| geneid | 84955 |
|---|---|
| ensemblid | ENSG00000120526.12 |
| hgncid | 24306 |
| symbol | NUDCD1 |
| name | NudC domain containing 1 |
| refseq_nuc | NM_032869.4 |
| refseq_prot | NP_116258.2 |
| ensembl_nuc | ENST00000239690.9 |
| ensembl_prot | ENSP00000239690.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 109240919 |
| end | 109334087 |
| strand | - |
| ver | v1.2 |
| region | chr8:109240919-109334087 |
| region5000 | chr8:109235919-109339087 |
| regionname0 | NUDCD1_chr8_109240919_109334087 |
| regionname5000 | NUDCD1_chr8_109235919_109339087 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 583 | 126 | 17 | 27 | 69 | 7 | 6 | 54 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002 | 1/1 | 583 | 118 | 7 | 23 | 70 | 3 | 13 | 51 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003 | 0/0 | 583 | 83 | 52 | 13 | 9 | 2 | 7 | 7 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0004 | 0/0 | 583 | 14 | 0 | 1 | 0 | 2 | 11 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0005 | 0/0 | 583 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0006 | 0/0 | 583 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0007 | 0/0 | 583 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0008 | 0/0 | 583 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0009 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1752 | 126 | 17 | 27 | 69 | 7 | 6 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0002 | 1/1 | 1752 | 117 | 7 | 23 | 69 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0003 | 0/0 | 1752 | 82 | 51 | 13 | 9 | 2 | 7 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0004 | 0/0 | 1752 | 14 | 0 | 1 | 0 | 2 | 11 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0005 | 0/0 | 1752 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0006 | 0/0 | 1752 | 4 | 4 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0007 | 0/0 | 1752 | 3 | 0 | 0 | 0 | 0 | 3 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0008 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0009 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0010 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| c0011 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2171 | 131 | 17 | 27 | 67 | 7 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0002 | 1/1 | 2168 | 112 | 6 | 20 | 68 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0003 | 0/0 | 2172 | 38 | 14 | 8 | 9 | 2 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0004 | 0/0 | 2172 | 21 | 16 | 3 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0005 | 0/0 | 2172 | 12 | 11 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0006 | 0/0 | 2173 | 9 | 8 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0007 | 0/0 | 2173 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0008 | 0/0 | 2172 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0009 | 0/0 | 2171 | 6 | 0 | 0 | 0 | 1 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0010 | 0/0 | 2171 | 3 | 0 | 1 | 0 | 1 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0011 | 0/0 | 2168 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0012 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0013 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0014 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0015 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0016 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0017 | 0/0 | 2171 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0018 | 0/0 | 2171 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| t0019 | 0/0 | 2171 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0311 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1752 | 126 | 17 | 27 | 69 | 7 | 6 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002 | 1/1 | 1752 | 117 | 7 | 23 | 69 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0010 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003 | 0/0 | 1752 | 82 | 51 | 13 | 9 | 2 | 7 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0011 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0004c0004 | 0/0 | 1752 | 14 | 0 | 1 | 0 | 2 | 11 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0005c0005 | 0/0 | 1752 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0006c0006 | 0/0 | 1752 | 4 | 4 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0007c0007 | 0/0 | 1752 | 3 | 0 | 0 | 0 | 0 | 3 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0008c0008 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0009c0009 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3922 | 121 | 17 | 26 | 67 | 6 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0001c0001t0010 | 0/0 | 3922 | 3 | 0 | 1 | 0 | 1 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0001c0001t0018 | 0/0 | 3922 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0001c0001t0019 | 0/0 | 3922 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0002 | 1/1 | 3919 | 111 | 6 | 20 | 67 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0008 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0011 | 0/0 | 3919 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0014 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0015 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0002t0016 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0002c0010t0002 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0003 | 0/0 | 3923 | 36 | 12 | 8 | 9 | 2 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0004 | 0/0 | 3923 | 21 | 16 | 3 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0005 | 0/0 | 3923 | 12 | 11 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0006 | 0/0 | 3924 | 9 | 8 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0008 | 0/0 | 3923 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0003t0013 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0003c0011t0008 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0004c0004t0001 | 0/0 | 3922 | 8 | 0 | 1 | 0 | 1 | 6 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0004c0004t0009 | 0/0 | 3922 | 6 | 0 | 0 | 0 | 1 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0005c0005t0007 | 0/0 | 3924 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0006c0006t0008 | 0/0 | 3923 | 4 | 4 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0007c0007t0001 | 0/0 | 3922 | 2 | 0 | 0 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0007c0007t0017 | 0/0 | 3922 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0008c0008t0003 | 0/0 | 3923 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| a0009c0009t0012 | 0/0 | 3920 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | copy fasta | chr8 | 109235919 | 109339087 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0010g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0019g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0311 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0011g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0014g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0015g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0016g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0010t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0011t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0017g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0008c0008t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0008c0008t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0009c0009t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0261 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00140 | hp2 | a0004 | c0004 | t0001 | g0142 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00280 | hp1 | a0004 | c0004 | t0009 | g0165 | EUR | FIN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00558 | hp2 | a0002 | c0002 | t0011 | g0010 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00621 | hp2 | a0001 | c0001 | t0018 | g0073 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00639 | hp1 | a0003 | c0003 | t0003 | g0191 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0204 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0228 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00741 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00741 | hp2 | a0003 | c0003 | t0003 | g0209 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0275 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01099 | hp1 | a0002 | c0002 | t0016 | g0230 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0160 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01109 | hp1 | a0003 | c0003 | t0006 | g0027 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01167 | hp1 | a0003 | c0003 | t0005 | g0023 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0169 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01168 | hp1 | a0003 | c0003 | t0003 | g0185 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0241 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0216 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01243 | hp2 | a0002 | c0002 | t0015 | g0302 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01257 | hp1 | a0002 | c0002 | t0014 | g0220 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0304 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0305 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0007 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0264 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0303 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0184 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0229 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01516 | hp2 | a0003 | c0003 | t0003 | g0170 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0187 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0009 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01884 | hp2 | a0006 | c0006 | t0008 | g0336 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01891 | hp1 | a0005 | c0005 | t0007 | g0207 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01891 | hp2 | a0006 | c0006 | t0008 | g0335 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01934 | hp1 | a0003 | c0003 | t0004 | g0047 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0298 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0189 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0329 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0333 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0245 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0177 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02145 | hp1 | a0003 | c0003 | t0004 | g0341 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02145 | hp2 | a0005 | c0005 | t0007 | g0171 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | CDX | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02257 | hp1 | a0009 | c0009 | t0012 | g0048 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02257 | hp2 | a0003 | c0011 | t0008 | g0031 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02258 | hp2 | a0003 | c0003 | t0005 | g0001 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0195 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02280 | hp2 | a0005 | c0005 | t0007 | g0201 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02293 | hp1 | a0003 | c0003 | t0004 | g0045 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0221 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0260 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0036 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02615 | hp2 | a0003 | c0003 | t0005 | g0001 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02622 | hp2 | a0003 | c0003 | t0004 | g0345 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02630 | hp2 | a0003 | c0003 | t0006 | g0028 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0040 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02647 | hp2 | a0005 | c0005 | t0007 | g0172 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02683 | hp1 | a0004 | c0004 | t0009 | g0166 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02683 | hp2 | a0003 | c0003 | t0004 | g0046 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02698 | hp1 | a0003 | c0003 | t0003 | g0186 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0103 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02723 | hp1 | a0003 | c0003 | t0006 | g0212 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0034 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0307 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02738 | hp1 | a0004 | c0004 | t0001 | g0161 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0253 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02809 | hp2 | a0003 | c0003 | t0004 | g0214 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02818 | hp1 | a0003 | c0003 | t0005 | g0022 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02818 | hp2 | a0005 | c0005 | t0007 | g0173 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02886 | hp1 | a0003 | c0003 | t0004 | g0219 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0193 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02896 | hp2 | a0003 | c0003 | t0008 | g0033 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02897 | hp1 | a0003 | c0003 | t0008 | g0032 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02897 | hp2 | a0003 | c0003 | t0004 | g0218 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02965 | hp1 | a0003 | c0003 | t0013 | g0029 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02965 | hp2 | a0003 | c0003 | t0003 | g0037 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02970 | hp1 | a0006 | c0006 | t0008 | g0168 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0340 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02976 | hp1 | a0003 | c0003 | t0006 | g0026 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02976 | hp2 | a0003 | c0003 | t0004 | g0015 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03017 | hp1 | a0004 | c0004 | t0001 | g0162 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03017 | hp2 | a0007 | c0007 | t0017 | g0056 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0019 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03041 | hp2 | a0003 | c0003 | t0006 | g0343 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03098 | hp1 | a0008 | c0008 | t0003 | g0182 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03098 | hp2 | a0003 | c0003 | t0006 | g0009 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0247 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0192 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03195 | hp1 | a0003 | c0003 | t0004 | g0015 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03195 | hp2 | a0003 | c0003 | t0003 | g0039 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03209 | hp1 | a0003 | c0003 | t0005 | g0024 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03209 | hp2 | a0003 | c0003 | t0004 | g0217 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03225 | hp2 | a0005 | c0005 | t0007 | g0208 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03239 | hp1 | a0004 | c0004 | t0009 | g0164 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03239 | hp2 | a0007 | c0007 | t0001 | g0057 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03453 | hp1 | a0003 | c0003 | t0004 | g0213 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03453 | hp2 | a0005 | c0005 | t0007 | g0174 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03486 | hp1 | a0003 | c0003 | t0005 | g0025 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03486 | hp2 | a0003 | c0003 | t0006 | g0043 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0196 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03490 | hp2 | a0004 | c0004 | t0009 | g0008 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0309 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0141 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0308 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03492 | hp2 | a0004 | c0004 | t0009 | g0008 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03516 | hp1 | a0003 | c0003 | t0006 | g0042 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03516 | hp2 | a0006 | c0006 | t0008 | g0334 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03540 | hp1 | a0008 | c0008 | t0003 | g0197 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0339 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03579 | hp2 | a0003 | c0003 | t0004 | g0338 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0282 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03688 | hp2 | a0003 | c0003 | t0003 | g0175 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03710 | hp1 | a0007 | c0007 | t0001 | g0055 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0286 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03831 | hp1 | a0003 | c0003 | t0004 | g0044 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03831 | hp2 | a0004 | c0004 | t0001 | g0153 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03927 | hp1 | a0004 | c0004 | t0001 | g0062 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0205 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0312 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0283 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04199 | hp1 | a0004 | c0004 | t0009 | g0163 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04204 | hp1 | a0004 | c0004 | t0001 | g0140 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18522 | hp1 | a0003 | c0003 | t0005 | g0211 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0326 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18747 | hp2 | a0002 | c0010 | t0002 | g0291 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18906 | hp2 | a0003 | c0003 | t0004 | g0041 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18944 | hp1 | a0001 | c0001 | t0019 | g0084 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0176 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18970 | hp2 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18981 | hp1 | a0003 | c0003 | t0003 | g0181 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18985 | hp2 | a0003 | c0003 | t0003 | g0206 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0179 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0199 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0183 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0344 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19043 | hp1 | a0003 | c0003 | t0008 | g0030 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19043 | hp2 | a0003 | c0003 | t0003 | g0035 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19057 | hp2 | a0003 | c0003 | t0003 | g0180 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19065 | hp1 | a0002 | c0002 | t0011 | g0010 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0200 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ASW | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20129 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | ASW | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0007 | EUR | TSI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0240 | EUR | TSI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0194 | SAS | GIH | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0239 | SAS | GIH | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01123 | hp1 | a0003 | c0003 | t0003 | g0188 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02109 | hp1 | a0003 | c0003 | t0005 | g0018 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02109 | hp2 | a0005 | c0005 | t0007 | g0202 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0270 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02559 | hp2 | a0005 | c0005 | t0007 | g0203 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03471 | hp1 | a0003 | c0003 | t0005 | g0021 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03471 | hp2 | a0003 | c0003 | t0004 | g0215 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG06807 | hp1 | a0003 | c0003 | t0004 | g0337 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG06807 | hp2 | a0003 | c0003 | t0003 | g0190 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0198 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA21309 | hp2 | a0003 | c0003 | t0005 | g0017 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0311 | REF | REF | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0268 | REF | REF | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109271027
|
T | C | 1 | a0004 | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
missense_variant | MODERATE | c.1277A>G | p.Asn426Ser | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/10 | 1354/3919 | 1277/1752 | 426/583 | chr8 | 109271027 | ||
| chr8:109271124
|
T | G | 1 | a0004 | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
missense_variant | MODERATE | c.1180A>C | p.Asn394His | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/10 | 1257/3919 | 1180/1752 | 394/583 | chr8 | 109271124 | ||
| chr8:109275440
|
A | G | 1 | a0008 | 2 | HG03098.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.1085T>C | p.Ile362Thr | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/10 | 1162/3919 | 1085/1752 | 362/583 | chr8 | 109275440 | ||
| chr8:109289769
|
T | C | 3 | a0001a0004a0007 | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
missense_variant | MODERATE | c.805A>G | p.Ile269Val | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/10 | 882/3919 | 805/1752 | 269/583 | chr8 | 109289769 | ||
| chr8:109289818
|
T | G | 8 | a0001a0003a0004others(5): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
missense_variant | MODERATE | c.756A>C | p.Leu252Phe | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/10 | 833/3919 | 756/1752 | 252/583 | chr8 | 109289818 | ||
| chr8:109289906
|
C | T | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.668G>A | p.Arg223His | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/10 | 745/3919 | 668/1752 | 223/583 | chr8 | 109289906 | ||
| chr8:109293445
|
A | G | 1 | a0006 | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.539T>C | p.Ile180Thr | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/10 | 616/3919 | 539/1752 | 180/583 | chr8 | 109293445 | ||
| chr8:109296488
|
T | C | 1 | a0007 | 3 | HG03017.hp2 HG03239.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.355A>G | p.Ile119Val | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/10 | 432/3919 | 355/1752 | 119/583 | chr8 | 109296488 | ||
| chr8:109296547
|
C | T | 1 | a0005 | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
missense_variant | MODERATE | c.296G>A | p.Arg99Gln | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/10 | 373/3919 | 296/1752 | 99/583 | chr8 | 109296547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109275369
|
A | G | 1 | a0003c0011 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1156T>C | p.Leu386Leu | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/10 | 1233/3919 | 1156/1752 | 386/583 | chr8 | 109275369 | ||
| chr8:109281129
|
T | G | 1 | a0002c0010 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.867A>C | p.Val289Val | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/10 | 944/3919 | 867/1752 | 289/583 | chr8 | 109281129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109241012
|
C | T | 3 | a0003c0003t0004a0003c0003t0006a0009c0009t0012 | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1997 | chr8 | 109241012 | |||||
| chr8:109241073
|
T | C | 1 | a0002c0002t0014 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1936 | chr8 | 109241073 | |||||
| chr8:109241167
|
C | T | 1 | a0002c0002t0011 | 2 | HG00558.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1842G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1842 | chr8 | 109241167 | |||||
| chr8:109241269
|
T | C | 1 | a0002c0002t0015 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1740A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1740 | chr8 | 109241269 | |||||
| chr8:109241329
|
T | C | 1 | a0003c0003t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1680 | chr8 | 109241329 | |||||
| chr8:109241388
|
T | C | 1 | a0004c0004t0009 | 6 | HG00280.hp1 HG02683.hp1 HG03239.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1621A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1621 | chr8 | 109241388 | |||||
| chr8:109241553
|
C | T | 1 | a0007c0007t0017 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1456 | chr8 | 109241553 | |||||
| chr8:109241630
|
A | G | 1 | a0001c0001t0010 | 3 | HG01361.hp1 HG02698.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1379T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1379 | chr8 | 109241630 | |||||
| chr8:109241650
|
A | T | 10 | a0001c0001t0001a0001c0001t0010a0001c0001t0018others(7): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1359T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1359 | chr8 | 109241650 | |||||
| chr8:109241701
|
C | CTCTG | 19 | a0001c0001t0001a0001c0001t0010a0001c0001t0018others(16): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*1304_*1307dupCAGA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1307 | chr8 | 109241701 | |||||
| chr8:109241789
|
T | C | 1 | a0001c0001t0018 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1220A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1220 | chr8 | 109241789 | |||||
| chr8:109241928
|
T | C | 2 | a0003c0003t0003a0008c0008t0003 | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1081A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1081 | chr8 | 109241928 | |||||
| chr8:109241959
|
T | C | 1 | a0001c0001t0019 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1050A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 1050 | chr8 | 109241959 | |||||
| chr8:109242080
|
T | C | 1 | a0005c0005t0007 | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*929A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 929 | chr8 | 109242080 | |||||
| chr8:109242666
|
C | A | 8 | a0001c0001t0001a0001c0001t0010a0001c0001t0018others(5): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*343G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 343 | chr8 | 109242666 | |||||
| chr8:109242723
|
T | C | 1 | a0002c0002t0016 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 286 | chr8 | 109242723 | |||||
| chr8:109242786
|
C | CT | 3 | a0003c0003t0006a0005c0005t0007a0009c0009t0012 | 19 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*222dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 222 | chr8 | 109242786 | |||||
| chr8:109242786
|
CT | C | 8 | a0001c0001t0001a0001c0001t0010a0001c0001t0018others(5): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*222delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 10/10 | 222 | chr8 | 109242786 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109243367
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1460-66A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243367 | ||||||
| chr8:109243424
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1460-123A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243424 | ||||||
| chr8:109243579
|
A | G | 1 | a0003c0003t0004g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1460-278T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243579 | ||||||
| chr8:109243665
|
G | A | 5 | a0002c0002t0002g0232a0002c0002t0002g0267a0002c0002t0002g0271others(2): Show | 5 | HG00423.hp2 HG02155.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1460-364C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243665 | ||||||
| chr8:109243680
|
C | T | 1 | a0002c0002t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1460-379G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243680 | ||||||
| chr8:109243861
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1460-560A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109243861 | ||||||
| chr8:109244005
|
T | A | 1 | a0003c0003t0003g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1460-704A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244005 | ||||||
| chr8:109244123
|
CAATG | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1460-826_1460-823d others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244123 | ||||||
| chr8:109244339
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1459+983G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244339 | ||||||
| chr8:109244395
|
T | C | 1 | a0003c0003t0004g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1459+927A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244395 | ||||||
| chr8:109244452
|
G | C | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1459+870C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244452 | ||||||
| chr8:109244586
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1459+736T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244586 | ||||||
| chr8:109244623
|
C | T | 1 | a0003c0003t0004g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1459+699G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244623 | ||||||
| chr8:109244704
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1459+618T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109244704 | ||||||
| chr8:109245077
|
T | C | 16 | a0003c0003t0004g0015a0003c0003t0004g0213a0003c0003t0004g0214others(13): Show | 18 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1459+245A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109245077 | ||||||
| chr8:109245272
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1459+50T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 9/9 | chr8 | 109245272 | ||||||
| chr8:109245773
|
G | A | 38 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1300-292C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245773 | ||||||
| chr8:109245784
|
C | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-303G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245784 | ||||||
| chr8:109245946
|
T | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1300-465A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245946 | ||||||
| chr8:109245949
|
G | A | 38 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1300-468C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245949 | ||||||
| chr8:109245964
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-483A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245964 | ||||||
| chr8:109245988
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1300-507G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109245988 | ||||||
| chr8:109246289
|
C | T | 1 | a0002c0002t0002g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1300-808G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246289 | ||||||
| chr8:109246348
|
G | A | 2 | a0003c0003t0004g0219a0003c0003t0004g0341 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1300-867C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246348 | ||||||
| chr8:109246395
|
T | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-914A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246395 | ||||||
| chr8:109246436
|
T | C | 1 | a0002c0002t0002g0310 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1300-955A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246436 | ||||||
| chr8:109246584
|
T | G | 2 | a0003c0003t0004g0015a0003c0003t0004g0340 | 3 | HG02970.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1300-1103A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246584 | ||||||
| chr8:109246654
|
T | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-1173A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246654 | ||||||
| chr8:109246722
|
AC | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-1242delG | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246722 | ||||||
| chr8:109246724
|
A | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-1243T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246724 | ||||||
| chr8:109246739
|
T | C | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-1258A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246739 | ||||||
| chr8:109246816
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1300-1335C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246816 | ||||||
| chr8:109246864
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1300-1383G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109246864 | ||||||
| chr8:109247148
|
G | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1300-1667C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247148 | ||||||
| chr8:109247222
|
A | AT | 4 | a0003c0003t0004g0015a0003c0003t0004g0339a0003c0003t0004g0340others(1): Show | 5 | HG02970.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-1742dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247222 | ||||||
| chr8:109247307
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1300-1826A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247307 | ||||||
| chr8:109247391
|
C | T | 6 | a0005c0005t0007g0173a0005c0005t0007g0201a0005c0005t0007g0202others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-1910G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247391 | ||||||
| chr8:109247461
|
G | A | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-1980C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247461 | ||||||
| chr8:109247491
|
G | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-2010C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247491 | ||||||
| chr8:109247527
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-2046G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247527 | ||||||
| chr8:109247681
|
A | AT | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-2201dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247681 | ||||||
| chr8:109247696
|
T | C | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-2215A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247696 | ||||||
| chr8:109247762
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1300-2281C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247762 | ||||||
| chr8:109247781
|
G | C | 8 | a0002c0002t0002g0205a0002c0002t0002g0210a0002c0002t0002g0234others(5): Show | 8 | HG02083.hp1 HG03927.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1300-2300C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247781 | ||||||
| chr8:109247853
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300-2372A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247853 | ||||||
| chr8:109247887
|
C | T | 1 | a0003c0003t0003g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1300-2406G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247887 | ||||||
| chr8:109247932
|
TAA | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1300-2453_1300-245 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109247932 | ||||||
| chr8:109248053
|
G | T | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-2572C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248053 | ||||||
| chr8:109248314
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1300-2833T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248314 | ||||||
| chr8:109248340
|
C | T | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1300-2859G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248340 | ||||||
| chr8:109248418
|
C | T | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-2937G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248418 | ||||||
| chr8:109248419
|
T | C | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-2938A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248419 | ||||||
| chr8:109248420
|
C | T | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-2939G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248420 | ||||||
| chr8:109248514
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1300-3033C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248514 | ||||||
| chr8:109248714
|
G | GA | 40 | a0001c0001t0001g0052a0001c0001t0001g0077a0001c0001t0001g0092others(37): Show | 40 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1300-3234dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248714 | ||||||
| chr8:109248714
|
GA | G | 17 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0143others(14): Show | 18 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1300-3234delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248714 | ||||||
| chr8:109248749
|
A | C | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1300-3268T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248749 | ||||||
| chr8:109248804
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-3323G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248804 | ||||||
| chr8:109248893
|
C | CT | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-3413dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109248893 | ||||||
| chr8:109249033
|
TAG | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300-3554_1300-355 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249033 | ||||||
| chr8:109249088
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1300-3607A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249088 | ||||||
| chr8:109249218
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1300-3737A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249218 | ||||||
| chr8:109249378
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1300-3897G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249378 | ||||||
| chr8:109249395
|
G | A | 1 | a0003c0003t0004g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1300-3914C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249395 | ||||||
| chr8:109249430
|
A | T | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-3949T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249430 | ||||||
| chr8:109249460
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1300-3979C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249460 | ||||||
| chr8:109249574
|
T | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-4093A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249574 | ||||||
| chr8:109249654
|
C | T | 1 | a0004c0004t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1300-4173G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249654 | ||||||
| chr8:109249793
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1300-4312C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249793 | ||||||
| chr8:109249837
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1300-4356A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249837 | ||||||
| chr8:109249847
|
C | CT | 31 | a0001c0001t0001g0131a0002c0002t0002g0228a0002c0002t0002g0229others(28): Show | 32 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300-4367dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249847 | ||||||
| chr8:109249847
|
C | CTT | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1300-4368_1300-436 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249847 | ||||||
| chr8:109249847
|
C | CTTT | 6 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0126others(3): Show | 6 | HG01934.hp2 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-4369_1300-436 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249847 | ||||||
| chr8:109249973
|
G | A | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-4492C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109249973 | ||||||
| chr8:109250138
|
G | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1300-4657C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250138 | ||||||
| chr8:109250252
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1300-4771T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250252 | ||||||
| chr8:109250316
|
G | A | 2 | a0004c0004t0001g0062a0004c0004t0001g0141 | 2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1300-4835C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250316 | ||||||
| chr8:109250441
|
T | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300-4960A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250441 | ||||||
| chr8:109250487
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1300-5006A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250487 | ||||||
| chr8:109250506
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300-5025A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250506 | ||||||
| chr8:109250513
|
C | T | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1300-5032G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250513 | ||||||
| chr8:109250597
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1300-5116A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250597 | ||||||
| chr8:109250698
|
A | G | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1300-5217T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250698 | ||||||
| chr8:109250760
|
T | C | 40 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0205others(37): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1300-5279A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250760 | ||||||
| chr8:109250769
|
TTGA | T | 19 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(16): Show | 20 | HG01243.hp1 HG01934.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1300-5291_1300-528 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250769 | ||||||
| chr8:109250892
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1300-5411A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250892 | ||||||
| chr8:109250971
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1300-5490G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109250971 | ||||||
| chr8:109251083
|
C | G | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1300-5602G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251083 | ||||||
| chr8:109251168
|
CT | C | 11 | a0003c0003t0008g0030a0005c0005t0007g0171a0005c0005t0007g0172others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1300-5688delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251168 | ||||||
| chr8:109251176
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1300-5695A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251176 | ||||||
| chr8:109251181
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0123others(2): Show | 5 | NA18947.hp1 NA18992.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-5700A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251181 | ||||||
| chr8:109251182
|
C | CT | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1300-5702dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251182 | ||||||
| chr8:109251182
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0123others(3): Show | 6 | HG02738.hp1 NA18947.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-5701G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251182 | ||||||
| chr8:109251239
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-5758A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251239 | ||||||
| chr8:109251249
|
C | G | 7 | a0003c0003t0004g0213a0003c0003t0004g0214a0003c0003t0004g0215others(4): Show | 7 | HG01243.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-5768G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251249 | ||||||
| chr8:109251305
|
G | A | 2 | a0003c0003t0003g0176a0003c0003t0003g0177 | 2 | HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1300-5824C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251305 | ||||||
| chr8:109251330
|
G | T | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-5849C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251330 | ||||||
| chr8:109251362
|
G | A | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1300-5881C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251362 | ||||||
| chr8:109251647
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | NA18952.hp2 NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1300-6166A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251647 | ||||||
| chr8:109251653
|
CT | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-6173delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251653 | ||||||
| chr8:109251852
|
A | G | 1 | a0002c0002t0002g0269 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1300-6371T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251852 | ||||||
| chr8:109251853
|
C | G | 1 | a0002c0002t0002g0269 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1300-6372G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251853 | ||||||
| chr8:109251932
|
G | A | 2 | a0002c0002t0002g0256a0002c0002t0002g0279 | 2 | NA19072.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1300-6451C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109251932 | ||||||
| chr8:109252119
|
T | A | 1 | a0002c0002t0002g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1300-6638A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252119 | ||||||
| chr8:109252329
|
GCATAGAG others(139): Show |
G | 1 | a0005c0005t0007g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1300-6994_1300-684 others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252329 | ||||||
| chr8:109252350
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1300-6869C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252350 | ||||||
| chr8:109252397
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1300-6916G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252397 | ||||||
| chr8:109252452
|
T | TA | 8 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1300-6972dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252452 | ||||||
| chr8:109252468
|
A | G | 7 | a0002c0002t0002g0296a0002c0002t0002g0297a0002c0002t0002g0298others(4): Show | 7 | HG00597.hp1 HG00621.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-6987T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252468 | ||||||
| chr8:109252475
|
A | G | 2 | a0003c0003t0008g0032a0003c0003t0008g0033 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1300-6994T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252475 | ||||||
| chr8:109252573
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1300-7092C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252573 | ||||||
| chr8:109252644
|
T | C | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-7163A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252644 | ||||||
| chr8:109252802
|
G | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-7321C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252802 | ||||||
| chr8:109252936
|
T | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1300-7455A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252936 | ||||||
| chr8:109252947
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1300-7466C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109252947 | ||||||
| chr8:109253432
|
C | T | 1 | a0002c0002t0002g0279 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1300-7951G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253432 | ||||||
| chr8:109253621
|
C | CA | 3 | a0002c0002t0002g0319a0002c0002t0002g0320a0002c0002t0002g0321 | 3 | HG00558.hp1 HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1300-8141dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253621 | ||||||
| chr8:109253680
|
T | C | 1 | a0006c0006t0008g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1300-8199A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253680 | ||||||
| chr8:109253814
|
A | G | 3 | a0002c0002t0002g0235a0002c0002t0002g0236a0002c0002t0011g0010 | 4 | HG00438.hp1 HG00558.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-8333T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253814 | ||||||
| chr8:109253841
|
T | C | 38 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1300-8360A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253841 | ||||||
| chr8:109253850
|
G | GA | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-8370dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109253850 | ||||||
| chr8:109254096
|
T | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-8615A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109254096 | ||||||
| chr8:109254105
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1300-8624C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109254105 | ||||||
| chr8:109254203
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-8722T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109254203 | ||||||
| chr8:109254734
|
G | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-9253C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109254734 | ||||||
| chr8:109254858
|
G | C | 1 | a0002c0002t0002g0260 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1300-9377C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109254858 | ||||||
| chr8:109255077
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1300-9596T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255077 | ||||||
| chr8:109255145
|
C | G | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-9664G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255145 | ||||||
| chr8:109255274
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1300-9793T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255274 | ||||||
| chr8:109255674
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1300-10193G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255674 | ||||||
| chr8:109255678
|
GA | G | 31 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0091others(28): Show | 32 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1300-10198delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255678 | ||||||
| chr8:109255770
|
A | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300-10289T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255770 | ||||||
| chr8:109255818
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1300-10337G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255818 | ||||||
| chr8:109255875
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1300-10394G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255875 | ||||||
| chr8:109255924
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-10443A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255924 | ||||||
| chr8:109255965
|
T | C | 9 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | NA18947.hp1 NA18952.hp2 NA18992.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-10484A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255965 | ||||||
| chr8:109255968
|
GGAGGCTG others(130): Show |
G | 1 | a0003c0003t0003g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1300-10624_1300-10 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109255968 | ||||||
| chr8:109256086
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1300-10605G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256086 | ||||||
| chr8:109256127
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-10646C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256127 | ||||||
| chr8:109256161
|
T | C | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-10680A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256161 | ||||||
| chr8:109256192
|
C | T | 1 | a0002c0002t0002g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1300-10711G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256192 | ||||||
| chr8:109256252
|
A | T | 1 | a0004c0004t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1300-10771T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256252 | ||||||
| chr8:109256262
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1300-10781A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256262 | ||||||
| chr8:109256293
|
A | G | 1 | a0004c0004t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1300-10812T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256293 | ||||||
| chr8:109256311
|
C | A | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1300-10830G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256311 | ||||||
| chr8:109256460
|
C | CAATT | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1300-10980_1300-10 others(10): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256460 | ||||||
| chr8:109256518
|
G | T | 8 | a0003c0003t0006g0009a0003c0003t0006g0026a0003c0003t0006g0027others(5): Show | 9 | HG01109.hp1 HG01884.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1300-11037C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109256518 | ||||||
| chr8:109257002
|
T | C | 2 | a0002c0002t0002g0277a0002c0002t0002g0278 | 2 | NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1300-11521A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257002 | ||||||
| chr8:109257042
|
G | A | 3 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0174 | 3 | HG02145.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1300-11561C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257042 | ||||||
| chr8:109257248
|
T | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1300-11767A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257248 | ||||||
| chr8:109257377
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1300-11896A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257377 | ||||||
| chr8:109257386
|
C | G | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-11905G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257386 | ||||||
| chr8:109257636
|
A | G | 2 | a0003c0003t0003g0034a0003c0003t0003g0038 | 2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1300-12155T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257636 | ||||||
| chr8:109257820
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1300-12339T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257820 | ||||||
| chr8:109257964
|
T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1300-12483A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109257964 | ||||||
| chr8:109258302
|
G | A | 8 | a0003c0003t0004g0015a0003c0003t0004g0338a0003c0003t0004g0339others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+12703C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258302 | ||||||
| chr8:109258466
|
C | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+12539G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258466 | ||||||
| chr8:109258546
|
C | A | 1 | a0004c0004t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1299+12459G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258546 | ||||||
| chr8:109258562
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1299+12443A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258562 | ||||||
| chr8:109258871
|
T | C | 2 | a0002c0002t0002g0308a0002c0002t0002g0309 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1299+12134A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258871 | ||||||
| chr8:109258947
|
C | T | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+12058G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109258947 | ||||||
| chr8:109259090
|
A | G | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1299+11915T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259090 | ||||||
| chr8:109259262
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+11743T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259262 | ||||||
| chr8:109259324
|
T | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+11681A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259324 | ||||||
| chr8:109259415
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1299+11590C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259415 | ||||||
| chr8:109259468
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1299+11537T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259468 | ||||||
| chr8:109259505
|
G | A | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+11500C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259505 | ||||||
| chr8:109259511
|
T | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1299+11494A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109259511 | ||||||
| chr8:109260234
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+10771A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260234 | ||||||
| chr8:109260320
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+10685C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260320 | ||||||
| chr8:109260369
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1299+10636C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260369 | ||||||
| chr8:109260461
|
A | G | 1 | a0003c0003t0003g0169 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1299+10544T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260461 | ||||||
| chr8:109260476
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1299+10529G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260476 | ||||||
| chr8:109260511
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1299+10494G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260511 | ||||||
| chr8:109260558
|
T | G | 38 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1299+10447A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260558 | ||||||
| chr8:109260591
|
G | A | 1 | a0004c0004t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1299+10414C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260591 | ||||||
| chr8:109260680
|
G | A | 9 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | NA18947.hp1 NA18952.hp2 NA18992.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+10325C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260680 | ||||||
| chr8:109260697
|
C | T | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1299+10308G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260697 | ||||||
| chr8:109260725
|
T | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1299+10280A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260725 | ||||||
| chr8:109260765
|
C | CATCTCTG others(2): Show |
5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+10231_1299+10 others(15): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260765 | ||||||
| chr8:109260810
|
T | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+10195A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260810 | ||||||
| chr8:109260900
|
A | G | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+10105T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260900 | ||||||
| chr8:109260963
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+10042A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260963 | ||||||
| chr8:109260966
|
A | G | 1 | a0002c0002t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1299+10039T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260966 | ||||||
| chr8:109260994
|
G | A | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1299+10011C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109260994 | ||||||
| chr8:109261164
|
T | C | 1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1299+9841A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261164 | ||||||
| chr8:109261400
|
C | T | 1 | a0002c0002t0002g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1299+9605G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261400 | ||||||
| chr8:109261562
|
T | C | 1 | a0002c0002t0002g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1299+9443A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261562 | ||||||
| chr8:109261623
|
AAAAAGGC others(1): Show |
A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+9374_1299+938 others(12): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261623 | ||||||
| chr8:109261631
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1299+9374C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261631 | ||||||
| chr8:109261890
|
A | G | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1299+9115T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261890 | ||||||
| chr8:109261895
|
C | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0052others(11): Show | 16 | HG00735.hp2 HG01081.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1299+9110G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261895 | ||||||
| chr8:109261997
|
G | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+9008C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109261997 | ||||||
| chr8:109262018
|
C | CA | 8 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0124others(5): Show | 8 | HG02027.hp2 HG03471.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1299+8986dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262018 | ||||||
| chr8:109262055
|
C | T | 2 | a0002c0002t0002g0243a0002c0002t0002g0282 | 2 | HG01123.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1299+8950G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262055 | ||||||
| chr8:109262256
|
C | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+8749G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262256 | ||||||
| chr8:109262286
|
G | A | 1 | a0003c0003t0003g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1299+8719C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262286 | ||||||
| chr8:109262443
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+8562T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262443 | ||||||
| chr8:109262656
|
T | C | 1 | a0004c0004t0001g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1299+8349A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262656 | ||||||
| chr8:109262684
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1299+8321A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262684 | ||||||
| chr8:109262794
|
G | A | 1 | a0002c0002t0002g0319 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1299+8211C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262794 | ||||||
| chr8:109262820
|
C | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+8185G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262820 | ||||||
| chr8:109262848
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0118 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1299+8157C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262848 | ||||||
| chr8:109262969
|
C | T | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1299+8036G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109262969 | ||||||
| chr8:109263030
|
G | A | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1299+7975C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263030 | ||||||
| chr8:109263054
|
C | CA | 54 | a0002c0002t0002g0012a0002c0002t0002g0233a0002c0002t0002g0235others(51): Show | 56 | HG00438.hp1 HG00597.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1299+7950dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAA | 32 | a0002c0002t0002g0262a0002c0002t0002g0299a0003c0003t0003g0036others(29): Show | 33 | HG00621.hp1 HG00639.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1299+7949_1299+795 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAA | 21 | a0001c0001t0001g0342a0003c0003t0003g0176a0003c0003t0003g0177others(18): Show | 22 | HG00741.hp2 HG01123.hp1 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.1299+7948_1299+795 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAA | 7 | a0003c0003t0003g0199a0003c0003t0005g0018a0003c0003t0005g0019others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+7947_1299+795 others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0052others(25): Show | 30 | HG00140.hp2 HG00280.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+7945_1299+795 others(10): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAAA | 44 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0058others(41): Show | 47 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.1299+7944_1299+795 others(11): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAAA others(1): Show |
43 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(40): Show | 44 | HG00140.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1299+7943_1299+795 others(12): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0063others(20): Show | 24 | HG01891.hp1 HG02027.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1299+7942_1299+795 others(13): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0095 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1299+7941_1299+795 others(14): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0132 | 2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1299+7940_1299+795 others(15): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263054
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0002g0297 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1299+7941_1299+795 others(14): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263054 | ||||||
| chr8:109263070
|
A | C | 1 | a0004c0004t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1299+7935T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263070 | ||||||
| chr8:109263200
|
C | A | 3 | a0002c0002t0002g0296a0002c0002t0002g0297a0002c0002t0002g0316 | 3 | NA18952.hp1 NA18954.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1299+7805G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263200 | ||||||
| chr8:109263257
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+7748A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263257 | ||||||
| chr8:109263339
|
T | A | 1 | a0002c0002t0002g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1299+7666A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263339 | ||||||
| chr8:109263405
|
T | C | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+7600A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263405 | ||||||
| chr8:109263517
|
G | A | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1299+7488C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263517 | ||||||
| chr8:109263582
|
A | G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1299+7423T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263582 | ||||||
| chr8:109263602
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+7403G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263602 | ||||||
| chr8:109263625
|
C | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+7380G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263625 | ||||||
| chr8:109263752
|
G | A | 1 | a0002c0002t0002g0264 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1299+7253C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263752 | ||||||
| chr8:109263757
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+7248A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263757 | ||||||
| chr8:109263944
|
C | T | 2 | a0003c0003t0004g0219a0003c0003t0004g0341 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1299+7061G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109263944 | ||||||
| chr8:109264061
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1299+6944A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264061 | ||||||
| chr8:109264100
|
T | C | 1 | a0002c0002t0002g0298 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1299+6905A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264100 | ||||||
| chr8:109264133
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+6872G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264133 | ||||||
| chr8:109264280
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1299+6725C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264280 | ||||||
| chr8:109264390
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+6615A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264390 | ||||||
| chr8:109264719
|
G | T | 1 | a0002c0002t0002g0235 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1299+6286C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264719 | ||||||
| chr8:109264851
|
C | T | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299+6154G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264851 | ||||||
| chr8:109264876
|
G | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1299+6129C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109264876 | ||||||
| chr8:109265068
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1299+5937C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265068 | ||||||
| chr8:109265326
|
A | AG | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+5678dupC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265326 | ||||||
| chr8:109265352
|
T | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+5653A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265352 | ||||||
| chr8:109265358
|
G | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+5647C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265358 | ||||||
| chr8:109265414
|
T | C | 1 | a0005c0005t0007g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+5591A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265414 | ||||||
| chr8:109265511
|
T | G | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+5494A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265511 | ||||||
| chr8:109265546
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02451.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1299+5459C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265546 | ||||||
| chr8:109265798
|
A | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+5207T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265798 | ||||||
| chr8:109265843
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+5162C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265843 | ||||||
| chr8:109265935
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+5070G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109265935 | ||||||
| chr8:109266132
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1299+4873T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266132 | ||||||
| chr8:109266157
|
C | CAT | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1299+4846_1299+484 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266157 | ||||||
| chr8:109266232
|
AT | A | 67 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(64): Show | 69 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1299+4772delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266232 | ||||||
| chr8:109266236
|
T | G | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1299+4769A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266236 | ||||||
| chr8:109266289
|
G | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | NA18966.hp1 NA19001.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+4716C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266289 | ||||||
| chr8:109266386
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+4619G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266386 | ||||||
| chr8:109266392
|
A | AT | 18 | a0002c0002t0002g0012a0002c0002t0002g0205a0002c0002t0002g0228others(15): Show | 19 | HG00735.hp1 HG01175.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1299+4612dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266392
|
A | ATT | 27 | a0003c0003t0003g0034a0003c0003t0003g0038a0003c0003t0003g0039others(24): Show | 27 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1299+4611_1299+461 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266392
|
A | ATTT | 9 | a0002c0002t0002g0321a0003c0003t0003g0035a0003c0003t0003g0036others(6): Show | 9 | HG02135.hp2 HG02615.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+4610_1299+461 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266392
|
AT | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0079others(32): Show | 37 | HG00621.hp2 HG00735.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1299+4612delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266392
|
ATT | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1299+4611_1299+461 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266392
|
ATTT | A | 18 | a0001c0001t0001g0089a0001c0001t0001g0224a0001c0001t0019g0084others(15): Show | 18 | HG01109.hp1 HG01934.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1299+4610_1299+461 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266392 | ||||||
| chr8:109266461
|
G | A | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+4544C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266461 | ||||||
| chr8:109266465
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1299+4540G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266465 | ||||||
| chr8:109266469
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1299+4536A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266469 | ||||||
| chr8:109266486
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1299+4519G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266486 | ||||||
| chr8:109266523
|
T | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1299+4482A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266523 | ||||||
| chr8:109266535
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+4470G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266535 | ||||||
| chr8:109266715
|
T | C | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299+4290A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266715 | ||||||
| chr8:109266750
|
C | T | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+4255G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266750 | ||||||
| chr8:109266789
|
A | G | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+4216T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109266789 | ||||||
| chr8:109267025
|
T | C | 1 | a0003c0003t0003g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1299+3980A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267025 | ||||||
| chr8:109267120
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1299+3885G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267120 | ||||||
| chr8:109267126
|
T | C | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1299+3879A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267126 | ||||||
| chr8:109267445
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1299+3560T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267445 | ||||||
| chr8:109267517
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1299+3488C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267517 | ||||||
| chr8:109267715
|
A | G | 1 | a0003c0003t0004g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1299+3290T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267715 | ||||||
| chr8:109267817
|
C | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+3188G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109267817 | ||||||
| chr8:109268027
|
C | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+2978G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268027 | ||||||
| chr8:109268202
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1299+2803T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268202 | ||||||
| chr8:109268244
|
A | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+2761T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268244 | ||||||
| chr8:109268291
|
C | G | 3 | a0002c0002t0002g0228a0002c0002t0002g0229a0002c0002t0016g0230 | 3 | HG00735.hp1 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1299+2714G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268291 | ||||||
| chr8:109268416
|
C | T | 2 | a0003c0003t0004g0219a0003c0003t0004g0341 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1299+2589G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268416 | ||||||
| chr8:109268440
|
A | T | 1 | a0002c0002t0002g0307 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1299+2565T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268440 | ||||||
| chr8:109268559
|
T | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+2446A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268559 | ||||||
| chr8:109268624
|
G | A | 4 | a0002c0002t0002g0251a0002c0002t0002g0252a0002c0002t0002g0313others(1): Show | 4 | NA18949.hp1 NA18983.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+2381C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268624 | ||||||
| chr8:109268637
|
T | C | 3 | a0003c0003t0006g0009a0003c0003t0006g0212a0003c0003t0006g0343 | 4 | HG01884.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1299+2368A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268637 | ||||||
| chr8:109268700
|
G | A | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1299+2305C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268700 | ||||||
| chr8:109268781
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1299+2224G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268781 | ||||||
| chr8:109268833
|
G | C | 5 | a0003c0003t0003g0178a0003c0003t0003g0179a0003c0003t0003g0180others(2): Show | 5 | NA18970.hp2 NA18981.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+2172C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268833 | ||||||
| chr8:109268838
|
G | A | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+2167C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268838 | ||||||
| chr8:109268918
|
T | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+2087A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109268918 | ||||||
| chr8:109269052
|
T | C | 1 | a0001c0001t0001g0332 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1299+1953A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269052 | ||||||
| chr8:109269251
|
T | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1299+1754A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269251 | ||||||
| chr8:109269453
|
G | C | 32 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(29): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1299+1552C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269453 | ||||||
| chr8:109269558
|
C | T | 1 | a0004c0004t0001g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1299+1447G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269558 | ||||||
| chr8:109269559
|
G | A | 1 | a0002c0002t0002g0319 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1299+1446C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269559 | ||||||
| chr8:109269604
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1299+1401C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269604 | ||||||
| chr8:109269945
|
TA | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1299+1059delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269945 | ||||||
| chr8:109269945
|
TAA | T | 13 | a0003c0003t0003g0180a0003c0003t0005g0001a0003c0003t0005g0017others(10): Show | 14 | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1299+1058_1299+105 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269945 | ||||||
| chr8:109269980
|
C | A | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1299+1025G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109269980 | ||||||
| chr8:109270027
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1299+978G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270027 | ||||||
| chr8:109270061
|
CGGGGGCG others(10): Show |
C | 1 | a0003c0003t0004g0338 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1299+927_1299+943d others(19): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270061 | ||||||
| chr8:109270067
|
C | G | 1 | a0002c0002t0002g0248 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1299+938G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270067
|
C | T | 2 | a0003c0003t0004g0015a0003c0003t0004g0340 | 3 | HG02970.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1299+938G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270067
|
CG | C | 83 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(80): Show | 87 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1299+937delC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270067
|
CGG | C | 30 | a0002c0002t0002g0240a0002c0002t0002g0246a0002c0002t0002g0247others(27): Show | 31 | HG01071.hp2 HG01167.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1299+936_1299+937d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270067
|
CGGGGG | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0064others(26): Show | 30 | HG00423.hp1 HG01074.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+933_1299+937d others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270067
|
CGGGGGG | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1299+932_1299+937d others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | ||||||
| chr8:109270068
|
G | T | 1 | a0003c0003t0004g0344 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1299+937C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270068 | ||||||
| chr8:109270069
|
G | T | 1 | a0003c0003t0004g0339 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1299+936C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270069 | ||||||
| chr8:109270073
|
G | T | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1299+932C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270073 | ||||||
| chr8:109270083
|
T | G | 2 | a0003c0003t0003g0179a0003c0003t0003g0181 | 2 | NA18981.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1299+922A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270083 | ||||||
| chr8:109270085
|
C | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1299+920G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270085 | ||||||
| chr8:109270088
|
T | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(340): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1299+917A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270088 | ||||||
| chr8:109270089
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1299+916T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270089 | ||||||
| chr8:109270089
|
A | T | 2 | a0003c0003t0003g0179a0003c0003t0003g0181 | 2 | NA18981.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1299+916T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270089 | ||||||
| chr8:109270090
|
A | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(340): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1299+915T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270090 | ||||||
| chr8:109270092
|
G | C | 3 | a0003c0003t0003g0179a0003c0003t0003g0181a0003c0003t0003g0206 | 3 | NA18981.hp1 NA18985.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1299+913C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270092 | ||||||
| chr8:109270155
|
G | A | 1 | a0003c0003t0006g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1299+850C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270155 | ||||||
| chr8:109270218
|
G | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+787C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270218 | ||||||
| chr8:109270721
|
GA | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+283delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270721 | ||||||
| chr8:109270733
|
G | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1299+272C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270733 | ||||||
| chr8:109270735
|
G | A | 3 | a0002c0002t0002g0277a0002c0002t0002g0278a0002c0002t0002g0314 | 3 | NA18966.hp2 NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1299+270C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270735 | ||||||
| chr8:109270809
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1299+196T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270809 | ||||||
| chr8:109271158
|
T | G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1174-28A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271158 | ||||||
| chr8:109271425
|
C | T | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-295G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271425 | ||||||
| chr8:109271494
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1174-364G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271494 | ||||||
| chr8:109271495
|
G | C | 1 | a0003c0003t0006g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1174-365C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271495 | ||||||
| chr8:109271542
|
A | C | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1174-412T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271542 | ||||||
| chr8:109271564
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1174-434T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271564 | ||||||
| chr8:109271656
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | NA18952.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1174-526G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271656 | ||||||
| chr8:109271946
|
A | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-816T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109271946 | ||||||
| chr8:109272129
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1174-999T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272129 | ||||||
| chr8:109272143
|
A | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | NA18747.hp1 NA18998.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-1013T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272143 | ||||||
| chr8:109272158
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-1028G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272158 | ||||||
| chr8:109272196
|
G | C | 1 | a0002c0002t0002g0248 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1174-1066C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272196 | ||||||
| chr8:109272255
|
CAAT | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-1128_1174-112 others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272255 | ||||||
| chr8:109272364
|
A | AAC | 40 | a0002c0002t0002g0228a0002c0002t0002g0229a0002c0002t0002g0243others(37): Show | 41 | HG00735.hp1 HG00741.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1174-1236_1174-123 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272364 | ||||||
| chr8:109272364
|
A | AACAC | 5 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1238_1174-123 others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272364 | ||||||
| chr8:109272364
|
AAC | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1174-1236_1174-123 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272364 | ||||||
| chr8:109272364
|
AACACACA others(1): Show |
A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-1242_1174-123 others(12): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272364 | ||||||
| chr8:109272414
|
T | C | 10 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(7): Show | 10 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-1284A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272414 | ||||||
| chr8:109272467
|
T | A | 5 | a0002c0002t0002g0205a0002c0002t0002g0210a0002c0002t0002g0234others(2): Show | 5 | HG02083.hp1 HG03927.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-1337A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272467 | ||||||
| chr8:109272658
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-1528C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272658 | ||||||
| chr8:109272864
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1174-1734G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272864 | ||||||
| chr8:109272919
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-1789A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272919 | ||||||
| chr8:109272943
|
G | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-1813C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109272943 | ||||||
| chr8:109273038
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-1908G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273038 | ||||||
| chr8:109273084
|
G | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-1954C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273084 | ||||||
| chr8:109273099
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1174-1969G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273099 | ||||||
| chr8:109273208
|
AGT | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1174-2080_1174-207 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273208 | ||||||
| chr8:109273356
|
C | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1173+1996G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273356 | ||||||
| chr8:109273429
|
A | G | 32 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(29): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1173+1923T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273429 | ||||||
| chr8:109273439
|
A | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1173+1913T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273439 | ||||||
| chr8:109273503
|
T | C | 3 | a0001c0001t0001g0016a0002c0002t0002g0322a0002c0002t0002g0323 | 3 | NA18522.hp2 NA18970.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1173+1849A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273503 | ||||||
| chr8:109273530
|
G | A | 2 | a0003c0003t0003g0176a0003c0003t0003g0177 | 2 | HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1173+1822C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273530 | ||||||
| chr8:109273541
|
G | C | 1 | a0003c0003t0004g0337 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1173+1811C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273541 | ||||||
| chr8:109273629
|
T | C | 6 | a0005c0005t0007g0173a0005c0005t0007g0201a0005c0005t0007g0202others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1723A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273629 | ||||||
| chr8:109273922
|
A | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+1430T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109273922 | ||||||
| chr8:109274108
|
G | T | 2 | a0003c0003t0004g0219a0003c0003t0004g0341 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1173+1244C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274108 | ||||||
| chr8:109274301
|
T | C | 1 | a0004c0004t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1173+1051A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274301 | ||||||
| chr8:109274460
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1173+892C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274460 | ||||||
| chr8:109274763
|
CATT | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+586_1173+588d others(5): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274763 | ||||||
| chr8:109274777
|
G | A | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+575C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274777 | ||||||
| chr8:109274847
|
G | C | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1173+505C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274847 | ||||||
| chr8:109274909
|
G | T | 1 | a0002c0002t0002g0272 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1173+443C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274909 | ||||||
| chr8:109274944
|
T | C | 1 | a0002c0002t0002g0326 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1173+408A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109274944 | ||||||
| chr8:109275113
|
TAA | T | 9 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(6): Show | 9 | HG01261.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+237_1173+238d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109275113 | ||||||
| chr8:109275325
|
A | G | 1 | a0006c0006t0008g0334 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1173+27T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109275325 | ||||||
| chr8:109275328
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1173+24G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 7/9 | chr8 | 109275328 | ||||||
| chr8:109275509
|
A | G | 1 | a0003c0011t0008g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1029-13T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109275509 | ||||||
| chr8:109275522
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-26A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109275522 | ||||||
| chr8:109275603
|
G | T | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1029-107C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109275603 | ||||||
| chr8:109276068
|
C | T | 4 | a0002c0002t0002g0304a0002c0002t0002g0305a0002c0002t0002g0306others(1): Show | 4 | HG01175.hp1 HG01256.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029-572G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276068 | ||||||
| chr8:109276262
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-766C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276262 | ||||||
| chr8:109276263
|
A | AAGTAACC others(11): Show |
1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-768_1029-767i others(20): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276263 | ||||||
| chr8:109276282
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-786G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276282 | ||||||
| chr8:109276284
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-788A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276284 | ||||||
| chr8:109276285
|
C | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-789G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276285 | ||||||
| chr8:109276295
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-799T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276295 | ||||||
| chr8:109276307
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-811T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276307 | ||||||
| chr8:109276312
|
G | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-816C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276312 | ||||||
| chr8:109276318
|
T | G | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-822A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276318 | ||||||
| chr8:109276324
|
G | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-828C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276324 | ||||||
| chr8:109276443
|
T | G | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-947A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276443 | ||||||
| chr8:109276444
|
G | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-948C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276444 | ||||||
| chr8:109276445
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-949G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276445 | ||||||
| chr8:109276446
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-950T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276446 | ||||||
| chr8:109276457
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-961T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276457 | ||||||
| chr8:109276461
|
A | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-965T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276461 | ||||||
| chr8:109276462
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-966G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276462 | ||||||
| chr8:109276499
|
G | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1003C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276499 | ||||||
| chr8:109276510
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1014A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276510 | ||||||
| chr8:109276528
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1032G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276528 | ||||||
| chr8:109276536
|
T | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-1040A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276536 | ||||||
| chr8:109276548
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1052A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276548 | ||||||
| chr8:109276551
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1055T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276551 | ||||||
| chr8:109276595
|
A | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1099T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276595 | ||||||
| chr8:109276660
|
A | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1029-1164T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276660 | ||||||
| chr8:109276675
|
G | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1179C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276675 | ||||||
| chr8:109276681
|
G | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1185C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276681 | ||||||
| chr8:109276682
|
A | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1186T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276682 | ||||||
| chr8:109276687
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1191G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276687 | ||||||
| chr8:109276688
|
A | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1192T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276688 | ||||||
| chr8:109276693
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1197G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276693 | ||||||
| chr8:109276765
|
C | G | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1269G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276765 | ||||||
| chr8:109276766
|
G | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1270C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276766 | ||||||
| chr8:109276808
|
G | A | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1029-1312C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276808 | ||||||
| chr8:109276854
|
G | A | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1029-1358C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276854 | ||||||
| chr8:109276874
|
G | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1378C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276874 | ||||||
| chr8:109276887
|
T | A | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1391A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276887 | ||||||
| chr8:109276889
|
C | T | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1393G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276889 | ||||||
| chr8:109276890
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1394A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276890 | ||||||
| chr8:109276891
|
G | C | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1395C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276891 | ||||||
| chr8:109276893
|
C | G | 1 | a0002c0002t0002g0288 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1029-1397G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276893 | ||||||
| chr8:109276938
|
T | C | 1 | a0002c0002t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1029-1442A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276938 | ||||||
| chr8:109276953
|
G | A | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1029-1457C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276953 | ||||||
| chr8:109276960
|
G | A | 1 | a0002c0002t0002g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1029-1464C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276960 | ||||||
| chr8:109276968
|
A | G | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1029-1472T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109276968 | ||||||
| chr8:109277087
|
A | G | 4 | a0002c0002t0002g0233a0002c0002t0002g0293a0002c0002t0002g0294others(1): Show | 4 | NA18971.hp2 NA19009.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-1591T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277087 | ||||||
| chr8:109277304
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1029-1808T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277304 | ||||||
| chr8:109277352
|
C | T | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1029-1856G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277352 | ||||||
| chr8:109277409
|
C | T | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1029-1913G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277409 | ||||||
| chr8:109277464
|
C | CA | 33 | a0002c0002t0002g0237a0003c0003t0004g0015a0003c0003t0004g0041others(30): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1029-1969dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277464 | ||||||
| chr8:109277552
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1029-2056T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277552 | ||||||
| chr8:109277626
|
A | G | 1 | a0003c0003t0004g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1029-2130T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277626 | ||||||
| chr8:109277636
|
T | C | 1 | a0003c0003t0004g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1029-2140A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277636 | ||||||
| chr8:109277785
|
T | C | 9 | a0003c0003t0003g0170a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029-2289A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277785 | ||||||
| chr8:109277807
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1029-2311G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109277807 | ||||||
| chr8:109278014
|
G | C | 4 | a0002c0002t0002g0245a0002c0002t0002g0246a0002c0002t0002g0247others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-2518C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278014 | ||||||
| chr8:109278190
|
A | G | 1 | a0002c0002t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1029-2694T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278190 | ||||||
| chr8:109278391
|
T | A | 6 | a0005c0005t0007g0173a0005c0005t0007g0201a0005c0005t0007g0202others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028+2577A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278391 | ||||||
| chr8:109278524
|
C | T | 1 | a0002c0002t0015g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1028+2444G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278524 | ||||||
| chr8:109278529
|
T | C | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1028+2439A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278529 | ||||||
| chr8:109278535
|
C | A | 5 | a0003c0003t0004g0213a0003c0003t0004g0214a0003c0003t0004g0215others(2): Show | 5 | HG01243.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1028+2433G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278535 | ||||||
| chr8:109278588
|
T | G | 32 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(29): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1028+2380A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278588 | ||||||
| chr8:109278594
|
G | C | 1 | a0003c0003t0003g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1028+2374C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278594 | ||||||
| chr8:109278776
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01099.hp2 HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1028+2192T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278776 | ||||||
| chr8:109278928
|
T | C | 2 | a0002c0002t0002g0249a0002c0002t0002g0250 | 2 | HG00597.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1028+2040A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109278928 | ||||||
| chr8:109279001
|
A | G | 5 | a0002c0002t0008g0333a0006c0006t0008g0168a0006c0006t0008g0334others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+1967T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279001 | ||||||
| chr8:109279165
|
G | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1028+1803C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279165 | ||||||
| chr8:109279232
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1028+1736A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279232 | ||||||
| chr8:109279281
|
T | C | 1 | a0001c0001t0018g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1028+1687A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279281 | ||||||
| chr8:109279496
|
TG | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1028+1471delC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279496 | ||||||
| chr8:109279628
|
A | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028+1340T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279628 | ||||||
| chr8:109279646
|
T | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028+1322A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279646 | ||||||
| chr8:109279676
|
T | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028+1292A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279676 | ||||||
| chr8:109279681
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0052others(11): Show | 16 | HG00735.hp2 HG01081.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1028+1287T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279681 | ||||||
| chr8:109279697
|
G | T | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1028+1271C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279697 | ||||||
| chr8:109279978
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1028+990T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109279978 | ||||||
| chr8:109280056
|
A | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028+912T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280056 | ||||||
| chr8:109280149
|
GATTA | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028+815_1028+818d others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280149 | ||||||
| chr8:109280155
|
T | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1028+813A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280155 | ||||||
| chr8:109280171
|
T | C | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1028+797A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280171 | ||||||
| chr8:109280296
|
T | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028+672A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280296 | ||||||
| chr8:109280387
|
A | G | 32 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(29): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1028+581T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280387 | ||||||
| chr8:109280447
|
G | A | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1028+521C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280447 | ||||||
| chr8:109280451
|
A | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028+517T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280451 | ||||||
| chr8:109280565
|
GGAGGCA | G | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1028+397_1028+402d others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280565 | ||||||
| chr8:109280955
|
TA | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1028+12delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280955 | ||||||
| chr8:109280957
|
A | T | 5 | a0003c0003t0004g0213a0003c0003t0004g0214a0003c0003t0004g0215others(2): Show | 5 | HG01243.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1028+11T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 6/9 | chr8 | 109280957 | ||||||
| chr8:109281179
|
G | C | 1 | a0002c0002t0002g0310 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.824-7C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281179 | ||||||
| chr8:109281202
|
A | AT | 4 | a0002c0002t0002g0304a0002c0002t0002g0305a0002c0002t0002g0306others(1): Show | 4 | HG01175.hp1 HG01256.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-31dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281202 | ||||||
| chr8:109281369
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-197G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281369 | ||||||
| chr8:109281409
|
A | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-237T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281409 | ||||||
| chr8:109281472
|
T | C | 1 | a0003c0003t0003g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.824-300A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281472 | ||||||
| chr8:109281967
|
C | A | 1 | a0003c0003t0003g0189 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.824-795G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109281967 | ||||||
| chr8:109282177
|
C | G | 1 | a0002c0002t0002g0310 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.824-1005G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282177 | ||||||
| chr8:109282217
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.824-1045G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282217 | ||||||
| chr8:109282222
|
C | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.824-1050G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282222 | ||||||
| chr8:109282320
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-1148G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282320 | ||||||
| chr8:109282329
|
T | A | 1 | a0003c0003t0003g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.824-1157A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282329 | ||||||
| chr8:109282466
|
AAAAC | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-1298_824-1295d others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282466 | ||||||
| chr8:109282643
|
T | C | 3 | a0002c0002t0002g0296a0002c0002t0002g0297a0002c0002t0002g0316 | 3 | NA18952.hp1 NA18954.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.824-1471A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282643 | ||||||
| chr8:109282681
|
G | A | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.824-1509C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282681 | ||||||
| chr8:109282683
|
G | T | 1 | a0002c0002t0002g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.824-1511C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282683 | ||||||
| chr8:109282686
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.824-1514C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282686 | ||||||
| chr8:109282751
|
C | T | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-1579G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282751 | ||||||
| chr8:109282796
|
C | T | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.824-1624G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282796 | ||||||
| chr8:109282830
|
A | G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.824-1658T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282830 | ||||||
| chr8:109282833
|
A | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1661T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282833 | ||||||
| chr8:109282843
|
C | CA | 41 | a0001c0001t0001g0111a0003c0003t0003g0169a0003c0003t0003g0194others(38): Show | 43 | HG01109.hp1 HG01167.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.824-1672dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282843 | ||||||
| chr8:109282843
|
CA | C | 9 | a0001c0001t0001g0077a0002c0002t0002g0318a0003c0003t0003g0206others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-1672delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282843 | ||||||
| chr8:109282882
|
TA | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1711delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282882 | ||||||
| chr8:109282903
|
G | C | 1 | a0003c0003t0004g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.824-1731C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282903 | ||||||
| chr8:109282958
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-1786T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282958 | ||||||
| chr8:109282982
|
TCAAAGCA others(7): Show |
T | 2 | a0002c0002t0002g0271a0002c0002t0002g0280 | 2 | NA18985.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.824-1824_824-1811d others(16): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109282982 | ||||||
| chr8:109283106
|
C | T | 1 | a0002c0002t0002g0318 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.824-1934G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283106 | ||||||
| chr8:109283139
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.824-1967T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283139 | ||||||
| chr8:109283319
|
T | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.824-2147A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283319 | ||||||
| chr8:109283341
|
GA | G | 5 | a0002c0002t0002g0277a0002c0002t0002g0278a0002c0002t0002g0284others(2): Show | 5 | HG02040.hp1 HG02135.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2170delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283341 | ||||||
| chr8:109283386
|
A | G | 3 | a0003c0003t0003g0169a0003c0003t0003g0194a0003c0003t0003g0196 | 3 | HG01167.hp2 HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.824-2214T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283386 | ||||||
| chr8:109283472
|
A | T | 1 | a0003c0003t0003g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-2300T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283472 | ||||||
| chr8:109283535
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.824-2363T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283535 | ||||||
| chr8:109283675
|
CTA | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.824-2505_824-2504d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283675 | ||||||
| chr8:109283708
|
C | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.824-2536G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283708 | ||||||
| chr8:109283884
|
C | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-2712G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283884 | ||||||
| chr8:109283989
|
T | TA | 9 | a0002c0002t0002g0312a0003c0003t0003g0176a0003c0003t0003g0179others(6): Show | 9 | HG01109.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-2818dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283989 | ||||||
| chr8:109283989
|
TA | T | 14 | a0002c0002t0002g0257a0002c0002t0002g0259a0002c0002t0008g0333others(11): Show | 14 | HG01074.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-2818delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283989 | ||||||
| chr8:109283989
|
TAAA | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.824-2820_824-2818d others(5): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283989 | ||||||
| chr8:109283998
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.824-2826T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109283998 | ||||||
| chr8:109284003
|
A | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.824-2831T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284003 | ||||||
| chr8:109284006
|
AAC | A | 10 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(7): Show | 11 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-2836_824-2835d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284006 | ||||||
| chr8:109284007
|
AC | A | 4 | a0003c0003t0003g0169a0003c0003t0003g0178a0003c0003t0003g0180others(1): Show | 4 | HG01167.hp2 HG02818.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-2836delG | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284007 | ||||||
| chr8:109284008
|
C | A | 28 | a0003c0003t0003g0170a0003c0003t0003g0175a0003c0003t0003g0176others(25): Show | 28 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.824-2836G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284008 | ||||||
| chr8:109284122
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.824-2950C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284122 | ||||||
| chr8:109284162
|
A | G | 1 | a0002c0002t0002g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.824-2990T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284162 | ||||||
| chr8:109284219
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG01069.hp2 HG01071.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-3047G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284219 | ||||||
| chr8:109284763
|
G | GA | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0123others(2): Show | 5 | NA18947.hp1 NA18992.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-3592dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284763 | ||||||
| chr8:109284957
|
A | G | 1 | a0003c0003t0006g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824-3785T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109284957 | ||||||
| chr8:109285006
|
CA | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.824-3835delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285006 | ||||||
| chr8:109285076
|
A | G | 2 | a0003c0003t0003g0034a0003c0003t0003g0038 | 2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.824-3904T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285076 | ||||||
| chr8:109285104
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.824-3932G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285104 | ||||||
| chr8:109285205
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-4033A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285205 | ||||||
| chr8:109285246
|
C | CG | 10 | a0001c0001t0001g0049a0001c0001t0001g0155a0002c0002t0002g0245others(7): Show | 10 | HG01099.hp2 HG01952.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.824-4075dupC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285246 | ||||||
| chr8:109285257
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.824-4085G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285257 | ||||||
| chr8:109285282
|
GAGA | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.824-4113_824-4111d others(5): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285282 | ||||||
| chr8:109285538
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.823+4213T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285538 | ||||||
| chr8:109285579
|
A | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+4172T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285579 | ||||||
| chr8:109285739
|
G | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.823+4012C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285739 | ||||||
| chr8:109285816
|
T | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.823+3935A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285816 | ||||||
| chr8:109285826
|
G | T | 38 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.823+3925C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109285826 | ||||||
| chr8:109286337
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.823+3414T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109286337 | ||||||
| chr8:109286482
|
T | C | 1 | a0003c0003t0003g0169 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.823+3269A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109286482 | ||||||
| chr8:109286601
|
C | G | 1 | a0002c0002t0015g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+3150G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109286601 | ||||||
| chr8:109286828
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.823+2923T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109286828 | ||||||
| chr8:109287082
|
G | A | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+2669C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287082 | ||||||
| chr8:109287113
|
T | C | 1 | a0002c0002t0002g0257 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.823+2638A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287113 | ||||||
| chr8:109287194
|
T | A | 3 | a0002c0002t0002g0293a0002c0002t0002g0294a0002c0002t0002g0295 | 3 | NA19009.hp1 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.823+2557A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287194 | ||||||
| chr8:109287289
|
T | C | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.823+2462A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287289 | ||||||
| chr8:109287456
|
C | G | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0144others(3): Show | 6 | HG00735.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+2295G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287456 | ||||||
| chr8:109287531
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.823+2220A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287531 | ||||||
| chr8:109287593
|
A | C | 2 | a0002c0002t0002g0304a0002c0002t0002g0305 | 2 | HG01261.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.823+2158T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287593 | ||||||
| chr8:109287646
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.823+2105T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287646 | ||||||
| chr8:109287768
|
G | A | 8 | a0001c0001t0001g0342a0003c0003t0003g0176a0003c0003t0003g0177others(5): Show | 8 | HG02135.hp2 HG02451.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1983C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287768 | ||||||
| chr8:109287878
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.823+1873T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287878 | ||||||
| chr8:109287909
|
T | A | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.823+1842A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287909 | ||||||
| chr8:109287917
|
T | A | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823+1834A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287917 | ||||||
| chr8:109287919
|
A | C | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.823+1832T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287919 | ||||||
| chr8:109287978
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+1773G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287978 | ||||||
| chr8:109287999
|
A | G | 3 | a0006c0006t0008g0334a0006c0006t0008g0335a0006c0006t0008g0336 | 3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.823+1752T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109287999 | ||||||
| chr8:109288054
|
A | T | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+1697T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288054 | ||||||
| chr8:109288347
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+1404G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288347 | ||||||
| chr8:109288350
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.823+1401C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288350 | ||||||
| chr8:109288495
|
A | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+1256T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288495 | ||||||
| chr8:109288544
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.823+1207G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288544 | ||||||
| chr8:109288550
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.823+1201T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288550 | ||||||
| chr8:109288719
|
C | T | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+1032G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288719 | ||||||
| chr8:109288911
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.823+840C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288911 | ||||||
| chr8:109288984
|
CT | C | 69 | a0002c0002t0002g0279a0003c0003t0003g0169a0003c0003t0003g0170others(66): Show | 71 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+766delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109288984 | ||||||
| chr8:109289053
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.823+698T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289053 | ||||||
| chr8:109289226
|
A | C | 1 | a0008c0008t0003g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823+525T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289226 | ||||||
| chr8:109289264
|
C | T | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.823+487G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289264 | ||||||
| chr8:109289452
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.823+299G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289452 | ||||||
| chr8:109289506
|
A | C | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+245T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289506 | ||||||
| chr8:109289526
|
A | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.823+225T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289526 | ||||||
| chr8:109289547
|
A | G | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+204T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289547 | ||||||
| chr8:109289606
|
G | T | 1 | a0002c0002t0002g0210 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.823+145C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289606 | ||||||
| chr8:109289637
|
A | T | 1 | a0002c0002t0002g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.823+114T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289637 | ||||||
| chr8:109289715
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.823+36T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289715 | ||||||
| chr8:109289722
|
C | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.823+29G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 5/9 | chr8 | 109289722 | ||||||
| chr8:109290021
|
A | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-88T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290021 | ||||||
| chr8:109290131
|
G | C | 2 | a0002c0002t0002g0243a0002c0002t0002g0282 | 2 | HG01123.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.641-198C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290131 | ||||||
| chr8:109290180
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.641-247A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290180 | ||||||
| chr8:109290191
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.641-258T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290191 | ||||||
| chr8:109290407
|
G | A | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-474C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290407 | ||||||
| chr8:109290478
|
G | A | 5 | a0002c0002t0002g0014a0002c0002t0002g0245a0002c0002t0002g0246others(2): Show | 6 | HG02055.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.641-545C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290478 | ||||||
| chr8:109290522
|
C | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-589G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290522 | ||||||
| chr8:109290566
|
T | C | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-633A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290566 | ||||||
| chr8:109290756
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.641-823A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290756 | ||||||
| chr8:109290764
|
C | G | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-831G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109290764 | ||||||
| chr8:109291105
|
C | T | 1 | a0003c0003t0004g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.641-1172G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291105 | ||||||
| chr8:109291122
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.641-1189A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291122 | ||||||
| chr8:109291137
|
T | C | 1 | a0003c0003t0003g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.641-1204A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291137 | ||||||
| chr8:109291207
|
A | T | 2 | a0008c0008t0003g0182a0008c0008t0003g0197 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-1274T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291207 | ||||||
| chr8:109291218
|
C | T | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.641-1285G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291218 | ||||||
| chr8:109291225
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.641-1292A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291225 | ||||||
| chr8:109291283
|
T | C | 2 | a0002c0002t0002g0277a0002c0002t0002g0278 | 2 | NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.641-1350A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291283 | ||||||
| chr8:109291293
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.641-1360T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291293 | ||||||
| chr8:109291327
|
T | C | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-1394A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291327 | ||||||
| chr8:109291584
|
ACTGTT | A | 21 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(18): Show | 23 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.641-1656_641-1652d others(7): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291584 | ||||||
| chr8:109291598
|
TAAAAAG | T | 24 | a0002c0002t0002g0243a0002c0002t0002g0251a0002c0002t0002g0252others(21): Show | 24 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.641-1671_641-1666d others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291598 | ||||||
| chr8:109291612
|
A | G | 1 | a0002c0002t0015g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.641-1679T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291612 | ||||||
| chr8:109291632
|
A | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-1699T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291632 | ||||||
| chr8:109291639
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.640+1705C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291639 | ||||||
| chr8:109291763
|
A | C | 1 | a0002c0002t0002g0327 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.640+1581T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291763 | ||||||
| chr8:109291780
|
C | T | 5 | a0003c0003t0008g0030a0003c0003t0008g0032a0003c0003t0008g0033others(2): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+1564G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291780 | ||||||
| chr8:109291804
|
C | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG01069.hp2 HG01071.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1540G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291804 | ||||||
| chr8:109291919
|
G | C | 1 | a0002c0002t0002g0271 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.640+1425C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109291919 | ||||||
| chr8:109292019
|
C | T | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+1325G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292019 | ||||||
| chr8:109292193
|
T | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1151A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292193 | ||||||
| chr8:109292216
|
C | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+1128G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292216 | ||||||
| chr8:109292276
|
T | C | 1 | a0004c0004t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.640+1068A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292276 | ||||||
| chr8:109292325
|
A | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.640+1019T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292325 | ||||||
| chr8:109292335
|
C | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+1009G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292335 | ||||||
| chr8:109292357
|
T | C | 1 | a0002c0002t0002g0311 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.640+987A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292357 | ||||||
| chr8:109292434
|
C | CAGAT | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.640+906_640+909dup others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292434 | ||||||
| chr8:109292434
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.640+910G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292434 | ||||||
| chr8:109292518
|
T | A | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.640+826A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292518 | ||||||
| chr8:109292815
|
A | T | 1 | a0003c0003t0003g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.640+529T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292815 | ||||||
| chr8:109292860
|
T | C | 31 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(28): Show | 33 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.640+484A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292860 | ||||||
| chr8:109292968
|
T | C | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+376A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109292968 | ||||||
| chr8:109293053
|
AT | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0063a0001c0001t0001g0118 | 3 | HG02896.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.640+290delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 4/9 | chr8 | 109293053 | ||||||
| chr8:109293707
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.460-183G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109293707 | ||||||
| chr8:109293803
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-279C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109293803 | ||||||
| chr8:109293897
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.460-373A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109293897 | ||||||
| chr8:109294016
|
AAAACACA others(26): Show |
A | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.460-525_460-493del others(33): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294016 | ||||||
| chr8:109294022
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.460-498G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294022 | ||||||
| chr8:109294084
|
CCA | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.460-562_460-561del others(2): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294084 | ||||||
| chr8:109294117
|
T | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-593A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294117 | ||||||
| chr8:109294194
|
G | A | 6 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(3): Show | 6 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-670C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294194 | ||||||
| chr8:109294201
|
AG | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.460-678delC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294201 | ||||||
| chr8:109294269
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.460-745A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294269 | ||||||
| chr8:109294287
|
T | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.460-763A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294287 | ||||||
| chr8:109294325
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.460-801C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294325 | ||||||
| chr8:109294374
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.460-850T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294374 | ||||||
| chr8:109294476
|
GT | G | 29 | a0003c0003t0004g0015a0003c0003t0004g0041a0003c0003t0004g0044others(26): Show | 31 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.460-953delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294476 | ||||||
| chr8:109294489
|
G | T | 1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-965C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294489 | ||||||
| chr8:109294751
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.460-1227G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294751 | ||||||
| chr8:109294845
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0050others(37): Show | 41 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.460-1321C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109294845 | ||||||
| chr8:109295076
|
T | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+1308A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109295076 | ||||||
| chr8:109295165
|
T | G | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+1219A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109295165 | ||||||
| chr8:109295335
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+1049C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109295335 | ||||||
| chr8:109295627
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.459+757C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109295627 | ||||||
| chr8:109296099
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.459+285G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109296099 | ||||||
| chr8:109296344
|
T | G | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459+40A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 3/9 | chr8 | 109296344 | ||||||
| chr8:109296636
|
T | C | 2 | a0002c0002t0002g0313a0002c0002t0002g0331 | 2 | NA18949.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.274-67A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109296636 | ||||||
| chr8:109296950
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.274-381A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109296950 | ||||||
| chr8:109297102
|
T | C | 5 | a0002c0002t0002g0272a0002c0002t0002g0273a0002c0002t0002g0319others(2): Show | 5 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-533A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297102 | ||||||
| chr8:109297153
|
A | G | 32 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(29): Show | 34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.274-584T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297153 | ||||||
| chr8:109297522
|
C | CT | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.274-954dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297522 | ||||||
| chr8:109297535
|
C | T | 3 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0174 | 3 | HG02145.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-966G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297535 | ||||||
| chr8:109297595
|
A | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-1026T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297595 | ||||||
| chr8:109297623
|
T | G | 1 | a0002c0002t0016g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.274-1054A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297623 | ||||||
| chr8:109297730
|
T | C | 33 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(30): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.274-1161A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297730 | ||||||
| chr8:109297867
|
C | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.274-1298G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297867 | ||||||
| chr8:109297883
|
A | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-1314T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297883 | ||||||
| chr8:109297930
|
C | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274-1361G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109297930 | ||||||
| chr8:109298237
|
T | C | 1 | a0002c0002t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.274-1668A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298237 | ||||||
| chr8:109298251
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-1682G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298251 | ||||||
| chr8:109298282
|
T | C | 1 | a0003c0003t0005g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.274-1713A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298282 | ||||||
| chr8:109298450
|
A | T | 1 | a0002c0002t0015g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.274-1881T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298450 | ||||||
| chr8:109298459
|
G | A | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-1890C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298459 | ||||||
| chr8:109298588
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.274-2019C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298588 | ||||||
| chr8:109298670
|
T | A | 2 | a0003c0003t0006g0026a0003c0003t0006g0027 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.274-2101A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298670 | ||||||
| chr8:109298702
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.274-2133T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298702 | ||||||
| chr8:109298865
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.274-2296C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298865 | ||||||
| chr8:109298911
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.274-2342C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298911 | ||||||
| chr8:109298984
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.274-2415G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109298984 | ||||||
| chr8:109299035
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274-2466C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299035 | ||||||
| chr8:109299175
|
C | G | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-2606G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299175 | ||||||
| chr8:109299217
|
T | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-2648A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299217 | ||||||
| chr8:109299408
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-2839G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299408 | ||||||
| chr8:109299409
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-2840T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299409 | ||||||
| chr8:109299628
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.274-3059G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299628 | ||||||
| chr8:109299697
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.274-3128G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299697 | ||||||
| chr8:109299810
|
G | T | 11 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0219others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-3241C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299810 | ||||||
| chr8:109299893
|
T | C | 1 | a0003c0003t0006g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.274-3324A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299893 | ||||||
| chr8:109299967
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-3398A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109299967 | ||||||
| chr8:109300018
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.274-3449G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300018 | ||||||
| chr8:109300019
|
G | A | 15 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(12): Show | 16 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.274-3450C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300019 | ||||||
| chr8:109300140
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0124 | 2 | NA19001.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.274-3571G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300140 | ||||||
| chr8:109300204
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.274-3635A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300204 | ||||||
| chr8:109300343
|
CA | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-3775delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300343 | ||||||
| chr8:109300561
|
A | G | 8 | a0003c0003t0004g0015a0003c0003t0004g0338a0003c0003t0004g0339others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-3992T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300561 | ||||||
| chr8:109300734
|
C | G | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.274-4165G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300734 | ||||||
| chr8:109300735
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.274-4166T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109300735 | ||||||
| chr8:109301021
|
GAC | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.274-4454_274-4453d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301021 | ||||||
| chr8:109301284
|
C | T | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-4715G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301284 | ||||||
| chr8:109301346
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-4777T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301346 | ||||||
| chr8:109301489
|
C | G | 3 | a0003c0003t0003g0036a0003c0003t0003g0037a0003c0003t0003g0040 | 3 | HG02615.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.274-4920G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301489 | ||||||
| chr8:109301590
|
C | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-5021G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301590 | ||||||
| chr8:109301591
|
G | A | 9 | a0003c0003t0003g0170a0003c0003t0003g0185a0003c0003t0003g0186others(6): Show | 9 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-5022C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301591 | ||||||
| chr8:109301655
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-5086A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301655 | ||||||
| chr8:109301810
|
G | A | 2 | a0002c0002t0002g0274a0002c0002t0002g0275 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.274-5241C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301810 | ||||||
| chr8:109301830
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-5261G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301830 | ||||||
| chr8:109301901
|
C | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-5332G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301901 | ||||||
| chr8:109301953
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-5384A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109301953 | ||||||
| chr8:109302085
|
T | C | 2 | a0002c0002t0002g0287a0002c0002t0002g0315 | 2 | NA18944.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.274-5516A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302085 | ||||||
| chr8:109302360
|
A | G | 2 | a0002c0002t0002g0294a0002c0002t0002g0295 | 2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.274-5791T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302360 | ||||||
| chr8:109302382
|
C | T | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.274-5813G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302382 | ||||||
| chr8:109302462
|
T | A | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.274-5893A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302462 | ||||||
| chr8:109302486
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.274-5917A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302486 | ||||||
| chr8:109302609
|
C | A | 2 | a0005c0005t0007g0171a0005c0005t0007g0174 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-6040G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302609 | ||||||
| chr8:109302715
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.274-6146T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302715 | ||||||
| chr8:109302793
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.274-6224C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302793 | ||||||
| chr8:109302835
|
A | G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-6266T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302835 | ||||||
| chr8:109302927
|
G | A | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-6358C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302927 | ||||||
| chr8:109302969
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.274-6400C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302969 | ||||||
| chr8:109302983
|
A | T | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274-6414T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109302983 | ||||||
| chr8:109303294
|
C | T | 1 | a0002c0002t0002g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.274-6725G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303294 | ||||||
| chr8:109303351
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-6782C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303351 | ||||||
| chr8:109303382
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.274-6813A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303382 | ||||||
| chr8:109303390
|
A | G | 20 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0213others(17): Show | 22 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.274-6821T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303390 | ||||||
| chr8:109303456
|
G | A | 1 | a0003c0003t0003g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.274-6887C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303456 | ||||||
| chr8:109303488
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.274-6919G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303488 | ||||||
| chr8:109303528
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.274-6959A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303528 | ||||||
| chr8:109303533
|
G | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.274-6964C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303533 | ||||||
| chr8:109303549
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-6980A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303549 | ||||||
| chr8:109303555
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-6986C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303555 | ||||||
| chr8:109303608
|
T | C | 1 | a0003c0003t0003g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.274-7039A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303608 | ||||||
| chr8:109303614
|
GCTACAGC others(36): Show |
G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-7088_274-7046d others(45): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303614 | ||||||
| chr8:109303662
|
T | C | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-7093A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303662 | ||||||
| chr8:109303740
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-7171G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303740 | ||||||
| chr8:109303843
|
C | T | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-7274G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109303843 | ||||||
| chr8:109304146
|
C | T | 2 | a0002c0002t0002g0277a0002c0002t0002g0278 | 2 | NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.274-7577G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304146 | ||||||
| chr8:109304213
|
C | T | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-7644G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304213 | ||||||
| chr8:109304214
|
G | A | 1 | a0002c0002t0002g0324 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.274-7645C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304214 | ||||||
| chr8:109304467
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-7898G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304467 | ||||||
| chr8:109304484
|
T | C | 1 | a0003c0003t0004g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274-7915A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304484 | ||||||
| chr8:109304579
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.274-8010C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304579 | ||||||
| chr8:109304622
|
G | A | 2 | a0003c0003t0006g0042a0003c0003t0006g0043 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.274-8053C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304622 | ||||||
| chr8:109304774
|
C | T | 2 | a0002c0002t0002g0249a0002c0002t0002g0250 | 2 | HG00597.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.274-8205G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304774 | ||||||
| chr8:109304800
|
A | C | 1 | a0001c0001t0018g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-8231T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109304800 | ||||||
| chr8:109305034
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.274-8465A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305034 | ||||||
| chr8:109305105
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.274-8536C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305105 | ||||||
| chr8:109305200
|
A | G | 30 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(27): Show | 30 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.274-8631T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305200 | ||||||
| chr8:109305415
|
A | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.274-8846T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305415 | ||||||
| chr8:109305424
|
C | A | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-8855G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305424 | ||||||
| chr8:109305459
|
G | A | 5 | a0003c0003t0003g0178a0003c0003t0003g0179a0003c0003t0003g0180others(2): Show | 5 | NA18970.hp2 NA18981.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-8890C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305459 | ||||||
| chr8:109305466
|
T | C | 1 | a0002c0002t0002g0276 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.274-8897A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305466 | ||||||
| chr8:109305484
|
C | T | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-8915G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305484 | ||||||
| chr8:109305506
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.274-8937C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305506 | ||||||
| chr8:109305512
|
A | C | 1 | a0005c0005t0007g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-8943T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305512 | ||||||
| chr8:109305566
|
C | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274-8997G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305566 | ||||||
| chr8:109305734
|
C | G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-9165G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305734 | ||||||
| chr8:109305776
|
T | A | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274-9207A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305776 | ||||||
| chr8:109305926
|
G | A | 2 | a0008c0008t0003g0182a0008c0008t0003g0197 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.274-9357C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305926 | ||||||
| chr8:109305961
|
C | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.274-9392G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109305961 | ||||||
| chr8:109306202
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0063a0001c0001t0001g0118 | 3 | HG02896.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.274-9633G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306202 | ||||||
| chr8:109306257
|
G | C | 1 | a0003c0003t0006g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.274-9688C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306257 | ||||||
| chr8:109306387
|
C | T | 1 | a0004c0004t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.274-9818G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306387 | ||||||
| chr8:109306462
|
G | A | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-9893C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306462 | ||||||
| chr8:109306515
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.274-9946A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306515 | ||||||
| chr8:109306562
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.274-9993A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306562 | ||||||
| chr8:109306566
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.274-9997T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306566 | ||||||
| chr8:109306572
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.274-10003T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306572 | ||||||
| chr8:109306631
|
A | AC | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.274-10063dupG | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306631 | ||||||
| chr8:109306631
|
A | C | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.274-10062T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306631 | ||||||
| chr8:109306639
|
C | G | 1 | a0003c0003t0005g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274-10070G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306639 | ||||||
| chr8:109306640
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.274-10071T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306640 | ||||||
| chr8:109306672
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.274-10103A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306672 | ||||||
| chr8:109306803
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-10234G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306803 | ||||||
| chr8:109306850
|
A | G | 3 | a0002c0002t0002g0319a0002c0002t0002g0320a0002c0002t0002g0321 | 3 | HG00558.hp1 HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.274-10281T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306850 | ||||||
| chr8:109306907
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-10338G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306907 | ||||||
| chr8:109306956
|
C | A | 1 | a0003c0003t0004g0337 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.274-10387G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109306956 | ||||||
| chr8:109307063
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.274-10494A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307063 | ||||||
| chr8:109307132
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02129.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.274-10563C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307132 | ||||||
| chr8:109307136
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.274-10567T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307136 | ||||||
| chr8:109307349
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274-10780G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307349 | ||||||
| chr8:109307389
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.274-10820T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307389 | ||||||
| chr8:109307476
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.274-10907A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307476 | ||||||
| chr8:109307696
|
A | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-11127T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307696 | ||||||
| chr8:109307864
|
A | T | 1 | a0002c0002t0002g0242 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.274-11295T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307864 | ||||||
| chr8:109307948
|
A | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274-11379T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109307948 | ||||||
| chr8:109308445
|
C | G | 1 | a0001c0001t0001g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.274-11876G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308445 | ||||||
| chr8:109308719
|
C | T | 1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.274-12150G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308719 | ||||||
| chr8:109308800
|
T | C | 76 | a0002c0002t0008g0333a0003c0003t0003g0169a0003c0003t0003g0170others(73): Show | 79 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.274-12231A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308800 | ||||||
| chr8:109308840
|
CAG | C | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-12273_274-1227 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308840 | ||||||
| chr8:109308850
|
T | C | 5 | a0002c0002t0002g0277a0002c0002t0002g0278a0002c0002t0002g0284others(2): Show | 5 | HG02040.hp1 HG02135.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-12281A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308850 | ||||||
| chr8:109308910
|
T | C | 30 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(27): Show | 32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.274-12341A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308910 | ||||||
| chr8:109308971
|
CA | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.274-12403delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308971 | ||||||
| chr8:109308971
|
CAA | C | 12 | a0003c0003t0003g0185a0003c0003t0004g0219a0003c0003t0004g0341others(9): Show | 12 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-12404_274-1240 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109308971 | ||||||
| chr8:109309042
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0051others(34): Show | 40 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.274-12473A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309042 | ||||||
| chr8:109309097
|
C | T | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-12528G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309097 | ||||||
| chr8:109309180
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.274-12611A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309180 | ||||||
| chr8:109309367
|
T | C | 1 | a0004c0004t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.274-12798A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309367 | ||||||
| chr8:109309439
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.273+12870A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309439 | ||||||
| chr8:109309551
|
A | G | 1 | a0008c0008t0003g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.273+12758T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309551 | ||||||
| chr8:109309653
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0157 | 2 | NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.273+12656C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309653 | ||||||
| chr8:109309686
|
A | G | 1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.273+12623T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309686 | ||||||
| chr8:109309830
|
C | A | 1 | a0002c0002t0002g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+12479G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309830 | ||||||
| chr8:109309877
|
C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.273+12432G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309877 | ||||||
| chr8:109309878
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.273+12431T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309878 | ||||||
| chr8:109309956
|
C | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.273+12353G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109309956 | ||||||
| chr8:109310090
|
T | C | 30 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(27): Show | 30 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.273+12219A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310090 | ||||||
| chr8:109310187
|
A | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.273+12122T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310187 | ||||||
| chr8:109310216
|
C | G | 1 | a0002c0002t0002g0311 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.273+12093G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310216 | ||||||
| chr8:109310226
|
A | C | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+12083T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310226 | ||||||
| chr8:109310393
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.273+11916C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310393 | ||||||
| chr8:109310580
|
C | T | 1 | a0003c0003t0003g0184 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.273+11729G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310580 | ||||||
| chr8:109310741
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.273+11568T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310741 | ||||||
| chr8:109310810
|
C | CT | 66 | a0002c0002t0002g0228a0002c0002t0002g0237a0002c0002t0002g0245others(63): Show | 67 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.273+11498dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310810 | ||||||
| chr8:109310810
|
CT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.273+11498delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310810 | ||||||
| chr8:109310849
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.273+11460A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310849 | ||||||
| chr8:109310867
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.273+11442C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310867 | ||||||
| chr8:109310869
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0001g0150 | 3 | NA19004.hp1 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.273+11440C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310869 | ||||||
| chr8:109310885
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0151 | 3 | HG01069.hp1 HG01074.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.273+11424C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310885 | ||||||
| chr8:109310960
|
C | A | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+11349G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109310960 | ||||||
| chr8:109311028
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0051others(34): Show | 40 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.273+11281T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311028 | ||||||
| chr8:109311029
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.273+11280G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311029 | ||||||
| chr8:109311030
|
G | A | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+11279C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311030 | ||||||
| chr8:109311049
|
T | A | 1 | a0002c0002t0002g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.273+11260A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311049 | ||||||
| chr8:109311060
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+11249A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311060 | ||||||
| chr8:109311089
|
C | T | 1 | a0003c0003t0003g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.273+11220G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311089 | ||||||
| chr8:109311107
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.273+11202G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311107 | ||||||
| chr8:109311154
|
A | C | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+11155T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311154 | ||||||
| chr8:109311180
|
C | T | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+11129G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311180 | ||||||
| chr8:109311220
|
A | G | 63 | a0002c0002t0008g0333a0003c0003t0003g0169a0003c0003t0003g0170others(60): Show | 65 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.273+11089T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311220 | ||||||
| chr8:109311282
|
C | T | 2 | a0002c0002t0002g0244a0002c0002t0002g0328 | 2 | NA18955.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.273+11027G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311282 | ||||||
| chr8:109311291
|
T | C | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+11018A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311291 | ||||||
| chr8:109311386
|
A | T | 1 | a0004c0004t0009g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.273+10923T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311386 | ||||||
| chr8:109311556
|
G | GATATATA others(17): Show |
2 | a0005c0005t0007g0202a0005c0005t0007g0203 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.273+10752_273+1075 others(28): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311556
|
G | GATATATA others(27): Show |
1 | a0005c0005t0007g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.273+10752_273+1075 others(38): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311556
|
G | GATATATA others(29): Show |
1 | a0005c0005t0007g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.273+10752_273+1075 others(40): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311556
|
G | GATATATA others(31): Show |
1 | a0005c0005t0007g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.273+10752_273+1075 others(42): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311556
|
G | GATATATA others(33): Show |
2 | a0005c0005t0007g0207a0005c0005t0007g0208 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.273+10752_273+1075 others(44): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311556
|
G | GATATATA others(35): Show |
2 | a0005c0005t0007g0172a0005c0005t0007g0201 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.273+10752_273+1075 others(46): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311556 | ||||||
| chr8:109311557
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+10752C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311557 | ||||||
| chr8:109311557
|
G | GTATATAT others(9): Show |
7 | a0003c0003t0003g0170a0003c0003t0003g0185a0003c0003t0003g0186others(4): Show | 7 | HG00741.hp2 HG01123.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+10751_273+1075 others(20): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311557 | ||||||
| chr8:109311557
|
G | GTATATAT others(11): Show |
2 | a0003c0003t0003g0190a0003c0003t0003g0191 | 2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.273+10751_273+1075 others(22): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311557 | ||||||
| chr8:109311559
|
G | A | 18 | a0003c0003t0003g0170a0003c0003t0003g0185a0003c0003t0003g0186others(15): Show | 18 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.273+10750C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATA | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.273+10746_273+1074 others(8): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(3): Show |
1 | a0003c0003t0003g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273+10740_273+1074 others(14): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(17): Show |
1 | a0003c0003t0003g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(28): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(23): Show |
1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(34): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(27): Show |
2 | a0003c0003t0003g0193a0003c0003t0003g0199 | 2 | HG02886.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(38): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(31): Show |
3 | a0003c0003t0003g0169a0003c0003t0003g0176a0003c0003t0003g0177 | 3 | HG01167.hp2 HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(42): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(33): Show |
5 | a0003c0003t0003g0178a0003c0003t0003g0179a0003c0003t0003g0194others(2): Show | 5 | HG02280.hp1 NA18970.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(44): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(35): Show |
4 | a0003c0003t0003g0180a0003c0003t0003g0181a0003c0003t0003g0184others(1): Show | 4 | HG01496.hp1 HG03490.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(46): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(37): Show |
2 | a0008c0008t0003g0182a0008c0008t0003g0197 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(48): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(39): Show |
1 | a0003c0003t0003g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(50): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(41): Show |
1 | a0003c0003t0003g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(52): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTATATAT others(47): Show |
1 | a0003c0003t0003g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(58): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(5): Show |
112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(16): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(7): Show |
9 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(18): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(9): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0068a0003c0003t0003g0035others(1): Show | 5 | HG01192.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(20): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(11): Show |
4 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(22): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(13): Show |
3 | a0003c0003t0006g0042a0003c0003t0006g0343a0009c0009t0012g0048 | 3 | HG02257.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(24): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(25): Show |
1 | a0003c0003t0003g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(36): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(27): Show |
4 | a0001c0001t0001g0342a0003c0003t0003g0037a0003c0003t0003g0040others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(38): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(35): Show |
1 | a0003c0003t0004g0219 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(46): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(37): Show |
2 | a0003c0003t0004g0015a0003c0003t0004g0339 | 3 | HG02976.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(48): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(39): Show |
1 | a0003c0003t0003g0221 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(50): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(41): Show |
3 | a0006c0006t0008g0334a0006c0006t0008g0335a0006c0006t0008g0336 | 3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(52): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(45): Show |
1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(56): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(47): Show |
1 | a0003c0003t0003g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(58): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTATAT others(49): Show |
1 | a0003c0003t0004g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(60): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(23): Show |
2 | a0004c0004t0009g0163a0004c0004t0009g0166 | 2 | HG02683.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(34): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(29): Show |
1 | a0004c0004t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(40): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(31): Show |
2 | a0003c0003t0004g0337a0004c0004t0001g0140 | 2 | HG04204.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(42): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(35): Show |
2 | a0004c0004t0001g0141a0004c0004t0001g0160 | 2 | HG01106.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(46): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(43): Show |
2 | a0002c0002t0008g0333a0004c0004t0001g0062 | 2 | HG02055.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(54): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(45): Show |
1 | a0004c0004t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(56): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(47): Show |
3 | a0003c0003t0004g0345a0004c0004t0009g0008a0004c0004t0009g0164 | 4 | HG02622.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+10749_273+1075 others(58): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(49): Show |
2 | a0004c0004t0001g0161a0004c0004t0001g0162 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(60): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTAT others(61): Show |
1 | a0004c0004t0009g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(72): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(11): Show |
1 | a0003c0003t0004g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(22): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(15): Show |
1 | a0003c0003t0004g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(26): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(33): Show |
1 | a0003c0003t0004g0045 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(44): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(37): Show |
1 | a0003c0003t0004g0047 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(48): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(39): Show |
1 | a0003c0003t0004g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(50): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(53): Show |
1 | a0003c0003t0004g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(64): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(37): Show |
2 | a0003c0003t0004g0214a0003c0003t0004g0215 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(48): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(41): Show |
2 | a0003c0003t0004g0218a0003c0003t0006g0009 | 3 | HG01884.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.273+10749_273+1075 others(52): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(43): Show |
1 | a0003c0003t0004g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(54): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(45): Show |
1 | a0003c0003t0006g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(56): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(49): Show |
1 | a0003c0003t0004g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273+10749_273+1075 others(60): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311559
|
G | GTGTGTGT others(35): Show |
1 | a0003c0003t0004g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+10749_273+1075 others(46): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311559 | ||||||
| chr8:109311786
|
G | A | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.273+10523C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109311786 | ||||||
| chr8:109312021
|
G | A | 2 | a0002c0002t0002g0239a0009c0009t0012g0048 | 2 | HG02257.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.273+10288C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312021 | ||||||
| chr8:109312077
|
C | T | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.273+10232G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312077 | ||||||
| chr8:109312104
|
C | T | 1 | a0003c0003t0004g0340 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+10205G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312104 | ||||||
| chr8:109312203
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.273+10106C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312203 | ||||||
| chr8:109312226
|
C | A | 2 | a0002c0002t0002g0294a0002c0002t0002g0295 | 2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.273+10083G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312226 | ||||||
| chr8:109312276
|
G | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(8): Show | 11 | HG02071.hp1 HG02523.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+10033C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312276 | ||||||
| chr8:109312293
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+10016T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312293 | ||||||
| chr8:109312298
|
C | CA | 33 | a0002c0002t0002g0238a0002c0002t0002g0242a0002c0002t0002g0280others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+10010dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312298 | ||||||
| chr8:109312298
|
CA | C | 30 | a0001c0001t0001g0016a0001c0001t0001g0070a0001c0001t0001g0097others(27): Show | 31 | HG00741.hp1 HG01167.hp1 HG01978.hp2 others(28): Show |
intron_variant | MODIFIER | c.273+10010delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312298 | ||||||
| chr8:109312298
|
CAA | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.273+10009_273+1001 others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312298 | ||||||
| chr8:109312427
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.273+9882A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312427 | ||||||
| chr8:109312479
|
T | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+9830A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312479 | ||||||
| chr8:109312492
|
T | C | 14 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(11): Show | 15 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.273+9817A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312492 | ||||||
| chr8:109312522
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.273+9787A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312522 | ||||||
| chr8:109312590
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.273+9719G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312590 | ||||||
| chr8:109312602
|
GTTTA | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 77 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.273+9703_273+9706d others(6): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312602 | ||||||
| chr8:109312625
|
A | G | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+9684T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312625 | ||||||
| chr8:109312718
|
C | T | 1 | a0004c0004t0001g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.273+9591G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109312718 | ||||||
| chr8:109313127
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+9182G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313127 | ||||||
| chr8:109313244
|
C | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+9065G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313244 | ||||||
| chr8:109313317
|
C | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.273+8992G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313317 | ||||||
| chr8:109313318
|
G | T | 1 | a0004c0004t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.273+8991C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313318 | ||||||
| chr8:109313433
|
T | C | 1 | a0002c0002t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.273+8876A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313433 | ||||||
| chr8:109313539
|
A | C | 2 | a0002c0002t0002g0243a0002c0002t0002g0282 | 2 | HG01123.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.273+8770T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313539 | ||||||
| chr8:109313541
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.273+8768A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313541 | ||||||
| chr8:109313560
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.273+8749A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313560 | ||||||
| chr8:109313583
|
G | A | 1 | a0003c0003t0004g0041 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.273+8726C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313583 | ||||||
| chr8:109313596
|
T | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+8713A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313596 | ||||||
| chr8:109313607
|
T | C | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+8702A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313607 | ||||||
| chr8:109313650
|
G | C | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+8659C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313650 | ||||||
| chr8:109313740
|
A | G | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+8569T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109313740 | ||||||
| chr8:109314030
|
T | C | 1 | a0002c0002t0002g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.273+8279A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314030 | ||||||
| chr8:109314052
|
A | T | 5 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070others(2): Show | 5 | HG02040.hp2 NA18966.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+8257T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314052 | ||||||
| chr8:109314081
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.273+8228C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314081 | ||||||
| chr8:109314103
|
C | A | 1 | a0002c0002t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.273+8206G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314103 | ||||||
| chr8:109314109
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.273+8200A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314109 | ||||||
| chr8:109314166
|
A | C | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+8143T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314166 | ||||||
| chr8:109314172
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 5 | HG00280.hp2 HG01192.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+8137G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314172 | ||||||
| chr8:109314259
|
C | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.273+8050G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314259 | ||||||
| chr8:109314449
|
A | T | 1 | a0003c0003t0003g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.273+7860T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314449 | ||||||
| chr8:109314450
|
T | A | 1 | a0003c0003t0003g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.273+7859A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314450 | ||||||
| chr8:109314880
|
A | C | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+7429T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314880 | ||||||
| chr8:109314894
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02451.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.273+7415C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314894 | ||||||
| chr8:109314919
|
T | G | 2 | a0002c0002t0002g0308a0002c0002t0002g0309 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.273+7390A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109314919 | ||||||
| chr8:109315185
|
A | AT | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.273+7123dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315185 | ||||||
| chr8:109315209
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0144others(3): Show | 6 | HG00735.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7100G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315209 | ||||||
| chr8:109315549
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+6760T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315549 | ||||||
| chr8:109315822
|
G | A | 3 | a0002c0002t0002g0228a0002c0002t0002g0229a0002c0002t0016g0230 | 3 | HG00735.hp1 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.273+6487C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315822 | ||||||
| chr8:109315887
|
T | G | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02071.hp1 HG02523.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+6422A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315887 | ||||||
| chr8:109315948
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.273+6361A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315948 | ||||||
| chr8:109315953
|
C | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6356G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315953 | ||||||
| chr8:109315955
|
T | TCA | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+6352_273+6353d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109315955 | ||||||
| chr8:109316128
|
C | G | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+6181G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316128 | ||||||
| chr8:109316169
|
G | T | 1 | a0002c0002t0002g0242 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.273+6140C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316169 | ||||||
| chr8:109316488
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+5821C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316488 | ||||||
| chr8:109316537
|
T | A | 1 | a0002c0002t0002g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.273+5772A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316537 | ||||||
| chr8:109316621
|
C | A | 4 | a0003c0003t0004g0044a0003c0003t0004g0045a0003c0003t0004g0046others(1): Show | 4 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+5688G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316621 | ||||||
| chr8:109316710
|
C | A | 1 | a0002c0002t0002g0311 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.273+5599G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316710 | ||||||
| chr8:109316710
|
C | T | 1 | a0002c0002t0002g0241 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.273+5599G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316710 | ||||||
| chr8:109316770
|
G | A | 2 | a0002c0002t0002g0284a0002c0002t0002g0285 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.273+5539C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316770 | ||||||
| chr8:109316783
|
T | G | 3 | a0006c0006t0008g0334a0006c0006t0008g0335a0006c0006t0008g0336 | 3 | HG01884.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.273+5526A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316783 | ||||||
| chr8:109316797
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.273+5512G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316797 | ||||||
| chr8:109316819
|
T | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0135 | 2 | NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.273+5490A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316819 | ||||||
| chr8:109316940
|
T | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.273+5369A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109316940 | ||||||
| chr8:109317062
|
C | T | 8 | a0003c0003t0004g0213a0003c0003t0004g0214a0003c0003t0004g0215others(5): Show | 9 | HG01243.hp1 HG01884.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+5247G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317062 | ||||||
| chr8:109317132
|
A | G | 1 | a0008c0008t0003g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.273+5177T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317132 | ||||||
| chr8:109317290
|
C | T | 1 | a0002c0002t0002g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.273+5019G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317290 | ||||||
| chr8:109317311
|
T | C | 1 | a0004c0004t0009g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.273+4998A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317311 | ||||||
| chr8:109317367
|
C | A | 1 | a0003c0003t0006g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+4942G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317367 | ||||||
| chr8:109317403
|
G | C | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+4906C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317403 | ||||||
| chr8:109317488
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+4821C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317488 | ||||||
| chr8:109317552
|
AGGATCCA others(9): Show |
A | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+4741_273+4756d others(18): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317552 | ||||||
| chr8:109317647
|
G | C | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+4662C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317647 | ||||||
| chr8:109317789
|
C | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.273+4520G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317789 | ||||||
| chr8:109317900
|
C | G | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+4409G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317900 | ||||||
| chr8:109317906
|
T | C | 33 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(30): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+4403A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317906 | ||||||
| chr8:109317939
|
G | A | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.273+4370C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317939 | ||||||
| chr8:109317964
|
G | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+4345C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317964 | ||||||
| chr8:109317983
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+4326A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109317983 | ||||||
| chr8:109318047
|
T | G | 1 | a0004c0004t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.273+4262A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318047 | ||||||
| chr8:109318130
|
T | A | 2 | a0003c0003t0004g0044a0003c0003t0004g0046 | 2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.273+4179A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318130 | ||||||
| chr8:109318163
|
C | T | 3 | a0002c0002t0002g0204a0002c0002t0002g0239a0002c0002t0002g0240 | 3 | HG00639.hp2 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.273+4146G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318163 | ||||||
| chr8:109318206
|
C | T | 8 | a0003c0003t0004g0213a0003c0003t0004g0214a0003c0003t0004g0215others(5): Show | 9 | HG01243.hp1 HG01884.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+4103G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318206 | ||||||
| chr8:109318245
|
T | C | 1 | a0002c0002t0002g0286 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.273+4064A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318245 | ||||||
| chr8:109318262
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.273+4047T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318262 | ||||||
| chr8:109318307
|
G | C | 1 | a0002c0002t0002g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+4002C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318307 | ||||||
| chr8:109318357
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+3952G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318357 | ||||||
| chr8:109318567
|
G | A | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.273+3742C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318567 | ||||||
| chr8:109318594
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273+3715A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318594 | ||||||
| chr8:109318619
|
T | TC | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.273+3689_273+3690i others(3): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318619 | ||||||
| chr8:109318664
|
T | C | 1 | a0003c0003t0004g0047 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.273+3645A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318664 | ||||||
| chr8:109318745
|
T | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+3564A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318745 | ||||||
| chr8:109318830
|
T | C | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+3479A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318830 | ||||||
| chr8:109318864
|
A | G | 30 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(27): Show | 30 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.273+3445T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318864 | ||||||
| chr8:109318958
|
G | GT | 6 | a0002c0002t0002g0235a0002c0002t0002g0237a0002c0002t0002g0238others(3): Show | 6 | HG00438.hp1 HG01109.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+3350dupA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318958 | ||||||
| chr8:109318958
|
GT | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.273+3350delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318958 | ||||||
| chr8:109318958
|
GTT | G | 30 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(27): Show | 30 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.273+3349_273+3350d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318958 | ||||||
| chr8:109318980
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.273+3329G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318980 | ||||||
| chr8:109318995
|
T | C | 1 | a0006c0006t0008g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.273+3314A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109318995 | ||||||
| chr8:109319085
|
T | C | 1 | a0003c0003t0004g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.273+3224A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319085 | ||||||
| chr8:109319091
|
A | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+3218T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319091 | ||||||
| chr8:109319173
|
T | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+3136A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319173 | ||||||
| chr8:109319174
|
C | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+3135G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319174 | ||||||
| chr8:109319217
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.273+3092G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319217 | ||||||
| chr8:109319253
|
G | A | 1 | a0002c0002t0002g0297 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.273+3056C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319253 | ||||||
| chr8:109319269
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.273+3040C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319269 | ||||||
| chr8:109319439
|
C | T | 3 | a0002c0002t0002g0296a0002c0002t0002g0297a0002c0002t0002g0316 | 3 | NA18952.hp1 NA18954.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.273+2870G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319439 | ||||||
| chr8:109319536
|
T | C | 6 | a0002c0002t0002g0235a0002c0002t0002g0236a0002c0002t0002g0287others(3): Show | 7 | HG00438.hp1 HG00558.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+2773A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319536 | ||||||
| chr8:109319738
|
G | A | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273+2571C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319738 | ||||||
| chr8:109319876
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.273+2433C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319876 | ||||||
| chr8:109319929
|
T | A | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.273+2380A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319929 | ||||||
| chr8:109319931
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.273+2378T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109319931 | ||||||
| chr8:109320010
|
G | A | 1 | a0002c0002t0002g0301 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.273+2299C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320010 | ||||||
| chr8:109320144
|
T | C | 5 | a0004c0004t0009g0008a0004c0004t0009g0163a0004c0004t0009g0164others(2): Show | 6 | HG00280.hp1 HG02683.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+2165A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320144 | ||||||
| chr8:109320150
|
T | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+2159A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320150 | ||||||
| chr8:109320173
|
A | G | 33 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(30): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+2136T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320173 | ||||||
| chr8:109320453
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+1856C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320453 | ||||||
| chr8:109320806
|
G | A | 1 | a0005c0005t0007g0203 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+1503C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320806 | ||||||
| chr8:109320859
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+1450C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320859 | ||||||
| chr8:109320909
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.273+1400G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320909 | ||||||
| chr8:109320978
|
T | C | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+1331A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109320978 | ||||||
| chr8:109321143
|
C | T | 7 | a0003c0003t0003g0176a0003c0003t0003g0177a0003c0003t0003g0178others(4): Show | 7 | HG02135.hp2 NA18950.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+1166G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321143 | ||||||
| chr8:109321144
|
G | A | 4 | a0002c0002t0002g0288a0002c0002t0002g0289a0002c0002t0002g0290others(1): Show | 4 | NA18747.hp2 NA19076.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+1165C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321144 | ||||||
| chr8:109321185
|
G | A | 4 | a0003c0003t0004g0044a0003c0003t0004g0045a0003c0003t0004g0046others(1): Show | 4 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1124C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321185 | ||||||
| chr8:109321224
|
T | G | 1 | a0003c0003t0006g0009 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.273+1085A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321224 | ||||||
| chr8:109321301
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273+1008T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321301 | ||||||
| chr8:109321319
|
A | G | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+990T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321319 | ||||||
| chr8:109321495
|
A | T | 1 | a0002c0002t0002g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.273+814T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321495 | ||||||
| chr8:109321496
|
A | T | 1 | a0002c0002t0002g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.273+813T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321496 | ||||||
| chr8:109321513
|
AT | A | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.273+795delA | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321513 | ||||||
| chr8:109321558
|
A | T | 1 | a0003c0003t0003g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.273+751T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321558 | ||||||
| chr8:109321615
|
G | C | 5 | a0004c0004t0009g0008a0004c0004t0009g0163a0004c0004t0009g0164others(2): Show | 6 | HG00280.hp1 HG02683.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+694C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321615 | ||||||
| chr8:109321625
|
T | A | 1 | a0003c0003t0003g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.273+684A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321625 | ||||||
| chr8:109321780
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+529T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109321780 | ||||||
| chr8:109322095
|
T | C | 1 | a0004c0004t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+214A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 2/9 | chr8 | 109322095 | ||||||
| chr8:109322695
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.119-232C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109322695 | ||||||
| chr8:109322767
|
CAG | C | 14 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(11): Show | 15 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-306_119-305del others(2): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109322767 | ||||||
| chr8:109322853
|
T | TAA | 30 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(27): Show | 32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.119-392_119-391dup others(2): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109322853 | ||||||
| chr8:109322857
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119-394T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109322857 | ||||||
| chr8:109322866
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119-403A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109322866 | ||||||
| chr8:109323089
|
T | C | 8 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0219others(5): Show | 9 | HG02055.hp1 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-626A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323089 | ||||||
| chr8:109323156
|
G | A | 30 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(27): Show | 32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.119-693C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323156 | ||||||
| chr8:109323274
|
T | C | 1 | a0003c0003t0008g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.119-811A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323274 | ||||||
| chr8:109323298
|
C | T | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.119-835G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323298 | ||||||
| chr8:109323397
|
T | C | 4 | a0003c0003t0004g0044a0003c0003t0004g0045a0003c0003t0004g0046others(1): Show | 4 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-934A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323397 | ||||||
| chr8:109323505
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119-1042T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323505 | ||||||
| chr8:109323836
|
G | C | 4 | a0003c0003t0003g0035a0003c0003t0003g0036a0003c0003t0003g0037others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-1373C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323836 | ||||||
| chr8:109323916
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.119-1453A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323916 | ||||||
| chr8:109323947
|
C | A | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-1484G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109323947 | ||||||
| chr8:109324202
|
G | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-1739C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324202 | ||||||
| chr8:109324203
|
C | CA | 10 | a0003c0003t0004g0345a0005c0005t0007g0171a0005c0005t0007g0172others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-1741dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324203 | ||||||
| chr8:109324245
|
A | G | 2 | a0003c0003t0006g0009a0003c0003t0006g0212 | 3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.119-1782T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324245 | ||||||
| chr8:109324373
|
T | C | 13 | a0004c0004t0001g0062a0004c0004t0001g0140a0004c0004t0001g0141others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-1910A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324373 | ||||||
| chr8:109324393
|
C | CA | 8 | a0001c0001t0001g0143a0003c0003t0008g0032a0003c0003t0008g0033others(5): Show | 8 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-1931dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324393 | ||||||
| chr8:109324393
|
CA | C | 12 | a0001c0001t0001g0342a0002c0002t0002g0235a0002c0002t0002g0236others(9): Show | 14 | HG00438.hp1 HG00558.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-1931delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324393 | ||||||
| chr8:109324407
|
A | G | 1 | a0007c0007t0001g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-1944T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324407 | ||||||
| chr8:109324443
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.119-1980A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324443 | ||||||
| chr8:109324474
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.119-2011A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324474 | ||||||
| chr8:109324652
|
G | A | 1 | a0002c0002t0002g0292 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.119-2189C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324652 | ||||||
| chr8:109324858
|
G | T | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-2395C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324858 | ||||||
| chr8:109324877
|
G | A | 30 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(27): Show | 32 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.119-2414C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324877 | ||||||
| chr8:109324983
|
G | C | 1 | a0003c0003t0006g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.119-2520C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109324983 | ||||||
| chr8:109325041
|
G | A | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-2578C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325041 | ||||||
| chr8:109325095
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.119-2632T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325095 | ||||||
| chr8:109325179
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.119-2716T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325179 | ||||||
| chr8:109325203
|
G | A | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.119-2740C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325203 | ||||||
| chr8:109325428
|
C | T | 7 | a0002c0002t0002g0296a0002c0002t0002g0297a0002c0002t0002g0298others(4): Show | 7 | HG00597.hp1 HG00621.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-2965G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325428 | ||||||
| chr8:109325469
|
T | G | 7 | a0003c0003t0006g0026a0003c0003t0006g0027a0003c0003t0006g0028others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-3006A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325469 | ||||||
| chr8:109325532
|
T | TA | 4 | a0006c0006t0008g0168a0006c0006t0008g0334a0006c0006t0008g0335others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-3070dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325532 | ||||||
| chr8:109325583
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.119-3120C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325583 | ||||||
| chr8:109325633
|
C | T | 5 | a0003c0003t0008g0030a0006c0006t0008g0168a0006c0006t0008g0334others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-3170G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325633 | ||||||
| chr8:109325729
|
T | C | 1 | a0003c0003t0006g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.119-3266A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325729 | ||||||
| chr8:109325951
|
G | C | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.119-3488C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109325951 | ||||||
| chr8:109326163
|
C | T | 1 | a0004c0004t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.119-3700G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326163 | ||||||
| chr8:109326408
|
G | C | 31 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0003g0175others(28): Show | 31 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.119-3945C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326408 | ||||||
| chr8:109326460
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.119-3997G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326460 | ||||||
| chr8:109326502
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.119-4039C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326502 | ||||||
| chr8:109326537
|
TGAA | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-4077_119-4075d others(5): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326537 | ||||||
| chr8:109326604
|
A | G | 2 | a0003c0003t0006g0009a0003c0003t0006g0212 | 3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.119-4141T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326604 | ||||||
| chr8:109326649
|
C | A | 3 | a0002c0002t0002g0293a0002c0002t0002g0294a0002c0002t0002g0295 | 3 | NA19009.hp1 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.119-4186G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326649 | ||||||
| chr8:109326680
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.119-4217C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326680 | ||||||
| chr8:109326799
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.119-4336A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326799 | ||||||
| chr8:109326886
|
T | C | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-4423A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326886 | ||||||
| chr8:109326966
|
T | C | 3 | a0002c0002t0002g0307a0002c0002t0002g0308a0002c0002t0002g0309 | 3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.119-4503A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109326966 | ||||||
| chr8:109327038
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.119-4575C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327038 | ||||||
| chr8:109327211
|
A | G | 1 | a0004c0004t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.119-4748T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327211 | ||||||
| chr8:109327220
|
G | A | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-4757C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327220 | ||||||
| chr8:109327470
|
A | G | 1 | a0002c0002t0002g0232 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.119-5007T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327470 | ||||||
| chr8:109327505
|
C | T | 4 | a0003c0003t0003g0035a0003c0003t0003g0036a0003c0003t0003g0037others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-5042G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327505 | ||||||
| chr8:109327602
|
T | A | 1 | a0002c0002t0002g0310 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.119-5139A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327602 | ||||||
| chr8:109327728
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.119-5265T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327728 | ||||||
| chr8:109327804
|
G | A | 1 | a0003c0003t0003g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119-5341C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327804 | ||||||
| chr8:109327898
|
G | C | 1 | a0002c0002t0002g0327 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.119-5435C>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109327898 | ||||||
| chr8:109328146
|
C | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-5683G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328146 | ||||||
| chr8:109328150
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.119-5687A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328150 | ||||||
| chr8:109328170
|
A | G | 9 | a0005c0005t0007g0171a0005c0005t0007g0172a0005c0005t0007g0173others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-5707T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328170 | ||||||
| chr8:109328254
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.118+5639C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328254 | ||||||
| chr8:109328353
|
C | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+5540G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328353 | ||||||
| chr8:109328487
|
A | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118+5406T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328487 | ||||||
| chr8:109328776
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.118+5117T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328776 | ||||||
| chr8:109328911
|
T | C | 2 | a0005c0005t0007g0207a0005c0005t0007g0208 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.118+4982A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328911 | ||||||
| chr8:109328947
|
G | A | 1 | a0002c0002t0014g0220 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.118+4946C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328947 | ||||||
| chr8:109328970
|
A | T | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118+4923T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109328970 | ||||||
| chr8:109329039
|
G | A | 1 | a0003c0003t0003g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.118+4854C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109329039 | ||||||
| chr8:109329547
|
C | T | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+4346G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109329547 | ||||||
| chr8:109329589
|
C | T | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+4304G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109329589 | ||||||
| chr8:109329742
|
T | G | 1 | a0002c0002t0002g0311 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.118+4151A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109329742 | ||||||
| chr8:109329800
|
C | T | 5 | a0003c0003t0004g0041a0003c0003t0004g0044a0003c0003t0004g0045others(2): Show | 5 | HG01934.hp1 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+4093G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109329800 | ||||||
| chr8:109330000
|
C | T | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3893G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330000 | ||||||
| chr8:109330069
|
GAAACATA others(3): Show |
G | 1 | a0002c0002t0002g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.118+3814_118+3823d others(12): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330069 | ||||||
| chr8:109330199
|
T | A | 1 | a0003c0003t0003g0199 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.118+3694A>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330199 | ||||||
| chr8:109330311
|
A | G | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.118+3582T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330311 | ||||||
| chr8:109330571
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.118+3322T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330571 | ||||||
| chr8:109330617
|
A | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.118+3276T>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330617 | ||||||
| chr8:109330671
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.118+3222T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330671 | ||||||
| chr8:109330686
|
G | A | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.118+3207C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330686 | ||||||
| chr8:109330718
|
C | A | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+3175G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109330718 | ||||||
| chr8:109331080
|
G | A | 1 | a0002c0002t0002g0312 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.118+2813C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331080 | ||||||
| chr8:109331108
|
C | T | 1 | a0002c0002t0002g0318 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.118+2785G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331108 | ||||||
| chr8:109331138
|
C | T | 1 | a0003c0003t0013g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+2755G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331138 | ||||||
| chr8:109331158
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.118+2735A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331158 | ||||||
| chr8:109331266
|
G | A | 16 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(13): Show | 17 | HG01167.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+2627C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331266 | ||||||
| chr8:109331369
|
A | G | 3 | a0007c0007t0001g0055a0007c0007t0001g0057a0007c0007t0017g0056 | 3 | HG03017.hp2 HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.118+2524T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331369 | ||||||
| chr8:109331383
|
G | A | 1 | a0003c0003t0003g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+2510C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331383 | ||||||
| chr8:109331388
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.118+2505G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331388 | ||||||
| chr8:109331407
|
T | G | 1 | a0003c0003t0003g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.118+2486A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331407 | ||||||
| chr8:109331449
|
G | T | 3 | a0002c0002t0002g0228a0002c0002t0002g0229a0002c0002t0016g0230 | 3 | HG00735.hp1 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.118+2444C>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331449 | ||||||
| chr8:109331515
|
C | CA | 28 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(25): Show | 29 | HG00140.hp1 HG00280.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.118+2377dupT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331515 | ||||||
| chr8:109331515
|
CA | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 67 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(64): Show |
intron_variant | MODIFIER | c.118+2377delT | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331515 | ||||||
| chr8:109331515
|
CAA | C | 10 | a0003c0003t0003g0169a0003c0003t0003g0170a0003c0003t0004g0041others(7): Show | 10 | HG01109.hp1 HG01167.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+2376_118+2377d others(4): Show |
NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331515 | ||||||
| chr8:109331540
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.118+2353G>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331540 | ||||||
| chr8:109331557
|
T | C | 10 | a0002c0002t0002g0318a0002c0002t0002g0319a0002c0002t0002g0320others(7): Show | 10 | HG00558.hp1 HG02129.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+2336A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331557 | ||||||
| chr8:109331563
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.118+2330C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331563 | ||||||
| chr8:109331620
|
A | G | 1 | a0006c0006t0008g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.118+2273T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331620 | ||||||
| chr8:109331625
|
G | A | 3 | a0003c0003t0008g0032a0003c0003t0008g0033a0003c0011t0008g0031 | 3 | HG02257.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.118+2268C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331625 | ||||||
| chr8:109331868
|
G | A | 1 | a0002c0002t0002g0328 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118+2025C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109331868 | ||||||
| chr8:109332367
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.118+1526T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332367 | ||||||
| chr8:109332370
|
A | C | 33 | a0002c0002t0008g0333a0003c0003t0004g0015a0003c0003t0004g0041others(30): Show | 35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.118+1523T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332370 | ||||||
| chr8:109332378
|
A | G | 11 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(8): Show | 12 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+1515T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332378 | ||||||
| chr8:109332453
|
A | G | 1 | a0002c0002t0014g0220 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.118+1440T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332453 | ||||||
| chr8:109332536
|
A | G | 7 | a0003c0003t0003g0034a0003c0003t0003g0035a0003c0003t0003g0036others(4): Show | 7 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+1357T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332536 | ||||||
| chr8:109332827
|
A | C | 18 | a0003c0003t0005g0001a0003c0003t0005g0017a0003c0003t0005g0018others(15): Show | 19 | HG01109.hp1 HG01167.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.118+1066T>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332827 | ||||||
| chr8:109332909
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.118+984T>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332909 | ||||||
| chr8:109332955
|
T | C | 22 | a0001c0001t0001g0342a0002c0002t0008g0333a0003c0003t0004g0015others(19): Show | 24 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+938A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109332955 | ||||||
| chr8:109333009
|
T | C | 1 | a0002c0002t0002g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.118+884A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333009 | ||||||
| chr8:109333032
|
C | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.118+861G>A | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333032 | ||||||
| chr8:109333153
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.118+740A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333153 | ||||||
| chr8:109333188
|
T | G | 1 | a0002c0002t0002g0331 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.118+705A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333188 | ||||||
| chr8:109333213
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118+680A>G | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333213 | ||||||
| chr8:109333373
|
G | A | 13 | a0001c0001t0001g0332a0001c0001t0001g0342a0002c0002t0008g0333others(10): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.118+520C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333373 | ||||||
| chr8:109333433
|
G | A | 1 | a0003c0003t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.118+460C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333433 | ||||||
| chr8:109333659
|
G | A | 1 | a0003c0003t0004g0344 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118+234C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333659 | ||||||
| chr8:109333674
|
G | A | 1 | a0003c0003t0004g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118+219C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333674 |