Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0002 | 1/1 | 583 | 118 | 7 | 23 | 70 | 3 | 13 | 51 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0003 | 0/0 | 583 | 83 | 52 | 13 | 9 | 2 | 7 | 7 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0004 | 0/0 | 583 | 14 | 0 | 1 | 0 | 2 | 11 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0005 | 0/0 | 583 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0006 | 0/0 | 583 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0007 | 0/0 | 583 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0008 | 0/0 | 583 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| a0009 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | MEVAA others(578): Show |
chr8 | 109235919 | 109339087 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1749 | 126 | 17 | 27 | 69 | 7 | 6 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0002c0002 | 1/1 | 1749 | 117 | 7 | 23 | 69 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0002c0010 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0003c0003 | 0/0 | 1749 | 82 | 51 | 13 | 9 | 2 | 7 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0003c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0004c0004 | 0/0 | 1749 | 14 | 0 | 1 | 0 | 2 | 11 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0005c0005 | 0/0 | 1749 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0006c0006 | 0/0 | 1749 | 4 | 4 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0007c0007 | 0/0 | 1749 | 3 | 0 | 0 | 0 | 0 | 3 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0008c0008 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
chr8 | 109235919 | 109339087 | ||
| a0009c0009 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | ATGGA others(1744): Show |
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 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0001c0001t0010 | 0/0 | 3922 | 3 | 0 | 1 | 0 | 1 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0001c0001t0018 | 0/0 | 3922 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0001c0001t0019 | 0/0 | 3922 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0002 | 1/1 | 3919 | 111 | 6 | 20 | 67 | 3 | 13 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0008 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0011 | 0/0 | 3919 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0014 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0015 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0002c0002t0016 | 0/0 | 3919 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0002c0010t0002 | 0/0 | 3919 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3914): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0003 | 0/0 | 3923 | 36 | 12 | 8 | 9 | 2 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0004 | 0/0 | 3923 | 21 | 16 | 3 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0005 | 0/0 | 3923 | 12 | 11 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0006 | 0/0 | 3924 | 9 | 8 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3919): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0008 | 0/0 | 3923 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0003c0003t0013 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0003c0011t0008 | 0/0 | 3923 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0004c0004t0001 | 0/0 | 3922 | 8 | 0 | 1 | 0 | 1 | 6 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0004c0004t0009 | 0/0 | 3922 | 6 | 0 | 0 | 0 | 1 | 5 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0005c0005t0007 | 0/0 | 3924 | 9 | 9 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3919): Show |
chr8 | 109235919 | 109339087 |
| a0006c0006t0008 | 0/0 | 3923 | 4 | 4 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0007c0007t0001 | 0/0 | 3922 | 2 | 0 | 0 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0007c0007t0017 | 0/0 | 3922 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3917): Show |
chr8 | 109235919 | 109339087 |
| a0008c0008t0003 | 0/0 | 3923 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3918): Show |
chr8 | 109235919 | 109339087 |
| a0009c0009t0012 | 0/0 | 3920 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | AGTCT others(3915): Show |
chr8 | 109235919 | 109339087 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| 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 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0010g0011 | 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 |
| a0001c0001t0018g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0001c0001t0019g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0011g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0014g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0015g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0002t0016g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0002c0010t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0003c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 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 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 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 |
| a0003c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0003t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0003c0011t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0004c0004t0009g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0005c0005t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0005c0005t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0005c0005t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0006c0006t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0007c0007t0017g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0008c0008t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0008c0008t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| a0009c0009t0012g0055 | 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 | g0065 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0256 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00140 | hp2 | a0004 | c0004 | t0001 | g0139 | EUR | GBR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00280 | hp1 | a0004 | c0004 | t0009 | g0162 | EUR | FIN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00558 | hp2 | a0002 | c0002 | t0011 | g0016 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00621 | hp2 | a0001 | c0001 | t0018 | g0078 | EAS | CHS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00639 | hp1 | a0003 | c0003 | t0003 | g0188 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00741 | hp1 | a0003 | c0003 | t0003 | g0045 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG00741 | hp2 | a0003 | c0003 | t0003 | g0206 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0252 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01099 | hp1 | a0002 | c0002 | t0016 | g0227 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0157 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01109 | hp1 | a0003 | c0003 | t0006 | g0034 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0235 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01167 | hp1 | a0003 | c0003 | t0005 | g0030 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0166 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01168 | hp1 | a0003 | c0003 | t0003 | g0182 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0213 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01243 | hp2 | a0002 | c0002 | t0015 | g0291 | AMR | PUR | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0295 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01257 | hp1 | a0002 | c0002 | t0014 | g0217 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0293 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0292 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0181 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0226 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01516 | hp2 | a0003 | c0003 | t0003 | g0167 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0184 | EUR | IBS | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0015 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01884 | hp2 | a0006 | c0006 | t0008 | g0325 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01891 | hp1 | a0005 | c0005 | t0007 | g0204 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01891 | hp2 | a0006 | c0006 | t0008 | g0324 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01934 | hp1 | a0003 | c0003 | t0004 | g0054 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0287 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0186 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0318 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0322 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0174 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02145 | hp1 | a0003 | c0003 | t0004 | g0330 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02145 | hp2 | a0005 | c0005 | t0007 | g0168 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | CDX | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02257 | hp1 | a0009 | c0009 | t0012 | g0055 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02257 | hp2 | a0003 | c0011 | t0008 | g0038 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02258 | hp2 | a0003 | c0003 | t0005 | g0005 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0192 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02280 | hp2 | a0005 | c0005 | t0007 | g0198 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02293 | hp1 | a0003 | c0003 | t0004 | g0052 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0218 | EAS | KHV | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0043 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02615 | hp2 | a0003 | c0003 | t0005 | g0005 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02622 | hp2 | a0003 | c0003 | t0004 | g0334 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02630 | hp2 | a0003 | c0003 | t0006 | g0035 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0047 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02647 | hp2 | a0005 | c0005 | t0007 | g0169 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02683 | hp1 | a0004 | c0004 | t0009 | g0163 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02683 | hp2 | a0003 | c0003 | t0004 | g0053 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02698 | hp1 | a0003 | c0003 | t0003 | g0183 | 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 | g0209 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0041 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0296 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02738 | hp1 | a0004 | c0004 | t0001 | g0158 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0246 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02809 | hp2 | a0003 | c0003 | t0004 | g0211 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02818 | hp1 | a0003 | c0003 | t0005 | g0025 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02818 | hp2 | a0005 | c0005 | t0007 | g0170 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02886 | hp1 | a0003 | c0003 | t0004 | g0216 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0190 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02896 | hp2 | a0003 | c0003 | t0008 | g0039 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02897 | hp1 | a0003 | c0003 | t0008 | g0040 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02897 | hp2 | a0003 | c0003 | t0004 | g0215 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02965 | hp1 | a0003 | c0003 | t0013 | g0036 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02965 | hp2 | a0003 | c0003 | t0003 | g0044 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02970 | hp1 | a0006 | c0006 | t0008 | g0165 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0329 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02976 | hp1 | a0003 | c0003 | t0006 | g0033 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02976 | hp2 | a0003 | c0003 | t0004 | g0022 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03017 | hp1 | a0004 | c0004 | t0001 | g0159 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03017 | hp2 | a0007 | c0007 | t0017 | g0063 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0029 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03041 | hp2 | a0003 | c0003 | t0006 | g0332 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03098 | hp1 | a0008 | c0008 | t0003 | g0179 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03098 | hp2 | a0003 | c0003 | t0006 | g0015 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0244 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0189 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03195 | hp1 | a0003 | c0003 | t0004 | g0022 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03195 | hp2 | a0003 | c0003 | t0003 | g0046 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03209 | hp1 | a0003 | c0003 | t0005 | g0031 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03209 | hp2 | a0003 | c0003 | t0004 | g0214 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03225 | hp2 | a0005 | c0005 | t0007 | g0205 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03239 | hp1 | a0004 | c0004 | t0009 | g0161 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03239 | hp2 | a0007 | c0007 | t0001 | g0064 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03453 | hp1 | a0003 | c0003 | t0004 | g0210 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03453 | hp2 | a0005 | c0005 | t0007 | g0171 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03486 | hp1 | a0003 | c0003 | t0005 | g0032 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03486 | hp2 | a0003 | c0003 | t0006 | g0050 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0193 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03490 | hp2 | a0004 | c0004 | t0009 | g0014 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0138 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0297 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03492 | hp2 | a0004 | c0004 | t0009 | g0014 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03516 | hp1 | a0003 | c0003 | t0006 | g0049 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03516 | hp2 | a0006 | c0006 | t0008 | g0323 | AFR | ESN | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03540 | hp1 | a0008 | c0008 | t0003 | g0194 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0328 | AFR | GWD | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03579 | hp2 | a0003 | c0003 | t0004 | g0327 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0273 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03688 | hp2 | a0003 | c0003 | t0003 | g0172 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03710 | hp1 | a0007 | c0007 | t0001 | g0062 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0277 | SAS | PJL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03831 | hp1 | a0003 | c0003 | t0004 | g0051 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03831 | hp2 | a0004 | c0004 | t0001 | g0150 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03927 | hp1 | a0004 | c0004 | t0001 | g0067 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0202 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0301 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0245 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0274 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04199 | hp1 | a0004 | c0004 | t0009 | g0160 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04204 | hp1 | a0004 | c0004 | t0001 | g0137 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | STU | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18522 | hp1 | a0003 | c0003 | t0005 | g0208 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18747 | hp2 | a0002 | c0010 | t0002 | g0280 | EAS | CHB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18906 | hp2 | a0003 | c0003 | t0004 | g0048 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18944 | hp1 | a0001 | c0001 | t0019 | g0088 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0173 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18970 | hp2 | a0003 | c0003 | t0003 | g0175 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0314 | 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 | g0312 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18981 | hp1 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18985 | hp2 | a0003 | c0003 | t0003 | g0203 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0176 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0196 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0180 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0333 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19043 | hp1 | a0003 | c0003 | t0008 | g0037 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19043 | hp2 | a0003 | c0003 | t0003 | g0042 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19057 | hp2 | a0003 | c0003 | t0003 | g0177 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19065 | hp1 | a0002 | c0002 | t0011 | g0016 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | 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 | g0106 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0197 | AFR | YRI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20129 | hp2 | a0003 | c0003 | t0005 | g0026 | AFR | ASW | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0011 | EUR | TSI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0237 | EUR | TSI | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0191 | SAS | GIH | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0236 | SAS | GIH | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01123 | hp1 | a0003 | c0003 | t0003 | g0185 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | CLM | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02109 | hp1 | a0003 | c0003 | t0005 | g0028 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02109 | hp2 | a0005 | c0005 | t0007 | g0199 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0263 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG02559 | hp2 | a0005 | c0005 | t0007 | g0200 | AFR | ACB | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03471 | hp1 | a0003 | c0003 | t0005 | g0027 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG03471 | hp2 | a0003 | c0003 | t0004 | g0212 | AFR | MSL | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG06807 | hp1 | a0003 | c0003 | t0004 | g0326 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| HG06807 | hp2 | a0003 | c0003 | t0003 | g0187 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0195 | AFR | USA | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| NA21309 | hp2 | a0003 | c0003 | t0005 | g0024 | AFR | LWK | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0300 | REF | REF | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0261 | REF | REF | NUDCD1_chr8_109235919_109339087 | NUDCD1 | chr8 | 109235919 | 109339087 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001 a0004 a0007 |
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 | a0001 a0003 a0004 others(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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109241012 | C | T | 3 | a0003c0003t0004 a0003c0003t0006 a0009c0009t0012 |
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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(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 | a0003c0003t0003 a0008c0008t0003 |
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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(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 | a0003c0003t0006 a0005c0005t0007 a0009c0009t0012 |
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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0018 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:109243367 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0214 | 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 | a0002c0002t0002g0229 a0002c0002t0002g0259 a0002c0002t0002g0264 others(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 | a0002c0002t0002g0202 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0003c0003t0003g0185 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(181): 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 | a0003c0003t0004g0330 | 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | a0003c0003t0004g0048 | 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 | a0001c0001t0001g0145 | 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 | a0003c0003t0004g0022 a0003c0003t0004g0210 a0003c0003t0004g0211 others(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 | a0001c0001t0001g0127 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0093 | 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 | a0002c0002t0002g0225 | 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 | a0003c0003t0004g0216 a0003c0003t0004g0330 |
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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0299 | 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 | a0003c0003t0004g0022 a0003c0003t0004g0329 |
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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0004g0022 a0003c0003t0004g0328 a0003c0003t0004g0329 others(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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0005c0005t0007g0170 a0005c0005t0007g0198 a0005c0005t0007g0199 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0001c0001t0001g0066 | 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 | a0002c0002t0002g0202 a0002c0002t0002g0207 a0002c0002t0002g0231 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0003g0183 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0001c0001t0001g0082 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0002c0002t0002g0270 | 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 | a0002c0002t0002g0270 | 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 | a0002c0002t0002g0270 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0140 others(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 | a0002c0002t0008g0322 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0331 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0001c0001t0001g0112 | 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 | a0003c0003t0004g0214 | 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 | a0002c0002t0002g0270 | 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 | a0001c0001t0001g0079 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0004c0004t0001g0137 | 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 | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(188): 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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): 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 | a0001c0001t0001g0128 a0002c0002t0002g0225 a0002c0002t0002g0226 others(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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): 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 | 5 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0097 others(2): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0004g0334 | 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 | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(188): 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 | a0004c0004t0001g0067 a0004c0004t0001g0138 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0006g0332 | 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 | 39 | a0002c0002t0002g0004 a0002c0002t0002g0018 a0002c0002t0002g0202 others(36): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0092 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0003c0003t0008g0037 a0005c0005t0007g0168 a0005c0005t0007g0169 others(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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0122 others(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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(121): 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0122 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0004g0210 a0003c0003t0004g0211 a0003c0003t0004g0212 others(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 | a0003c0003t0003g0173 a0003c0003t0003g0174 |
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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0003c0003t0006g0332 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0262 | 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 | a0002c0002t0002g0262 | 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 | a0002c0002t0002g0248 a0002c0002t0002g0270 |
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 | a0002c0002t0002g0229 | 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 | a0005c0005t0007g0171 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0104 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0287 others(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 | a0003c0003t0008g0039 a0003c0003t0008g0040 |
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 | a0001c0001t0001g0095 | 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 | a0002c0002t0002g0270 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0331 | 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 | a0002c0002t0002g0270 | 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 | a0002c0002t0002g0308 a0002c0002t0002g0309 a0002c0002t0002g0310 |
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 | a0006c0006t0008g0325 | 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 | a0002c0002t0002g0232 a0002c0002t0002g0233 a0002c0002t0011g0016 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0255 | 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 | a0001c0001t0001g0164 | 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(191): 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0092 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0105 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0003c0003t0003g0041 | 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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0002c0002t0002g0246 | 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 | a0004c0004t0001g0159 | 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 | a0001c0001t0001g0129 | 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 | a0004c0004t0001g0159 | 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 | a0003c0003t0013g0036 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0006g0015 a0003c0003t0006g0033 a0003c0003t0006g0034 others(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 | a0002c0002t0002g0268 a0002c0002t0002g0269 |
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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0171 |
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 | a0003c0003t0004g0334 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0045 |
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 | a0001c0001t0001g0331 | 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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): 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 | a0003c0003t0004g0022 a0003c0003t0004g0327 a0003c0003t0004g0328 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0004c0004t0001g0139 | 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 | a0001c0001t0001g0331 | 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 | a0002c0002t0002g0297 a0002c0002t0002g0298 |
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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0003c0003t0013g0036 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0148 | 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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0001c0001t0001g0331 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0003g0166 | 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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0066 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0004c0004t0001g0150 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0002c0002t0002g0303 | 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 | a0003c0003t0004g0334 | 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 | a0003c0003t0003g0046 | 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 | a0002c0002t0002g0235 | 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 | a0002c0002t0002g0310 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(173): 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 | a0003c0003t0008g0037 | 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 | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0058 others(10): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0123 others(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 | a0002c0002t0002g0240 a0002c0002t0002g0273 |
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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0003g0043 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0004c0004t0001g0157 | 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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(241): 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 | a0002c0002t0002g0308 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0117 |
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 | a0003c0003t0008g0037 | 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 | a0002c0002t0002g0289 | 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 | 52 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0021 others(49): 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 | a0002c0002t0002g0258 a0002c0002t0002g0288 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0331 a0003c0003t0003g0173 a0003c0003t0003g0174 others(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 | a0003c0003t0003g0196 a0003c0003t0005g0026 a0003c0003t0005g0027 others(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 | 27 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(24): 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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(38): 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 |
42 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0057 others(39): 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 |
22 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0068 others(19): 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0129 |
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 | a0002c0002t0002g0286 | 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 | a0004c0004t0001g0150 | 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 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0305 |
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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0225 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0003c0003t0006g0332 | 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 | a0002c0002t0008g0322 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0260 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0004g0216 a0003c0003t0004g0330 |
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 | 1 | a0001c0001t0001g0007 | 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 | a0002c0002t0002g0287 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0232 | 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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0001c0001t0001g0144 | 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0005c0005t0007g0204 | 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | 2 | a0001c0001t0001g0013 a0001c0001t0001g0125 |
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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0164 | 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 | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(219): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0238 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0018 a0002c0002t0002g0202 a0002c0002t0002g0225 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0045 a0003c0003t0003g0046 others(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 | a0002c0002t0002g0309 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0084 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0090 a0001c0001t0001g0221 a0001c0001t0019g0088 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0001c0001t0001g0135 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0003c0003t0003g0042 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0003c0003t0004g0048 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0225 a0002c0002t0002g0226 a0002c0002t0016g0227 |
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 | a0003c0003t0004g0216 a0003c0003t0004g0330 |
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 | a0002c0002t0002g0296 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0250 a0002c0002t0002g0251 a0002c0002t0002g0302 others(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 | a0003c0003t0006g0015 a0003c0003t0006g0209 a0003c0003t0006g0332 |
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 | a0002c0002t0008g0322 | 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 | a0001c0001t0001g0093 | 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 | a0003c0003t0003g0175 a0003c0003t0003g0176 a0003c0003t0003g0177 others(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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0001c0001t0001g0321 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0004c0004t0001g0157 | 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 | a0002c0002t0002g0308 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(208): 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 | a0003c0003t0003g0177 a0003c0003t0005g0005 a0003c0003t0005g0024 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | 1 | a0001c0001t0001g0007 | 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 | a0003c0003t0004g0327 | 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 | a0002c0002t0002g0245 | 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 | a0003c0003t0004g0022 a0003c0003t0004g0329 |
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 | 82 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1299+937delC | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270067 | |||||||
| chr8:109270067 | CGG | C | 30 | a0002c0002t0002g0020 a0002c0002t0002g0237 a0002c0002t0002g0243 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(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 | a0003c0003t0004g0333 | 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 | a0003c0003t0004g0328 | 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 | a0003c0003t0008g0037 | 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 | a0003c0003t0003g0176 a0003c0003t0003g0178 |
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 | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(326): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1299+920G>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270085 | |||||||
| chr8:109270088 | T | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(328): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1299+917A>C | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 8/9 | chr8 | 109270088 | |||||||
| chr8:109270089 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(326): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0003c0003t0003g0176 a0003c0003t0003g0178 |
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 | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(328): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): 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 | a0003c0003t0003g0176 a0003c0003t0003g0178 a0003c0003t0003g0203 |
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 | a0003c0003t0006g0049 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0268 a0002c0002t0002g0269 a0002c0002t0002g0303 |
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 | a0001c0001t0001g0126 | 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 | a0002c0002t0008g0322 | 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0006g0049 | 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 | a0003c0003t0013g0036 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0126 a0001c0001t0001g0127 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0245 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 39 | a0002c0002t0002g0225 a0002c0002t0002g0226 a0002c0002t0002g0240 others(36): Show |
40 | HG00735.hp1 HG00741.hp1 HG01099.hp1 others(37): 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0202 a0002c0002t0002g0207 a0002c0002t0002g0231 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0105 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(219): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0003c0003t0004g0334 | 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 | a0001c0001t0001g0023 a0002c0002t0002g0311 a0002c0002t0002g0312 |
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 | a0003c0003t0003g0173 a0003c0003t0003g0174 |
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 | a0003c0003t0004g0326 | 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 | a0005c0005t0007g0170 a0005c0005t0007g0198 a0005c0005t0007g0199 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0216 a0003c0003t0004g0330 |
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 | a0004c0004t0001g0158 | 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 | a0001c0001t0001g0331 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0002c0002t0002g0265 | 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 | a0002c0002t0002g0315 | 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 | 8 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): 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 | a0006c0006t0008g0323 | 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 | a0001c0001t0001g0136 | 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 | a0003c0011t0008g0038 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0006c0006t0008g0165 | 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 | a0002c0002t0002g0293 a0002c0002t0002g0294 a0002c0002t0002g0295 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0006c0006t0008g0165 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0279 | 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 | a0002c0002t0002g0226 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0002c0002t0002g0229 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0002c0002t0002g0230 a0002c0002t0002g0282 a0002c0002t0002g0283 others(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 | a0001c0001t0001g0147 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0006c0006t0008g0165 | 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 | a0002c0002t0002g0234 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0001c0001t0001g0082 | 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 | a0003c0003t0004g0214 | 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 | a0003c0003t0004g0329 | 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 | a0003c0003t0003g0167 a0003c0003t0003g0182 a0003c0003t0003g0183 others(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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0002c0002t0002g0242 a0002c0002t0002g0243 a0002c0002t0002g0244 others(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 | a0002c0002t0002g0303 | 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 | a0005c0005t0007g0170 a0005c0005t0007g0198 a0005c0005t0007g0199 others(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 | a0002c0002t0015g0291 | 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 | a0003c0003t0008g0037 | 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 | a0003c0003t0004g0210 a0003c0003t0004g0211 a0003c0003t0004g0212 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0003c0003t0003g0172 | 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 | 2 | a0001c0001t0001g0010 a0001c0001t0001g0056 |
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 | 1 | a0002c0002t0002g0017 | 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 | a0002c0002t0008g0322 a0006c0006t0008g0165 a0006c0006t0008g0323 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0331 | 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 | a0001c0001t0018g0078 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0058 others(10): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0334 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0003c0003t0004g0334 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0003c0003t0004g0210 a0003c0003t0004g0211 a0003c0003t0004g0212 others(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 | a0002c0002t0002g0299 | 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 | a0002c0002t0002g0293 a0002c0002t0002g0294 a0002c0002t0002g0295 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0003g0187 | 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 | a0003c0003t0003g0186 | 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 | a0002c0002t0002g0299 | 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 | a0001c0001t0001g0331 | 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 | a0003c0003t0004g0334 | 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 | a0001c0001t0001g0228 | 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 | a0003c0003t0003g0172 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0305 |
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 | a0003c0003t0013g0036 | 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 | a0002c0002t0002g0229 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0002c0002t0008g0322 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0112 a0003c0003t0003g0166 a0003c0003t0003g0191 others(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 | a0001c0001t0001g0082 a0002c0002t0002g0307 a0003c0003t0003g0203 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0053 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0264 a0002c0002t0002g0271 |
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 | a0002c0002t0002g0307 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0002c0002t0002g0268 a0002c0002t0002g0269 a0002c0002t0002g0275 others(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 | a0003c0003t0003g0166 a0003c0003t0003g0191 a0003c0003t0003g0193 |
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 | a0003c0003t0003g0180 | 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 | a0001c0001t0001g0331 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0301 a0003c0003t0003g0173 a0003c0003t0003g0176 others(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 | a0002c0002t0002g0252 a0002c0002t0002g0254 a0002c0002t0008g0322 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(141): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0026 others(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 | a0003c0003t0003g0166 a0003c0003t0003g0175 a0003c0003t0003g0177 others(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 | a0003c0003t0003g0167 a0003c0003t0003g0172 a0003c0003t0003g0173 others(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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0002c0002t0002g0253 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0122 others(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 | a0003c0003t0006g0049 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): 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 | a0003c0003t0003g0041 a0003c0003t0003g0045 |
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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0152 a0002c0002t0002g0242 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0003g0166 | 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 | a0002c0002t0015g0291 | 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 | a0001c0001t0001g0331 | 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0002c0002t0002g0252 | 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 | a0002c0002t0002g0282 a0002c0002t0002g0283 a0002c0002t0002g0284 |
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 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
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 | 5 | a0001c0001t0001g0007 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0002c0002t0002g0293 a0002c0002t0002g0294 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0331 a0003c0003t0003g0173 a0003c0003t0003g0174 others(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 | a0001c0001t0001g0131 | 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 | a0003c0003t0008g0037 | 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 | a0006c0006t0008g0165 | 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 | a0006c0006t0008g0165 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0006c0006t0008g0323 a0006c0006t0008g0324 a0006c0006t0008g0325 |
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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(241): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0002c0002t0002g0270 a0003c0003t0003g0166 a0003c0003t0003g0167 others(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 | a0001c0001t0001g0135 | 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 | a0008c0008t0003g0179 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0001c0001t0001g0081 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0002c0002t0002g0207 | 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 | a0002c0002t0002g0231 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0240 a0002c0002t0002g0273 |
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 | a0001c0001t0001g0110 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0002c0002t0002g0019 a0002c0002t0002g0242 a0002c0002t0002g0243 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0004g0216 | 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 | a0001c0001t0001g0095 | 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 | a0003c0003t0003g0188 | 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 | a0008c0008t0003g0179 a0008c0008t0003g0194 |
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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(219): 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 | a0002c0002t0002g0268 a0002c0002t0002g0269 |
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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | 23 | a0002c0002t0002g0020 a0002c0002t0002g0240 a0002c0002t0002g0246 others(20): 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 | a0002c0002t0015g0291 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0002c0002t0002g0316 | 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 | a0003c0003t0008g0037 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0092 others(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 | a0002c0002t0002g0264 | 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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0004c0004t0001g0067 | 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 | a0002c0002t0008g0322 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | |||||||
| chr8:109292434 | C | CAGAT | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): 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 | a0001c0001t0001g0102 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0003g0191 | 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0117 |
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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0006g0332 | 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 | a0001c0001t0001g0331 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): 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 | a0001c0001t0001g0145 | 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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): 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 | a0003c0003t0004g0022 a0003c0003t0004g0048 a0003c0003t0004g0051 others(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 | a0003c0003t0003g0046 | 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 | a0001c0001t0001g0141 | 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 | 38 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0056 others(35): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0117 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0006g0332 | 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 | a0002c0002t0002g0302 a0002c0002t0002g0320 |
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 | a0001c0001t0001g0058 | 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 | a0002c0002t0002g0265 a0002c0002t0002g0266 a0002c0002t0002g0308 others(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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0171 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0016g0227 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0334 | 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 | a0002c0002t0002g0224 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0005g0032 | 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 | a0002c0002t0015g0291 | 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 | a0003c0003t0013g0036 | 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 | a0001c0001t0001g0155 | 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 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0112 | 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0001c0001t0001g0331 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0068 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0216 others(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 | a0003c0003t0006g0035 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0123 |
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 | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0004g0022 a0003c0003t0004g0327 a0003c0003t0004g0328 others(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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0001c0001t0001g0080 | 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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): 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 | a0003c0003t0013g0036 | 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0003g0043 a0003c0003t0003g0044 a0003c0003t0003g0047 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0003g0167 a0003c0003t0003g0182 a0003c0003t0003g0183 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | 1 | a0002c0002t0002g0020 | 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 | a0001c0001t0001g0331 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0278 a0002c0002t0002g0304 |
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 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0001c0001t0001g0116 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0171 |
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 | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(225): 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 | a0001c0001t0001g0133 | 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 | a0002c0002t0008g0322 | 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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0001c0001t0001g0133 | 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 | a0003c0003t0008g0037 | 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 | a0002c0002t0002g0292 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0091 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0210 others(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 | a0003c0003t0003g0174 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0136 | 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 | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0203 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0013g0036 | 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 | a0002c0002t0002g0268 a0002c0002t0002g0269 |
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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0313 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0004g0330 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): 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 | a0003c0003t0006g0049 a0003c0003t0006g0050 |
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 | 1 | a0002c0002t0002g0017 | 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 | a0001c0001t0018g0078 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0003c0003t0003g0175 a0003c0003t0003g0176 a0003c0003t0003g0177 others(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 | a0002c0002t0002g0267 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): 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 | a0005c0005t0007g0198 | 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 | a0003c0003t0004g0334 | 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 | a0002c0002t0008g0322 | 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 | a0003c0003t0004g0334 | 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 | a0008c0008t0003g0179 a0008c0008t0003g0194 |
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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(220): 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 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0117 |
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 | a0003c0003t0006g0050 | 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 | a0004c0004t0001g0137 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0099 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0001c0001t0001g0099 | 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 | a0003c0003t0005g0024 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0099 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0308 a0002c0002t0002g0309 a0002c0002t0002g0310 |
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 | a0001c0001t0001g0331 | 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 | a0003c0003t0004g0326 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0118 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0239 | 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 | a0003c0003t0004g0334 | 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 | a0001c0001t0001g0219 | 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 | a0003c0003t0003g0046 | 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 | a0002c0002t0008g0322 a0003c0003t0003g0166 a0003c0003t0003g0167 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | a0002c0002t0002g0268 a0002c0002t0002g0269 a0002c0002t0002g0275 others(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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): 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 | a0003c0003t0003g0182 a0003c0003t0004g0216 a0003c0003t0004g0330 others(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 | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): 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 | a0004c0004t0001g0067 | 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 | a0001c0001t0001g0094 | 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 | a0008c0008t0003g0194 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0154 |
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 | a0003c0003t0003g0046 | 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 | a0002c0002t0002g0244 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): 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 | |||||||
| chr8:109310226 | A | C | 1 | a0002c0002t0002g0289 | 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 | a0001c0001t0001g0060 | 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 | a0003c0003t0003g0181 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): 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 | a0002c0002t0002g0225 a0002c0002t0002g0234 a0002c0002t0002g0242 others(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 | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): 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 | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(224): 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0122 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0148 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): 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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(158): 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 | a0003c0003t0008g0037 | 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 | a0002c0002t0002g0229 | 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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0047 | 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 | a0001c0001t0001g0155 | 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 | a0002c0002t0002g0289 | 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 | a0003c0003t0013g0036 | 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 | a0002c0002t0008g0322 a0003c0003t0003g0166 a0003c0003t0003g0167 others(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 | a0002c0002t0002g0241 a0002c0002t0002g0317 |
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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0004c0004t0009g0161 | 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 | a0005c0005t0007g0199 a0005c0005t0007g0200 |
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 | a0005c0005t0007g0171 | 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 | a0005c0005t0007g0170 | 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 | a0005c0005t0007g0168 | 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 | a0005c0005t0007g0204 a0005c0005t0007g0205 |
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 | a0005c0005t0007g0169 a0005c0005t0007g0198 |
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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0003g0167 a0003c0003t0003g0182 a0003c0003t0003g0183 others(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 | a0003c0003t0003g0187 a0003c0003t0003g0188 |
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 | a0003c0003t0003g0167 a0003c0003t0003g0182 a0003c0003t0003g0183 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0003g0180 | 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 | a0003c0003t0003g0189 | 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 | a0006c0006t0008g0165 | 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 | a0003c0003t0003g0190 a0003c0003t0003g0196 |
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 | a0003c0003t0003g0166 a0003c0003t0003g0173 a0003c0003t0003g0174 |
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 | a0003c0003t0003g0175 a0003c0003t0003g0176 a0003c0003t0003g0191 others(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 | a0003c0003t0003g0177 a0003c0003t0003g0178 a0003c0003t0003g0181 others(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 | a0008c0008t0003g0179 a0008c0008t0003g0194 |
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 | a0003c0003t0003g0195 | 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 | a0003c0003t0003g0203 | 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 | a0003c0003t0003g0172 | 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 |
106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(103): 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 | a0001c0001t0001g0072 a0001c0001t0001g0095 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0003c0003t0003g0042 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | a0003c0003t0006g0049 a0003c0003t0006g0332 a0009c0009t0012g0055 |
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 | a0003c0003t0003g0043 | 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 | a0001c0001t0001g0331 a0003c0003t0003g0044 a0003c0003t0003g0047 others(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 | a0003c0003t0004g0216 | 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 | a0003c0003t0004g0022 a0003c0003t0004g0328 |
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 | a0003c0003t0003g0218 | 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 | a0006c0006t0008g0323 a0006c0006t0008g0324 a0006c0006t0008g0325 |
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 | a0003c0003t0003g0046 | 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 | a0003c0003t0003g0041 | 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 | a0003c0003t0004g0329 | 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 | a0004c0004t0009g0160 a0004c0004t0009g0163 |
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 | a0004c0004t0001g0150 | 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 | a0003c0003t0004g0326 a0004c0004t0001g0137 |
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 | a0004c0004t0001g0138 a0004c0004t0001g0157 |
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 | a0002c0002t0008g0322 a0004c0004t0001g0067 |
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 | a0004c0004t0001g0139 | 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 | a0003c0003t0004g0334 a0004c0004t0009g0014 a0004c0004t0009g0161 |
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 | a0004c0004t0001g0158 a0004c0004t0001g0159 |
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 | a0004c0004t0009g0162 | 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 | a0003c0003t0004g0330 | 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 | a0003c0003t0004g0048 | 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 | a0003c0003t0004g0052 | 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 | a0003c0003t0004g0054 | 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 | a0003c0003t0004g0053 | 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 | a0003c0003t0004g0051 | 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 | a0003c0003t0004g0211 a0003c0003t0004g0212 |
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 | a0003c0003t0004g0215 a0003c0003t0006g0015 |
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 | a0003c0003t0004g0213 | 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 | a0003c0003t0006g0209 | 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 | a0003c0003t0004g0214 | 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 | a0003c0003t0004g0210 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0236 a0009c0009t0012g0055 |
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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0003c0003t0004g0329 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0331 | 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 | a0002c0002t0002g0235 a0002c0002t0002g0239 a0002c0002t0002g0271 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0075 a0001c0001t0001g0098 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): 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 | a0001c0001t0001g0056 | 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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): 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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0004c0004t0001g0157 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0004g0334 | 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 | a0002c0002t0008g0322 | 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 | a0004c0004t0001g0067 | 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 | a0002c0002t0002g0224 | 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 | a0002c0002t0002g0240 a0002c0002t0002g0273 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0122 | 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 | a0003c0003t0004g0048 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0002c0002t0002g0289 | 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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0002c0002t0002g0274 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0123 | 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 | a0002c0002t0002g0273 | 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 | a0001c0001t0001g0124 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(117): 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 | a0003c0003t0003g0197 | 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 | a0003c0003t0003g0197 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 2 | a0001c0001t0001g0013 a0001c0001t0001g0125 |
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 | a0002c0002t0002g0297 a0002c0002t0002g0298 |
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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): 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 | 5 | a0001c0001t0001g0007 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0002g0225 a0002c0002t0002g0226 a0002c0002t0016g0227 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0131 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0013g0036 | 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 | a0002c0002t0002g0239 | 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 | a0001c0001t0001g0331 | 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 | a0002c0002t0002g0274 | 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 | a0003c0003t0004g0051 a0003c0003t0004g0052 a0003c0003t0004g0053 others(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 | T | 1 | a0002c0002t0002g0238 | 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 | a0002c0002t0002g0275 a0002c0002t0002g0276 |
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 | a0006c0006t0008g0323 a0006c0006t0008g0324 a0006c0006t0008g0325 |
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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0132 |
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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(141): 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 | a0003c0003t0004g0210 a0003c0003t0004g0211 a0003c0003t0004g0212 others(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 | a0008c0008t0003g0179 | 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 | a0002c0002t0002g0293 | 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 | a0004c0004t0009g0163 | 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 | a0003c0003t0006g0035 | 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 | a0002c0002t0002g0289 | 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 | a0001c0001t0001g0228 | 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0003c0003t0013g0036 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): 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 | a0003c0003t0013g0036 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0006c0006t0008g0165 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0331 | 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 | a0004c0004t0001g0159 | 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 | a0003c0003t0004g0051 a0003c0003t0004g0053 |
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 | a0002c0002t0002g0201 a0002c0002t0002g0236 a0002c0002t0002g0237 |
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 | a0003c0003t0004g0210 a0003c0003t0004g0211 a0003c0003t0004g0212 others(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 | a0002c0002t0002g0277 | 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 | a0001c0001t0001g0071 | 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 | a0002c0002t0002g0289 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0023 | 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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(141): 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 | a0003c0003t0004g0054 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0013g0036 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0002c0002t0002g0232 a0002c0002t0002g0234 a0002c0002t0002g0235 others(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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(161): 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0006c0006t0008g0325 | 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 | a0003c0003t0004g0330 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): 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 | a0002c0002t0002g0286 | 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 | a0001c0001t0001g0133 | 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 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0305 |
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 | a0002c0002t0002g0232 a0002c0002t0002g0233 a0002c0002t0002g0278 others(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 | a0003c0003t0013g0036 | 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 | a0001c0001t0001g0134 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(227): 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 | a0002c0002t0002g0290 | 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 | a0004c0004t0009g0014 a0004c0004t0009g0160 a0004c0004t0009g0161 others(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 | a0003c0003t0004g0334 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0005c0005t0007g0200 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0135 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0003c0003t0003g0173 a0003c0003t0003g0174 a0003c0003t0003g0175 others(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 | 3 | a0002c0002t0002g0021 a0002c0002t0002g0279 a0002c0010t0002g0280 |
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 | a0003c0003t0004g0051 a0003c0003t0004g0052 a0003c0003t0004g0053 others(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 | a0003c0003t0006g0015 | 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 | a0001c0001t0001g0069 | 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 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0002c0002t0002g0231 | 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 | a0002c0002t0002g0231 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0003g0172 | 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 | a0004c0004t0009g0014 a0004c0004t0009g0160 a0004c0004t0009g0161 others(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 | a0003c0003t0003g0206 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0004c0004t0001g0150 | 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 | a0001c0001t0001g0136 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0331 | 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0216 others(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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0003c0003t0008g0037 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0004g0051 a0003c0003t0004g0052 a0003c0003t0004g0053 others(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 | a0001c0001t0001g0331 | 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 | a0003c0003t0003g0042 a0003c0003t0003g0043 a0003c0003t0003g0044 others(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 | a0001c0001t0001g0319 | 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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0004g0334 a0005c0005t0007g0168 a0005c0005t0007g0169 others(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 | a0003c0003t0006g0015 a0003c0003t0006g0209 |
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 | a0004c0004t0001g0067 a0004c0004t0001g0137 a0004c0004t0001g0138 others(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 | a0001c0001t0001g0140 a0003c0003t0008g0039 a0003c0003t0008g0040 others(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 | a0001c0001t0001g0331 a0002c0002t0002g0232 a0002c0002t0002g0233 others(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 | a0007c0007t0001g0062 | 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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(228): 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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(228): 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 | a0002c0002t0002g0281 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0003c0003t0006g0049 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | a0001c0001t0001g0068 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0285 a0002c0002t0002g0286 a0002c0002t0002g0287 others(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 | a0003c0003t0006g0033 a0003c0003t0006g0034 a0003c0003t0006g0035 others(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 | a0006c0006t0008g0165 a0006c0006t0008g0323 a0006c0006t0008g0324 others(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 | a0001c0001t0001g0145 | 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 | a0003c0003t0008g0037 a0006c0006t0008g0165 a0006c0006t0008g0323 others(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 | a0003c0003t0006g0050 | 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 | a0003c0003t0004g0334 | 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 | a0004c0004t0001g0150 | 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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0003g0172 others(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 | a0002c0002t0002g0230 | 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 | a0001c0001t0001g0146 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0006g0015 a0003c0003t0006g0209 |
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 | a0002c0002t0002g0282 a0002c0002t0002g0283 a0002c0002t0002g0284 |
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 | a0001c0001t0001g0147 | 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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): 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 | a0003c0003t0013g0036 | 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 | a0002c0002t0002g0296 a0002c0002t0002g0297 a0002c0002t0002g0298 |
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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(241): 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 | a0004c0004t0001g0067 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0229 | 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 | a0003c0003t0003g0042 a0003c0003t0003g0043 a0003c0003t0003g0044 others(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 | a0002c0002t0002g0299 | 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 | a0001c0001t0001g0023 | 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 | a0003c0003t0003g0046 | 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 | a0002c0002t0002g0316 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0001c0001t0001g0148 | 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 | a0005c0005t0007g0168 a0005c0005t0007g0169 a0005c0005t0007g0170 others(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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(127): 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0008g0322 | 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 | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): 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 | a0005c0005t0007g0204 a0005c0005t0007g0205 |
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 | a0002c0002t0014g0217 | 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 | a0003c0003t0004g0334 | 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 | a0003c0003t0003g0206 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | |||||||
| chr8:109329800 | C | T | 5 | a0003c0003t0004g0048 a0003c0003t0004g0051 a0003c0003t0004g0052 others(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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0002c0002t0002g0225 | 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 | a0003c0003t0003g0196 | 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 | a0006c0006t0008g0165 | 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 | a0001c0001t0001g0066 | 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 | 1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0065 | 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 | a0006c0006t0008g0165 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0002g0301 | 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 | a0002c0002t0002g0307 | 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 | a0003c0003t0013g0036 | 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 | a0001c0001t0001g0149 | 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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0007c0007t0001g0062 a0007c0007t0001g0064 a0007c0007t0017g0063 |
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 | a0003c0003t0003g0197 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0003c0003t0003g0047 | 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 | a0002c0002t0002g0225 a0002c0002t0002g0226 a0002c0002t0016g0227 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0057 others(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 | a0003c0003t0003g0166 a0003c0003t0003g0167 a0003c0003t0004g0048 others(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 | a0001c0001t0001g0023 | 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 | a0002c0002t0002g0307 a0002c0002t0002g0308 a0002c0002t0002g0309 others(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 | a0001c0001t0001g0164 | 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 | a0006c0006t0008g0165 | 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 | a0003c0003t0008g0039 a0003c0003t0008g0040 a0003c0011t0008g0038 |
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 | a0002c0002t0002g0317 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): 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 | a0002c0002t0008g0322 a0003c0003t0004g0022 a0003c0003t0004g0048 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0002c0002t0014g0217 | 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 | a0003c0003t0003g0041 a0003c0003t0003g0042 a0003c0003t0003g0043 others(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 | a0003c0003t0005g0005 a0003c0003t0005g0024 a0003c0003t0005g0025 others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0331 a0002c0002t0008g0322 a0003c0003t0004g0022 others(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 | a0002c0002t0002g0318 | 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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(220): 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 | a0001c0001t0001g0319 | 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 | a0002c0002t0002g0320 | 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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0321 a0001c0001t0001g0331 a0002c0002t0008g0322 others(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 | a0003c0003t0006g0332 | 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 | a0003c0003t0004g0333 | 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 | a0003c0003t0004g0334 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118+219C>T | NUDCD1 | ENSG00000120526.12 | transcript | ENST00000239690.9 | protein_coding | 1/9 | chr8 | 109333674 |