001c0001t0003g0188 a0001c0001t0003g0198 others(14): Show |
17 | HG00741.hp1 HG01081.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-5382_490-5375d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(3): Show |
T | 15 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(12): Show |
18 | HG00642.hp2 HG01106.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-5384_490-5375d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0291 a0001c0001t0006g0048 a0001c0001t0007g0049 others(1): Show |
4 | HG03195.hp2 HG03239.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5386_490-5375d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(7): Show |
T | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(150): Show |
194 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.490-5388_490-5375d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(9): Show |
T | 14 | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0207 others(11): Show |
14 | HG02258.hp1 HG02622.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-5390_490-5375d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929556 | TACACACA others(11): Show |
T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-5392_490-5375d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | ||||||
| chr12:96929594 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-5382C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929594 | |||||||
| chr12:96929596 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5380C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929596 | |||||||
| chr12:96929597 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-5379A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929597 | |||||||
| chr12:96929598 | C | T | 17 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
20 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-5378C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929598 | |||||||
| chr12:96929599 | A | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5377A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929599 | |||||||
| chr12:96929600 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(133): Show |
166 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.490-5376C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929600 | |||||||
| chr12:96929601 | A | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
19 | HG00741.hp1 HG02109.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-5375A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929601 | |||||||
| chr12:96929603 | A | G | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(122): Show |
152 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.490-5373A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929603 | |||||||
| chr12:96929605 | G | A | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5371G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929605 | |||||||
| chr12:96929607 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(117): Show |
144 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.490-5369G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929607 | |||||||
| chr12:96929607 | G | GTA | 74 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(71): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.490-5353_490-5352d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929607 | ||||||
| chr12:96929607 | G | GTATA | 46 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0293 others(43): Show |
64 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.490-5355_490-5352d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929607 | ||||||
| chr12:96929622 | TA | T | 7 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0273 others(4): Show |
7 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-5353delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929622 | |||||||
| chr12:96929623 | A | AT | 5 | a0001c0001t0007g0040 a0001c0001t0007g0052 a0001c0001t0007g0312 others(2): Show |
6 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-5343dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | ||||||
| chr12:96929623 | A | ATATTT | 5 | a0001c0001t0006g0018 a0001c0001t0006g0284 a0001c0001t0006g0285 others(2): Show |
7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-5352_490-5351i others(7): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | ||||||
| chr12:96929623 | A | ATT | 6 | a0001c0001t0001g0200 a0001c0001t0002g0078 a0001c0001t0002g0146 others(3): Show |
6 | HG00323.hp2 HG01192.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-5344_490-5343d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | ||||||
| chr12:96929623 | A | T | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-5353A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929623 | |||||||
| chr12:96929623 | AT | A | 19 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(16): Show |
25 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-5343delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | ||||||
| chr12:96929624 | T | TA | 6 | a0001c0001t0001g0204 a0001c0001t0001g0237 a0001c0001t0004g0055 others(3): Show |
6 | HG02738.hp1 HG02922.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-5352_490-5351i others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929624 | |||||||
| chr12:96929625 | T | A | 143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(140): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.490-5351T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929625 | |||||||
| chr12:96929626 | T | A | 2 | a0001c0001t0001g0258 a0001c0001t0004g0059 |
2 | HG03669.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.490-5350T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929626 | |||||||
| chr12:96929627 | T | A | 8 | a0001c0001t0001g0168 a0001c0001t0002g0004 a0001c0001t0002g0107 others(5): Show |
11 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-5349T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929627 | |||||||
| chr12:96929647 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-5329T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929647 | |||||||
| chr12:96929723 | G | A | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-5253G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929723 | |||||||
| chr12:96929771 | GGACACAC | G | 9 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(6): Show |
11 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5204_490-5198d others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929771 | |||||||
| chr12:96929781 | TGGC | T | 9 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(6): Show |
11 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5194_490-5192d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929781 | |||||||
| chr12:96929946 | C | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
11 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5030C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929946 | |||||||
| chr12:96930156 | AAC | A | 6 | a0001c0001t0001g0168 a0001c0001t0005g0037 a0001c0001t0005g0272 others(3): Show |
7 | HG00140.hp1 HG00280.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-4765_490-4764d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACAC | A | 4 | a0001c0001t0002g0146 a0001c0001t0005g0274 a0001c0001t0005g0275 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4767_490-4764d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACAC | A | 4 | a0001c0001t0002g0145 a0001c0001t0005g0161 a0001c0001t0011g0073 others(1): Show |
4 | HG01515.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4769_490-4764d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(1): Show |
A | 8 | a0001c0001t0002g0092 a0001c0001t0002g0124 a0001c0001t0002g0128 others(5): Show |
8 | HG02148.hp1 HG02922.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-4771_490-4764d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(3): Show |
A | 24 | a0001c0001t0001g0291 a0001c0001t0002g0003 a0001c0001t0002g0010 others(21): Show |
32 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-4773_490-4764d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(5): Show |
A | 28 | a0001c0001t0001g0238 a0001c0001t0002g0011 a0001c0001t0002g0020 others(25): Show |
32 | HG00323.hp1 HG00673.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-4775_490-4764d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(7): Show |
A | 35 | a0001c0001t0001g0163 a0001c0001t0001g0213 a0001c0001t0001g0239 others(32): Show |
41 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-4777_490-4764d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(9): Show |
A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0210 others(14): Show |
19 | HG01069.hp2 HG01167.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4779_490-4764d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(11): Show |
A | 25 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0036 others(22): Show |
29 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-4781_490-4764d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(13): Show |
A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(47): Show |
64 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.490-4783_490-4764d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(15): Show |
A | 11 | a0001c0001t0001g0042 a0001c0001t0001g0200 a0001c0001t0001g0221 others(8): Show |
12 | HG01975.hp1 HG01978.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-4785_490-4764d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930156 | AACACACA others(17): Show |
A | 45 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0234 others(42): Show |
60 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.490-4787_490-4764d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | ||||||
| chr12:96930179 | ACACACAC others(33): Show |
A | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-4795_490-4756d others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930179 | ||||||
| chr12:96930183 | ACACACAC others(23): Show |
A | 1 | a0001c0001t0023g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-4791_490-4762d others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930183 | ||||||
| chr12:96930185 | ACACACAC others(33): Show |
A | 19 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(16): Show |
25 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-4789_490-4750d others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930185 | ||||||
| chr12:96930186 | CACACACA others(12): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-4789_490-4771d others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930186 | |||||||
| chr12:96930187 | ACACACAC others(19): Show |
A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0320 |
3 | HG02109.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-4787_490-4762d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | ||||||
| chr12:96930187 | ACACACAC others(21): Show |
A | 2 | a0001c0001t0006g0018 a0002c0003t0003g0180 |
2 | HG02572.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.490-4787_490-4760d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | ||||||
| chr12:96930187 | ACACACAC others(31): Show |
A | 1 | a0001c0001t0004g0066 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490-4787_490-4750d others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | ||||||
| chr12:96930189 | ACACACAC others(17): Show |
A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0319 a0001c0001t0001g0321 others(4): Show |
8 | HG00741.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-4785_490-4762d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | ||||||
| chr12:96930189 | ACACACAC others(19): Show |
A | 3 | a0001c0001t0001g0324 a0001c0001t0006g0018 a0001c0001t0006g0286 |
4 | HG01106.hp1 HG01928.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4785_490-4760d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | ||||||
| chr12:96930189 | ACACACAC others(21): Show |
A | 1 | a0001c0001t0006g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-4785_490-4758d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | ||||||
| chr12:96930191 | ACACACAC others(15): Show |
A | 1 | a0001c0001t0006g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.490-4783_490-4762d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | ||||||
| chr12:96930191 | ACACACAC others(19): Show |
A | 4 | a0001c0001t0006g0046 a0001c0001t0006g0047 a0001c0001t0006g0048 others(1): Show |
4 | HG02280.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4783_490-4758d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | ||||||
| chr12:96930191 | ACACACAC others(21): Show |
A | 1 | a0001c0006t0006g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-4783_490-4756d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | ||||||
| chr12:96930193 | A | T | 2 | a0001c0001t0002g0098 a0001c0001t0007g0052 |
2 | NA18747.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.490-4783A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930193 | |||||||
| chr12:96930193 | ACACACAC others(15): Show |
A | 1 | a0001c0001t0006g0292 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.490-4781_490-4760d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930193 | ||||||
| chr12:96930195 | A | T | 1 | a0001c0001t0007g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-4781A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930195 | |||||||
| chr12:96930195 | ACACACAC others(13): Show |
A | 1 | a0001c0001t0006g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.490-4779_490-4760d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930195 | ||||||
| chr12:96930195 | ACACACAC others(15): Show |
A | 1 | a0001c0001t0007g0040 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.490-4779_490-4758d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930195 | ||||||
| chr12:96930197 | A | T | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-4779A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930197 | |||||||
| chr12:96930197 | ACACACAC others(9): Show |
A | 2 | a0001c0001t0002g0154 a0001c0002t0010g0075 |
2 | HG01257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-4777_490-4762d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | ||||||
| chr12:96930197 | ACACACAC others(11): Show |
A | 1 | a0001c0001t0002g0118 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.490-4777_490-4760d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | ||||||
| chr12:96930197 | ACACACAC others(17): Show |
A | 1 | a0001c0001t0007g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-4777_490-4754d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | ||||||
| chr12:96930199 | A | T | 3 | a0001c0001t0001g0238 a0001c0001t0008g0222 a0001c0001t0009g0162 |
3 | HG01891.hp2 HG03654.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.490-4777A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930199 | |||||||
| chr12:96930199 | ACACACAC others(9): Show |
A | 1 | a0001c0001t0002g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.490-4775_490-4760d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930199 | ||||||
| chr12:96930199 | ACACACAC others(15): Show |
A | 2 | a0001c0001t0007g0049 a0001c0002t0010g0279 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-4775_490-4754d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930199 | ||||||
| chr12:96930201 | A | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0213 a0001c0001t0001g0238 others(7): Show |
10 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-4775A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930201 | |||||||
| chr12:96930201 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490-4773_490-4762d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | ||||||
| chr12:96930201 | ACACACAC others(7): Show |
A | 1 | a0001c0001t0007g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-4773_490-4760d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | ||||||
| chr12:96930201 | ACACACAC others(9): Show |
A | 2 | a0001c0001t0007g0312 a0001c0001t0007g0314 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.490-4773_490-4758d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | ||||||
| chr12:96930201 | ACACACAC others(13): Show |
A | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-4773_490-4754d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | ||||||
| chr12:96930203 | A | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0163 others(20): Show |
25 | HG01099.hp2 HG01109.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-4773A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930203 | |||||||
| chr12:96930205 | A | T | 35 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0032 others(32): Show |
41 | HG00408.hp2 HG01099.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-4771A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930205 | |||||||
| chr12:96930207 | A | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(94): Show |
117 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.490-4769A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930207 | |||||||
| chr12:96930209 | A | ACT | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0020g0167 |
3 | HG01891.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.490-4766_490-4765i others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930209 | ||||||
| chr12:96930209 | A | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(110): Show |
133 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.490-4767A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930209 | |||||||
| chr12:96930209 | ACACTCTC others(5): Show |
A | 1 | a0001c0002t0010g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.490-4765_490-4754d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930209 | ||||||
| chr12:96930211 | A | T | 151 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(148): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.490-4765A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930211 | |||||||
| chr12:96930243 | T | A | 22 | a0001c0001t0001g0214 a0001c0001t0004g0002 a0001c0001t0004g0008 others(19): Show |
28 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.490-4733T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930243 | |||||||
| chr12:96930245 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.490-4731A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930245 | |||||||
| chr12:96930557 | G | A | 2 | a0001c0002t0010g0074 a0001c0002t0010g0075 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.490-4419G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930557 | |||||||
| chr12:96930557 | G | C | 1 | a0001c0001t0003g0178 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490-4419G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930557 | |||||||
| chr12:96930633 | C | T | 1 | a0001c0001t0008g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-4343C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930633 | |||||||
| chr12:96930700 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(76): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-4276G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930700 | |||||||
| chr12:96930784 | A | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-4192A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930784 | |||||||
| chr12:96930848 | A | G | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(202): Show |
252 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.490-4128A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930848 | |||||||
| chr12:96930960 | A | G | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-4016A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930960 | |||||||
| chr12:96930981 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0297 |
2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.490-3995T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930981 | |||||||
| chr12:96931355 | A | G | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-3621A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931355 | |||||||
| chr12:96931414 | A | T | 1 | a0001c0001t0008g0205 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.490-3562A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931414 | |||||||
| chr12:96931449 | T | A | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.490-3527T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931449 | |||||||
| chr12:96931755 | A | AGTAT | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-3219_490-3216d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96931755 | ||||||
| chr12:96931786 | A | G | 2 | a0001c0001t0005g0276 a0001c0001t0005g0277 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-3190A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931786 | |||||||
| chr12:96931894 | C | G | 1 | a0001c0001t0012g0097 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490-3082C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931894 | |||||||
| chr12:96931911 | T | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0202 a0001c0001t0001g0226 others(3): Show |
7 | HG02004.hp2 HG02129.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-3065T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931911 | |||||||
| chr12:96932145 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.490-2831A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932145 | |||||||
| chr12:96932166 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(79): Show |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.490-2810G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932166 | |||||||
| chr12:96932190 | T | C | 1 | a0001c0001t0002g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490-2786T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932190 | |||||||
| chr12:96932440 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2536C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932440 | |||||||
| chr12:96932442 | T | TA | 6 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0276 others(3): Show |
6 | HG02071.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2512dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932442 | ||||||
| chr12:96932443 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.490-2533A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932443 | |||||||
| chr12:96932444 | A | C | 2 | a0001c0002t0010g0279 a0001c0002t0010g0280 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.490-2532A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932444 | |||||||
| chr12:96932455 | A | AATATATA others(11): Show |
1 | a0001c0001t0002g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.490-2520_490-2519i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | ||||||
| chr12:96932455 | A | AATATATA others(17): Show |
1 | a0001c0001t0002g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.490-2520_490-2519i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | ||||||
| chr12:96932455 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-2520_490-2519i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | ||||||
| chr12:96932455 | A | AATATATA others(27): Show |
1 | a0001c0001t0018g0138 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.490-2520_490-2519i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | ||||||
| chr12:96932455 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 |
3 | HG01257.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.490-2519_490-2504d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | ||||||
| chr12:96932457 | A | AATATATA others(7): Show |
1 | a0001c0001t0002g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.490-2518_490-2517i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(9): Show |
5 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0078 others(2): Show |
5 | HG02818.hp2 NA18959.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(11): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
4 | HG00438.hp1 HG01167.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(13): Show |
6 | a0001c0001t0002g0013 a0001c0001t0002g0022 a0001c0001t0002g0084 others(3): Show |
7 | HG00673.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(15): Show |
7 | a0001c0001t0002g0012 a0001c0001t0002g0057 a0001c0001t0002g0123 others(4): Show |
7 | HG01433.hp1 HG01433.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(17): Show |
8 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0091 others(5): Show |
8 | HG01069.hp1 HG01243.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(19): Show |
7 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0054 others(4): Show |
7 | HG00597.hp1 HG01516.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(21): Show |
6 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0023 others(3): Show |
6 | HG00280.hp1 HG01123.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(25): Show |
3 | a0001c0001t0002g0128 a0001c0001t0002g0133 a0001c0001t0004g0085 |
3 | HG02148.hp1 NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.490-2518_490-2517i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | AATATATA others(31): Show |
1 | a0001c0001t0002g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-2518_490-2517i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | ||||||
| chr12:96932457 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(14): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0106 |
2 | NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(16): Show |
3 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0024g0080 |
3 | HG02615.hp1 NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0079 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(20): Show |
1 | a0001c0001t0002g0092 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0010 | 2 | NA19084.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | ATATATAT others(26): Show |
1 | a0001c0001t0012g0099 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-2519_490-2518i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932457 | A | T | 5 | a0001c0001t0002g0101 a0001c0001t0002g0113 a0001c0001t0002g0120 others(2): Show |
5 | HG00621.hp2 HG01106.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2519A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | |||||||
| chr12:96932459 | A | AATATATA others(7): Show |
1 | a0001c0001t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-2516_490-2515i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(9): Show |
1 | a0001c0001t0002g0011 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(13): Show |
1 | a0001c0001t0002g0130 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(15): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0131 |
2 | HG02723.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0114 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(21): Show |
3 | a0001c0001t0002g0094 a0001c0001t0002g0105 a0001c0001t0002g0118 |
3 | HG02004.hp2 NA18984.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(23): Show |
1 | a0001c0001t0002g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(25): Show |
2 | a0001c0001t0002g0116 a0001c0001t0015g0087 |
2 | NA19081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | AATATATA others(27): Show |
1 | a0001c0001t0002g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | ||||||
| chr12:96932459 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-2517_490-2516i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932459 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0121 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.490-2517_490-2516i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932459 | A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0004 | 3 | HG01256.hp1 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.490-2517_490-2516i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932459 | A | ATATATAT others(16): Show |
2 | a0001c0001t0002g0110 a0001c0001t0002g0141 |
2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.490-2517_490-2516i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932459 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.490-2517_490-2516i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932459 | A | T | 57 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(54): Show |
69 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.490-2517A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | |||||||
| chr12:96932461 | A | AATATATA others(15): Show |
1 | a0001c0001t0002g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490-2514_490-2513i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932461 | ||||||
| chr12:96932461 | A | AATATATA others(21): Show |
1 | a0001c0001t0002g0021 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.490-2514_490-2513i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932461 | ||||||
| chr12:96932461 | A | ATATATAT others(6): Show |
1 | a0001c0001t0013g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.490-2515_490-2514i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | |||||||
| chr12:96932461 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | |||||||
| chr12:96932461 | A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | |||||||
| chr12:96932461 | A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0088 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | |||||||
| chr12:96932461 | A | T | 74 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(71): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.490-2515A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | |||||||
| chr12:96932463 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0006g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0006g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(24): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0242 |
2 | HG02135.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0003g0005 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0006 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0243 |
2 | HG02056.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0006g0286 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0009g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0033 a0001c0001t0006g0046 |
3 | HG01257.hp1 HG01258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0262 a0001c0001t0001g0265 |
3 | HG01167.hp1 HG02027.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0252 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0220 |
2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(28): Show |
5 | a0001c0001t0001g0221 a0001c0001t0001g0241 a0001c0001t0001g0264 others(2): Show |
5 | HG01255.hp1 HG01975.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0004g0019 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(32): Show |
2 | a0001c0001t0004g0062 a0001c0001t0004g0152 |
2 | HG02148.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(34): Show |
1 | a0001c0001t0001g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(43): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0035 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0291 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(11): Show |
1 | a0001c0002t0010g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0006g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(15): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0327 |
4 | HG02109.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0329 a0001c0001t0002g0145 a0001c0001t0009g0016 |
3 | HG01515.hp2 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(21): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0233 a0001c0001t0001g0247 others(1): Show |
4 | HG00438.hp2 HG01978.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0165 |
2 | NA18955.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(25): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0204 others(4): Show |
7 | HG00408.hp2 HG01975.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(27): Show |
4 | a0001c0001t0001g0270 a0001c0001t0003g0159 a0001c0001t0003g0172 others(1): Show |
4 | HG00621.hp1 NA18946.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(29): Show |
5 | a0001c0001t0001g0217 a0001c0001t0001g0232 a0001c0001t0001g0254 others(2): Show |
5 | HG00673.hp2 HG01099.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0289 |
2 | HG01070.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(33): Show |
4 | a0001c0001t0001g0251 a0001c0001t0002g0146 a0001c0001t0003g0014 others(1): Show |
4 | HG00558.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(46): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0319 a0001c0001t0006g0018 |
2 | HG01928.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0324 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0017 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0007 a0001c0001t0003g0005 |
2 | NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(24): Show |
8 | a0001c0001t0001g0015 a0001c0001t0001g0207 a0001c0001t0001g0211 others(5): Show |
9 | HG02809.hp1 NA18945.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(26): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0219 a0001c0001t0002g0144 others(1): Show |
4 | HG01069.hp2 HG03017.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(28): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0176 a0001c0001t0003g0001 others(1): Show |
4 | HG01952.hp2 HG02300.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(30): Show |
3 | a0001c0001t0001g0006 a0001c0001t0002g0149 a0001c0001t0004g0058 |
3 | HG01192.hp1 HG02293.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(32): Show |
4 | a0001c0001t0001g0218 a0001c0001t0001g0245 a0001c0001t0001g0250 others(1): Show |
4 | HG00423.hp1 HG01081.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(34): Show |
2 | a0001c0001t0003g0001 a0001c0001t0003g0158 |
2 | NA19076.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(43): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(48): Show |
1 | a0001c0001t0001g0030 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(57): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0234 a0001c0001t0014g0051 |
2 | HG02965.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0320 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(15): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0225 a0001c0001t0001g0325 others(3): Show |
6 | HG02080.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(19): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0006g0048 |
3 | HG03195.hp2 NA18942.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0239 |
3 | NA18999.hp2 NA19068.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(23): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0163 others(3): Show |
6 | HG02083.hp2 NA19001.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(25): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0003g0001 others(1): Show |
5 | HG00738.hp1 HG02083.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(27): Show |
6 | a0001c0001t0001g0259 a0001c0001t0003g0014 a0001c0001t0003g0171 others(3): Show |
6 | HG01358.hp1 NA18959.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(29): Show |
5 | a0001c0001t0001g0293 a0001c0001t0003g0027 a0001c0001t0003g0196 others(2): Show |
5 | HG00423.hp2 HG00642.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(31): Show |
10 | a0001c0001t0001g0228 a0001c0001t0001g0249 a0001c0001t0001g0294 others(7): Show |
11 | HG01109.hp2 HG03540.hp2 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(33): Show |
2 | a0001c0001t0003g0189 a0001c0001t0004g0059 |
2 | HG00741.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0008g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(44): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(37): Show |
1 | a0001c0001t0003g0025 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(46): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(39): Show |
1 | a0001c0001t0009g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(48): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0007g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0031 a0001c0001t0001g0278 a0001c0001t0004g0002 |
3 | HG01934.hp1 HG02523.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0253 a0001c0001t0007g0040 |
2 | HG00609.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0323 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(20): Show |
4 | a0001c0001t0001g0166 a0001c0001t0001g0203 a0001c0001t0004g0069 others(1): Show |
4 | HG00609.hp1 HG02896.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(22): Show |
4 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0004g0008 others(1): Show |
4 | HG03098.hp1 NA18957.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(24): Show |
3 | a0001c0001t0003g0025 a0001c0001t0004g0002 a0001c0001t0008g0205 |
3 | HG01496.hp1 HG03490.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0209 a0001c0001t0001g0227 |
2 | HG01175.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(28): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0003g0001 others(3): Show |
6 | HG02080.hp1 HG02698.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0248 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(32): Show |
3 | a0001c0001t0001g0269 a0001c0001t0003g0187 a0001c0001t0004g0071 |
3 | HG01255.hp2 HG02602.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0014g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0043 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0003g0190 a0001c0001t0007g0314 |
2 | HG02897.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0002g0150 a0001c0001t0004g0002 a0001c0001t0008g0230 |
3 | HG02735.hp2 HG06807.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0296 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(25): Show |
8 | a0001c0001t0001g0044 a0001c0001t0001g0199 a0001c0001t0001g0240 others(5): Show |
8 | HG01168.hp1 HG02698.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(27): Show |
7 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0002g0153 others(4): Show |
7 | HG01243.hp2 HG02015.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0223 a0001c0001t0001g0290 a0001c0001t0003g0026 |
3 | HG00597.hp2 HG02071.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(31): Show |
3 | a0001c0001t0001g0017 a0001c0001t0004g0065 a0001c0001t0004g0070 |
3 | HG00558.hp2 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0008 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(6): Show |
1 | a0003c0008t0007g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0007g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0007g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0007g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(28): Show |
4 | a0001c0001t0001g0295 a0001c0001t0001g0297 a0001c0001t0002g0147 others(1): Show |
4 | HG00323.hp2 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(30): Show |
4 | a0001c0001t0003g0186 a0001c0002t0010g0074 a0001c0002t0010g0076 others(1): Show |
4 | HG01361.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0179 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0004g0063 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(27): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0317 a0001c0001t0004g0055 |
3 | HG02486.hp1 NA18975.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0003g0001 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0002 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAT others(24): Show |
1 | a0001c0001t0001g0231 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAAAT others(32): Show |
1 | a0001c0001t0001g0017 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0022g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAATA others(15): Show |
1 | a0001c0001t0006g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAAATA others(23): Show |
1 | a0005c0004t0008g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAAATAT others(28): Show |
1 | a0001c0002t0010g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAATATA others(21): Show |
3 | a0001c0001t0003g0183 a0001c0001t0003g0191 a0001c0001t0003g0193 |
3 | HG01099.hp1 HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAATATA others(25): Show |
1 | a0001c0001t0003g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAATATA others(19): Show |
1 | a0001c0001t0001g0258 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAAATATA others(21): Show |
1 | a0001c0001t0001g0257 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AAATATAT others(6): Show |
1 | a0001c0001t0013g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | AATATATA others(25): Show |
1 | a0001c0001t0001g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.490-2488_490-2487i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | ||||||
| chr12:96932463 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0098 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.490-2513_490-2512i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932463 | |||||||
| chr12:96932463 | A | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(76): Show |
97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490-2513A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932463 | |||||||
| chr12:96932464 | AT | A | 3 | a0001c0001t0005g0038 a0001c0001t0005g0308 a0001c0001t0020g0167 |
3 | HG01175.hp2 HG01261.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.490-2511delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932464 | |||||||
| chr12:96932465 | T | A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0274 a0001c0001t0005g0275 others(3): Show |
6 | HG01081.hp2 HG01192.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2511T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932465 | |||||||
| chr12:96932467 | T | A | 2 | a0001c0001t0005g0038 a0001c0001t0020g0167 |
2 | HG02572.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.490-2509T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932467 | |||||||
| chr12:96932471 | T | A | 1 | a0001c0006t0006g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2505T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932471 | |||||||
| chr12:96932473 | T | A | 1 | a0001c0006t0006g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2503T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932473 | |||||||
| chr12:96932480 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0124 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.490-2488_490-2487i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932480 | ||||||
| chr12:96932487 | T | A | 2 | a0001c0001t0002g0141 a0001c0006t0006g0287 |
2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.490-2489T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932487 | |||||||
| chr12:96932487 | T | TATATATA others(17): Show |
2 | a0001c0001t0002g0103 a0001c0001t0004g0083 |
2 | HG01515.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.490-2488_490-2487i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932487 | ||||||
| chr12:96932489 | A | G | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-2487A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932489 | |||||||
| chr12:96932489 | A | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0253 |
2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.490-2487A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932489 | |||||||
| chr12:96932491 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.490-2485A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932491 | |||||||
| chr12:96932529 | T | A | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2447T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932529 | |||||||
| chr12:96932546 | G | A | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.490-2430G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932546 | |||||||
| chr12:96932566 | T | TC | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.490-2408dupC | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932566 | ||||||
| chr12:96932587 | C | T | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2389C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932587 | |||||||
| chr12:96932588 | T | C | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2388T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932588 | |||||||
| chr12:96932599 | C | A | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2377C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932599 | |||||||
| chr12:96932733 | T | G | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2243T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932733 | |||||||
| chr12:96932883 | G | A | 315 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(312): Show |
382 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(379): Show |
intron_variant | MODIFIER | c.490-2093G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932883 | |||||||
| chr12:96932947 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-2029C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932947 | |||||||
| chr12:96932999 | C | CT | 23 | a0001c0001t0001g0241 a0001c0001t0002g0120 a0001c0001t0003g0174 others(20): Show |
29 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.490-1960dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932999 | ||||||
| chr12:96932999 | CT | C | 7 | a0001c0001t0001g0298 a0001c0001t0002g0104 a0001c0001t0002g0107 others(4): Show |
7 | HG01069.hp1 HG01099.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1960delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932999 | ||||||
| chr12:96933016 | TA | T | 4 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 others(1): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-1957delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96933016 | ||||||
| chr12:96933109 | A | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-1867A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933109 | |||||||
| chr12:96933136 | CTTG | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-1834_490-1832d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96933136 | ||||||
| chr12:96933190 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0247 |
3 | HG01257.hp1 HG01258.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.490-1786G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933190 | |||||||
| chr12:96933214 | A | T | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-1762A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933214 | |||||||
| chr12:96933236 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-1740C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933236 | |||||||
| chr12:96933336 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0237 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-1640C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933336 | |||||||
| chr12:96933367 | A | T | 1 | a0006c0007t0001g0246 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-1609A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933367 | |||||||
| chr12:96933475 | T | G | 3 | a0001c0001t0005g0274 a0001c0001t0005g0276 a0001c0001t0005g0277 |
3 | HG01192.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-1501T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933475 | |||||||
| chr12:96933816 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0100 |
2 | NA18963.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.490-1160G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933816 | |||||||
| chr12:96933829 | C | T | 5 | a0001c0001t0002g0057 a0001c0001t0002g0079 a0001c0001t0002g0100 others(2): Show |
5 | NA18950.hp1 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-1147C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933829 | |||||||
| chr12:96933849 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-1127C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933849 | |||||||
| chr12:96933985 | G | T | 1 | a0001c0001t0003g0187 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.490-991G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933985 | |||||||
| chr12:96934191 | A | G | 2 | a0001c0001t0005g0301 a0001c0001t0005g0309 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.490-785A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934191 | |||||||
| chr12:96934207 | C | CT | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(196): Show |
241 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.490-758dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96934207 | ||||||
| chr12:96934387 | T | C | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-589T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934387 | |||||||
| chr12:96934499 | T | C | 1 | a0003c0008t0007g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490-477T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934499 | |||||||
| chr12:96934501 | C | CT | 14 | a0001c0001t0001g0270 a0001c0001t0001g0318 a0001c0001t0006g0018 others(11): Show |
16 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-463dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96934501 | ||||||
| chr12:96934518 | C | A | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-458C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934518 | |||||||
| chr12:96934576 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.490-400C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934576 | |||||||
| chr12:96934592 | C | A | 177 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(174): Show |
217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.490-384C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934592 | |||||||
| chr12:96934593 | A | T | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-383A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934593 | |||||||
| chr12:96934671 | G | A | 4 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0065 others(1): Show |
4 | NA18970.hp1 NA19003.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-305G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934671 | |||||||
| chr12:96934936 | TGCTTATA others(1): Show |
T | 165 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(162): Show |
203 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.490-39_490-32delGC others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934936 | |||||||
| chr12:96935321 | A | G | 12 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(9): Show |
14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+116A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935321 | |||||||
| chr12:96935437 | G | A | 1 | a0001c0001t0019g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.719+232G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935437 | |||||||
| chr12:96935461 | C | A | 1 | a0001c0001t0022g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.719+256C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935461 | |||||||
| chr12:96935619 | A | T | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.719+414A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935619 | |||||||
| chr12:96935732 | A | T | 1 | a0001c0001t0002g0124 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.719+527A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935732 | |||||||
| chr12:96935755 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.719+550A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935755 | |||||||
| chr12:96935761 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.719+556C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935761 | |||||||
| chr12:96935834 | C | CAA | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.719+633_719+634dup others(2): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 96935834 | ||||||
| chr12:96935905 | G | GT | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.719+701dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 96935905 | ||||||
| chr12:96935935 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.720-676C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935935 | |||||||
| chr12:96935941 | G | C | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.720-670G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935941 | |||||||
| chr12:96936168 | A | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.720-443A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936168 | |||||||
| chr12:96936218 | A | G | 2 | a0001c0001t0003g0183 a0001c0001t0003g0191 |
2 | HG01099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.720-393A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936218 | |||||||
| chr12:96936290 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.720-321G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936290 | |||||||
| chr12:96936357 | G | C | 4 | a0001c0001t0007g0049 a0001c0001t0007g0052 a0001c0001t0014g0050 others(1): Show |
4 | HG02965.hp2 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-254G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936357 | |||||||
| chr12:96936391 | AG | A | 165 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(162): Show |
203 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.720-219delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936391 | |||||||
| chr12:96936525 | C | G | 1 | a0001c0001t0002g0112 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.720-86C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936525 | |||||||
| chr12:96936887 | C | CA | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+77dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 96936887 | ||||||
| chr12:96937023 | T | A | 1 | a0001c0001t0003g0196 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.922-175T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937023 | |||||||
| chr12:96937037 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.922-161A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937037 | |||||||
| chr12:96937047 | T | G | 8 | a0001c0001t0004g0019 a0001c0001t0004g0059 a0001c0001t0004g0060 others(5): Show |
9 | HG01123.hp2 HG01358.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.922-151T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937047 | |||||||
| chr12:96937065 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.922-133C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937065 | |||||||
| chr12:96937072 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.922-126G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937072 | |||||||
| chr12:96937137 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.922-61T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937137 | |||||||
| chr12:96937157 | CATT | C | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.922-39_922-37delTT others(1): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 96937157 | ||||||
| chr12:96937441 | GT | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1117+55delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96937441 | ||||||
| chr12:96937571 | A | G | 1 | a0001c0001t0020g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1117+178A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937571 | |||||||
| chr12:96937587 | A | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1117+194A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937587 | |||||||
| chr12:96937650 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1117+257G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937650 | |||||||
| chr12:96937882 | A | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+489A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937882 | |||||||
| chr12:96937926 | T | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(77): Show |
98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1117+533T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937926 | |||||||
| chr12:96938157 | C | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(87): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1117+764C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938157 | |||||||
| chr12:96938544 | G | A | 10 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(7): Show |
12 | HG01106.hp1 HG01884.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117+1151G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938544 | |||||||
| chr12:96938827 | TCTCTCTC others(3): Show |
T | 167 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(164): Show |
205 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.1117+1436_1117+144 others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96938827 | ||||||
| chr12:96938835 | T | TCA | 2 | a0001c0001t0005g0038 a0001c0001t0005g0308 |
3 | HG01175.hp2 HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1117+1455_1117+145 others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96938835 | ||||||
| chr12:96938847 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1117+1454A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938847 | |||||||
| chr12:96938858 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1117+1465T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938858 | |||||||
| chr12:96938924 | A | G | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1118-1485A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938924 | |||||||
| chr12:96938978 | T | A | 2 | a0001c0001t0004g0019 a0001c0001t0004g0151 |
3 | HG01123.hp2 HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1118-1431T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938978 | |||||||
| chr12:96939071 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1118-1338T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939071 | |||||||
| chr12:96939190 | G | C | 1 | a0001c0001t0002g0020 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1118-1219G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939190 | |||||||
| chr12:96939213 | G | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118-1196G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939213 | |||||||
| chr12:96939270 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1118-1139T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939270 | |||||||
| chr12:96939548 | T | A | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1118-861T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939548 | |||||||
| chr12:96939629 | A | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0109 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1118-780A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939629 | |||||||
| chr12:96939651 | T | A | 1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1118-758T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939651 | |||||||
| chr12:96939835 | A | G | 1 | a0001c0001t0009g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1118-574A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939835 | |||||||
| chr12:96939871 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1118-538T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939871 | |||||||
| chr12:96939947 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1118-462G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939947 | |||||||
| chr12:96940036 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1118-373T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96940036 | |||||||
| chr12:96940381 | A | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1118-28A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96940381 | |||||||
| chr12:96940667 | G | C | 2 | a0002c0003t0003g0180 a0002c0003t0003g0181 |
2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1246+130G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940667 | |||||||
| chr12:96940671 | T | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | NA18965.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1246+134T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940671 | |||||||
| chr12:96940742 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1246+205A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940742 | |||||||
| chr12:96940826 | C | T | 1 | a0001c0001t0023g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1246+289C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940826 | |||||||
| chr12:96940847 | A | G | 12 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(9): Show |
14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1246+310A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940847 | |||||||
| chr12:96940874 | G | A | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1246+337G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940874 | |||||||
| chr12:96940949 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1246+412T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940949 | |||||||
| chr12:96940953 | C | T | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1246+416C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940953 | |||||||
| chr12:96940994 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1246+457T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940994 | |||||||
| chr12:96941453 | T | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1246+916T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941453 | |||||||
| chr12:96941459 | G | A | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246+922G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941459 | |||||||
| chr12:96941572 | A | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(99): Show |
121 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1247-1005A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941572 | |||||||
| chr12:96941747 | C | CT | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1247-824dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 96941747 | ||||||
| chr12:96941804 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1247-773C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941804 | |||||||
| chr12:96941935 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1247-642T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941935 | |||||||
| chr12:96942649 | C | T | 4 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+25C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942649 | |||||||
| chr12:96942667 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG03669.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1294+43A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942667 | |||||||
| chr12:96942735 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1294+111G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942735 | |||||||
| chr12:96942905 | T | TA | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1294+282dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 96942905 | ||||||
| chr12:96942942 | G | A | 5 | a0001c0001t0006g0018 a0001c0001t0006g0284 a0001c0001t0006g0285 others(2): Show |
7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+318G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942942 | |||||||
| chr12:96942978 | C | T | 8 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0273 others(5): Show |
8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+354C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942978 | |||||||
| chr12:96943305 | T | C | 1 | a0001c0006t0006g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1295-255T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943305 | |||||||
| chr12:96943339 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1295-221A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943339 | |||||||
| chr12:96943404 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1295-156C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943404 | |||||||
| chr12:96943421 | G | A | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1295-139G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943421 | |||||||
| chr12:96943499 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1295-61T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943499 | |||||||
| chr12:96943818 | G | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1497+56G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943818 | |||||||
| chr12:96943832 | C | T | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(203): Show |
253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.1497+70C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943832 | |||||||
| chr12:96943918 | C | T | 47 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0293 others(44): Show |
63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1497+156C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943918 | |||||||
| chr12:96943956 | T | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1497+194T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943956 | |||||||
| chr12:96944057 | A | G | 1 | a0001c0001t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1497+295A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944057 | |||||||
| chr12:96944129 | C | G | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1497+367C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944129 | |||||||
| chr12:96944194 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1497+432A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944194 | |||||||
| chr12:96944227 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1498-412A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944227 | |||||||
| chr12:96944301 | T | A | 8 | a0001c0001t0001g0201 a0001c0001t0001g0257 a0001c0001t0001g0258 others(5): Show |
8 | HG03239.hp2 HG03490.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-338T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944301 | |||||||
| chr12:96944330 | G | A | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(203): Show |
253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.1498-309G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944330 | |||||||
| chr12:96944492 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(194): Show |
243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1498-147C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944492 | |||||||
| chr12:96944564 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0124 a0001c0001t0002g0129 |
5 | NA18959.hp1 NA18964.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-75A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944564 | |||||||
| chr12:96944818 | T | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1654+23T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944818 | |||||||
| chr12:96944829 | G | A | 6 | a0001c0002t0010g0074 a0001c0002t0010g0075 a0001c0002t0010g0076 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654+34G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944829 | |||||||
| chr12:96944904 | A | C | 1 | a0001c0001t0006g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1654+109A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944904 | |||||||
| chr12:96944918 | G | A | 194 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(191): Show |
240 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1654+123G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944918 | |||||||
| chr12:96945052 | T | G | 1 | a0001c0001t0020g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1654+257T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945052 | |||||||
| chr12:96945061 | TA | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1654+267delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945061 | |||||||
| chr12:96945081 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1654+286G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945081 | |||||||
| chr12:96945084 | T | G | 194 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(191): Show |
240 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1654+289T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945084 | |||||||
| chr12:96945142 | T | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1654+347T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945142 | |||||||
| chr12:96945150 | G | A | 315 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(312): Show |
382 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(379): Show |
intron_variant | MODIFIER | c.1654+355G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945150 | |||||||
| chr12:96945168 | C | G | 2 | a0001c0001t0014g0050 a0001c0001t0014g0051 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1654+373C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945168 | |||||||
| chr12:96945236 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1654+441A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945236 | |||||||
| chr12:96945265 | G | A | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(203): Show |
253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.1655-428G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945265 | |||||||
| chr12:96945458 | A | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(29): Show |
35 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1655-235A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945458 | |||||||
| chr12:96945487 | T | TTA | 7 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0159 others(4): Show |
11 | HG02027.hp1 HG02080.hp1 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.1655-197_1655-196d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 96945487 | ||||||
| chr12:96945610 | G | C | 307 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(304): Show |
374 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.1655-83G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945610 | |||||||
| chr12:96945908 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1811+59A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945908 | |||||||
| chr12:96945950 | G | A | 1 | a0001c0001t0008g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1811+101G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945950 | |||||||
| chr12:96945950 | G | T | 1 | a0001c0001t0002g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1811+101G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945950 | |||||||
| chr12:96946142 | A | C | 1 | a0001c0001t0003g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1811+293A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946142 | |||||||
| chr12:96946191 | A | G | 5 | a0001c0001t0006g0018 a0001c0001t0006g0284 a0001c0001t0006g0285 others(2): Show |
7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1811+342A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946191 | |||||||
| chr12:96946253 | A | G | 1 | a0001c0001t0003g0178 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1811+404A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946253 | |||||||
| chr12:96946273 | ATACT | A | 4 | a0001c0001t0007g0040 a0001c0001t0007g0312 a0001c0001t0007g0313 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1811+427_1811+430d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96946273 | ||||||
| chr12:96946283 | T | TA | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+442dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96946283 | ||||||
| chr12:96946300 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1811+451C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946300 | |||||||
| chr12:96946308 | T | C | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1811+459T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946308 | |||||||
| chr12:96946420 | T | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0223 a0001c0001t0001g0225 others(6): Show |
10 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+571T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946420 | |||||||
| chr12:96946740 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1811+891A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946740 | |||||||
| chr12:96946754 | G | A | 307 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(304): Show |
374 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.1811+905G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946754 | |||||||
| chr12:96946772 | A | G | 2 | a0001c0001t0013g0081 a0001c0001t0013g0082 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1811+923A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946772 | |||||||
| chr12:96946807 | G | A | 1 | a0001c0001t0003g0184 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1811+958G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946807 | |||||||
| chr12:96946826 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1811+977C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946826 | |||||||
| chr12:96947356 | A | G | 1 | a0001c0001t0021g0288 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1811+1507A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947356 | |||||||
| chr12:96947385 | G | A | 1 | a0001c0002t0010g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1811+1536G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947385 | |||||||
| chr12:96947422 | A | G | 1 | a0001c0001t0006g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1811+1573A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947422 | |||||||
| chr12:96947676 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0206 a0001c0001t0001g0217 others(2): Show |
8 | HG01070.hp1 HG01099.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1811+1827A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947676 | |||||||
| chr12:96947686 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1811+1837C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947686 | |||||||
| chr12:96947702 | C | A | 1 | a0001c0001t0012g0097 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1811+1853C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947702 | |||||||
| chr12:96947704 | T | C | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(203): Show |
253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.1811+1855T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947704 | |||||||
| chr12:96947765 | C | T | 3 | a0001c0001t0011g0009 a0001c0001t0011g0072 a0001c0001t0011g0073 |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1811+1916C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947765 | |||||||
| chr12:96947941 | G | A | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+2092G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947941 | |||||||
| chr12:96947955 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0323 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1811+2106C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947955 | |||||||
| chr12:96947956 | G | A | 1 | a0001c0001t0008g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1811+2107G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947956 | |||||||
| chr12:96948055 | A | G | 9 | a0001c0001t0007g0040 a0001c0001t0007g0049 a0001c0001t0007g0052 others(6): Show |
10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+2206A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948055 | |||||||
| chr12:96948418 | C | T | 9 | a0001c0001t0002g0142 a0001c0001t0002g0144 a0001c0001t0002g0145 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1811+2569C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948418 | |||||||
| chr12:96948578 | A | G | 151 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(148): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1811+2729A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948578 | |||||||
| chr12:96948581 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1811+2732A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948581 | |||||||
| chr12:96948649 | G | A | 13 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(10): Show |
16 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1812-2783G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948649 | |||||||
| chr12:96948714 | G | A | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-2718G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948714 | |||||||
| chr12:96948811 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1812-2621G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948811 | |||||||
| chr12:96948941 | G | A | 1 | a0001c0001t0005g0303 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1812-2491G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948941 | |||||||
| chr12:96949228 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1812-2204C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949228 | |||||||
| chr12:96949261 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1812-2171A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949261 | |||||||
| chr12:96949400 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1812-2032G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949400 | |||||||
| chr12:96949417 | A | T | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(89): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1812-2015A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949417 | |||||||
| chr12:96949731 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1812-1701A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949731 | |||||||
| chr12:96949736 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0089 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1812-1696C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949736 | |||||||
| chr12:96949951 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1812-1481C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949951 | |||||||
| chr12:96950055 | G | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-1377G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950055 | |||||||
| chr12:96950104 | A | C | 1 | a0001c0001t0004g0065 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1812-1328A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950104 | |||||||
| chr12:96950281 | C | T | 131 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(128): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1812-1151C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950281 | |||||||
| chr12:96950352 | T | C | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-1080T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950352 | |||||||
| chr12:96950371 | GTATACAC others(6): Show |
G | 2 | a0001c0002t0010g0279 a0001c0002t0010g0280 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1812-1058_1812-104 others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96950371 | ||||||
| chr12:96950540 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1812-892T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950540 | |||||||
| chr12:96950733 | G | A | 10 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(7): Show |
12 | HG01106.hp1 HG01884.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1812-699G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950733 | |||||||
| chr12:96951013 | T | C | 12 | a0001c0001t0006g0018 a0001c0001t0006g0046 a0001c0001t0006g0047 others(9): Show |
14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1812-419T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951013 | |||||||
| chr12:96951080 | C | T | 131 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(128): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1812-352C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951080 | |||||||
| chr12:96951145 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0019 others(17): Show |
26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-287C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951145 | |||||||
| chr12:96951206 | A | G | 1 | a0001c0001t0005g0161 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1812-226A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951206 | |||||||
| chr12:96951328 | A | G | 1 | a0001c0001t0005g0274 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1812-104A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951328 | |||||||
| chr12:96951594 | G | C | 1 | a0001c0001t0006g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1878+96G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951594 | |||||||
| chr12:96951636 | A | G | 5 | a0001c0001t0004g0008 a0001c0001t0004g0055 a0001c0001t0004g0058 others(2): Show |
7 | HG02148.hp2 NA18612.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878+138A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951636 | |||||||
| chr12:96951639 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1878+141A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951639 | |||||||
| chr12:96951702 | A | G | 2 | a0001c0001t0012g0096 a0001c0001t0012g0097 |
2 | NA18974.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1878+204A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951702 | |||||||
| chr12:96951763 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1879-186A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951763 | |||||||
| chr12:96951826 | A | G | 3 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 |
3 | HG01257.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1879-123A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951826 | |||||||
| chr12:96951873 | G | C | 8 | a0001c0001t0005g0161 a0001c0001t0005g0272 a0001c0001t0005g0273 others(5): Show |
8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1879-76G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951873 |