Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23386 |
| ensemblid | ENSG00000015676.18 |
| hgncid | 22208 |
| symbol | NUDCD3 |
| name | NudC domain containing 3 |
| refseq_nuc | NM_015332.4 |
| refseq_prot | NP_056147.2 |
| ensembl_nuc | ENST00000355451.8 |
| ensembl_prot | ENSP00000347626.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 44379119 |
| end | 44490658 |
| strand | - |
| ver | v1.2 |
| region | chr7:44379119-44490658 |
| region5000 | chr7:44374119-44495658 |
| regionname0 | NUDCD3_chr7_44379119_44490658 |
| regionname5000 | NUDCD3_chr7_44374119_44495658 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 361 | 189 | 41 | 37 | 70 | 10 | 30 | 48 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | METGA others(356): Show |
chr7 | 44374119 | 44495658 |
| a0002 | 0/0 | 361 | 28 | 19 | 6 | 0 | 0 | 3 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | MEPGA others(356): Show |
chr7 | 44374119 | 44495658 |
| a0003 | 0/1 | 361 | 17 | 0 | 4 | 3 | 4 | 5 | 2 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | MEPGA others(356): Show |
chr7 | 44374119 | 44495658 |
| a0004 | 0/0 | 361 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | METGA others(356): Show |
chr7 | 44374119 | 44495658 |
| a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | METGV others(356): Show |
chr7 | 44374119 | 44495658 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1083 | 188 | 41 | 37 | 69 | 10 | 30 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0001c0006 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0002c0002 | 0/0 | 1083 | 26 | 17 | 6 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0002c0005 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0003c0003 | 0/1 | 1083 | 17 | 0 | 4 | 3 | 4 | 5 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0004c0004 | 0/0 | 1083 | 3 | 2 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 | ||
| a0005c0007 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | ATGGA others(1078): Show |
chr7 | 44374119 | 44495658 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8036 | 128 | 34 | 23 | 47 | 5 | 19 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0002 | 1/0 | 8036 | 25 | 0 | 4 | 9 | 4 | 7 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0003 | 0/0 | 8037 | 10 | 0 | 1 | 8 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0013 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0014 | 0/0 | 8037 | 2 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0015 | 0/0 | 8036 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0016 | 0/0 | 8036 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0017 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0024 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0025 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0026 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0027 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0028 | 0/0 | 8037 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0029 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0030 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0031 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0032 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0033 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0034 | 0/0 | 8037 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0035 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0036 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0037 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0001t0039 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0001c0006t0001 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0004 | 0/0 | 8036 | 8 | 1 | 4 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0007 | 0/0 | 8034 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8029): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0008 | 0/0 | 8034 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8029): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0010 | 0/0 | 8034 | 2 | 1 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8029): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0011 | 0/0 | 8034 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8029): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0018 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0020 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0021 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0022 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0023 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0038 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0002t0040 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0002c0005t0012 | 0/0 | 8037 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0003c0003t0005 | 0/0 | 8036 | 8 | 0 | 3 | 0 | 3 | 2 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0003c0003t0006 | 0/0 | 8036 | 4 | 0 | 0 | 3 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0003c0003t0009 | 0/1 | 8036 | 3 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0003c0003t0019 | 0/0 | 8036 | 2 | 0 | 0 | 0 | 1 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| a0004c0004t0003 | 0/0 | 8037 | 3 | 2 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8032): Show |
chr7 | 44374119 | 44495658 |
| a0005c0007t0001 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | AGTCG others(8031): Show |
chr7 | 44374119 | 44495658 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0014g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0014g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0015g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0016g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0017g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0024g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0025g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0026g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0028g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0029g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0030g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0031g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0032g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0033g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0034g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0035g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0036g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0037g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0001t0039g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0010g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0018g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0018g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0022g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0038g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0002t0040g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0005t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0002c0005t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0009g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0009g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0019g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0003c0003t0019g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0004c0004t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0004c0004t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0004c0004t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| a0005c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00099 | hp2 | a0003 | c0003 | t0005 | g0221 | EUR | GBR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00280 | hp1 | a0003 | c0003 | t0005 | g0233 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00280 | hp2 | a0003 | c0003 | t0019 | g0230 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0135 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00438 | hp1 | a0003 | c0003 | t0006 | g0234 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00609 | hp2 | a0005 | c0007 | t0001 | g0192 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00639 | hp1 | a0004 | c0004 | t0003 | g0024 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00642 | hp1 | a0001 | c0001 | t0016 | g0002 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00735 | hp2 | a0002 | c0002 | t0004 | g0212 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG00741 | hp2 | a0002 | c0002 | t0010 | g0193 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01070 | hp2 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01071 | hp1 | a0002 | c0002 | t0004 | g0213 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0210 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01109 | hp1 | a0001 | c0001 | t0032 | g0138 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01109 | hp2 | a0002 | c0002 | t0022 | g0215 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01168 | hp2 | a0003 | c0003 | t0005 | g0225 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01256 | hp1 | a0003 | c0003 | t0005 | g0222 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01257 | hp2 | a0001 | c0001 | t0015 | g0078 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01258 | hp1 | a0001 | c0001 | t0015 | g0052 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01258 | hp2 | a0003 | c0003 | t0005 | g0223 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01358 | hp2 | a0003 | c0003 | t0009 | g0228 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01496 | hp2 | a0001 | c0001 | t0030 | g0180 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0012 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01978 | hp2 | a0001 | c0001 | t0026 | g0186 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01981 | hp1 | a0001 | c0001 | t0031 | g0103 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02257 | hp1 | a0002 | c0002 | t0008 | g0204 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02280 | hp2 | a0002 | c0002 | t0038 | g0202 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02622 | hp1 | a0002 | c0002 | t0011 | g0194 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0071 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02683 | hp2 | a0002 | c0002 | t0004 | g0207 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02723 | hp2 | a0001 | c0001 | t0027 | g0146 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02738 | hp1 | a0003 | c0003 | t0019 | g0232 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0123 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02895 | hp1 | a0002 | c0002 | t0018 | g0199 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02922 | hp2 | a0002 | c0005 | t0012 | g0236 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0214 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03130 | hp1 | a0002 | c0002 | t0023 | g0209 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03139 | hp1 | a0002 | c0002 | t0010 | g0201 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0015 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03453 | hp1 | a0002 | c0002 | t0007 | g0197 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03453 | hp2 | a0001 | c0001 | t0033 | g0173 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03486 | hp1 | a0002 | c0002 | t0021 | g0217 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0067 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03491 | hp1 | a0003 | c0003 | t0005 | g0219 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03492 | hp2 | a0003 | c0003 | t0005 | g0218 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03516 | hp1 | a0002 | c0002 | t0007 | g0196 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03579 | hp1 | a0002 | c0005 | t0012 | g0235 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03831 | hp1 | a0001 | c0001 | t0024 | g0120 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03831 | hp2 | a0001 | c0001 | t0025 | g0129 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04184 | hp2 | a0003 | c0003 | t0009 | g0220 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04199 | hp2 | a0001 | c0001 | t0014 | g0009 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04204 | hp1 | a0003 | c0003 | t0006 | g0227 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0025 | AFR | YRI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0206 | AFR | YRI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18941 | hp1 | a0001 | c0001 | t0034 | g0028 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18965 | hp1 | a0001 | c0006 | t0001 | g0149 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18970 | hp1 | a0001 | c0001 | t0039 | g0091 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18979 | hp2 | a0003 | c0003 | t0006 | g0231 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18981 | hp1 | a0001 | c0001 | t0036 | g0144 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19005 | hp1 | a0001 | c0001 | t0035 | g0026 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19043 | hp1 | a0002 | c0002 | t0007 | g0198 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19063 | hp2 | a0001 | c0001 | t0028 | g0111 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19065 | hp2 | a0003 | c0003 | t0006 | g0229 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20805 | hp2 | a0003 | c0003 | t0005 | g0224 | EUR | TSI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20905 | hp2 | a0001 | c0001 | t0037 | g0080 | SAS | GIH | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0068 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02486 | hp2 | a0002 | c0002 | t0011 | g0195 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG02559 | hp2 | a0001 | c0001 | t0029 | g0054 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| HG06807 | hp2 | a0002 | c0002 | t0018 | g0200 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20300 | hp1 | a0002 | c0002 | t0020 | g0203 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA21309 | hp1 | a0002 | c0002 | t0040 | g0237 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| NA21309 | hp2 | a0002 | c0002 | t0008 | g0205 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0009 | g0226 | REF | REF | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44404523 | G | A | 1 | a0003 | 16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
missense_variant | MODERATE | c.703C>T | p.Arg235Cys | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/6 | 761/8036 | 703/1086 | 235/361 | chr7 | 44404523 | |||
| chr7:44485109 | T | A | 1 | a0004 | 3 | HG00639.hp1 HG03225.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.368A>T | p.Glu123Val | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 426/8036 | 368/1086 | 123/361 | chr7 | 44485109 | |||
| chr7:44485110 | C | T | 1 | a0004 | 3 | HG00639.hp1 HG03225.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.367G>A | p.Glu123Lys | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 425/8036 | 367/1086 | 123/361 | chr7 | 44485110 | |||
| chr7:44490587 | G | A | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.14C>T | p.Ala5Val | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 72/8036 | 14/1086 | 5/361 | chr7 | 44490587 | |||
| chr7:44490594 | T | G | 2 | a0002 a0003 |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
missense_variant | MODERATE | c.7A>C | p.Thr3Pro | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 65/8036 | 7/1086 | 3/361 | chr7 | 44490594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44392359 | A | G | 1 | a0001c0006 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.913T>C | p.Leu305Leu | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/6 | 971/8036 | 913/1086 | 305/361 | chr7 | 44392359 | |||
| chr7:44485075 | C | T | 1 | a0002c0005 | 2 | HG02922.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.402G>A | p.Gln134Gln | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 460/8036 | 402/1086 | 134/361 | chr7 | 44485075 | |||
| chr7:44490499 | G | A | 1 | a0002c0005 | 2 | HG02922.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.102C>T | p.Leu34Leu | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 160/8036 | 102/1086 | 34/361 | chr7 | 44490499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44379125 | T | A | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6886A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6886 | chr7 | 44379125 | ||||||
| chr7:44379147 | G | A | 1 | a0001c0001t0027 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6864C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6864 | chr7 | 44379147 | ||||||
| chr7:44379287 | C | CA | 3 | a0001c0001t0014 a0001c0001t0028 a0002c0005t0012 |
5 | HG01928.hp1 HG02922.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6723dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6723 | chr7 | 44379287 | ||||||
| chr7:44379293 | A | G | 1 | a0002c0002t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6718T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6718 | chr7 | 44379293 | ||||||
| chr7:44379382 | G | A | 1 | a0001c0001t0029 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6629C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6629 | chr7 | 44379382 | ||||||
| chr7:44379569 | A | G | 10 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 others(7): Show |
26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*6442T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6442 | chr7 | 44379569 | ||||||
| chr7:44379592 | C | T | 3 | a0003c0003t0005 a0003c0003t0006 a0003c0003t0019 |
14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6419G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6419 | chr7 | 44379592 | ||||||
| chr7:44379886 | G | A | 1 | a0001c0001t0034 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6125C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6125 | chr7 | 44379886 | ||||||
| chr7:44380008 | G | A | 1 | a0002c0002t0011 | 2 | HG02486.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6003C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6003 | chr7 | 44380008 | ||||||
| chr7:44380074 | T | A | 2 | a0002c0002t0004 a0002c0002t0022 |
9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5937A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5937 | chr7 | 44380074 | ||||||
| chr7:44380102 | C | T | 4 | a0002c0002t0004 a0002c0002t0020 a0002c0002t0022 others(1): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5909G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5909 | chr7 | 44380102 | ||||||
| chr7:44380129 | G | T | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5882C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5882 | chr7 | 44380129 | ||||||
| chr7:44380336 | G | C | 1 | a0002c0002t0007 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5675C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5675 | chr7 | 44380336 | ||||||
| chr7:44380548 | G | C | 8 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 others(5): Show |
23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5463C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5463 | chr7 | 44380548 | ||||||
| chr7:44380572 | G | A | 1 | a0003c0003t0019 | 2 | HG00280.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5439C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5439 | chr7 | 44380572 | ||||||
| chr7:44380573 | C | T | 2 | a0002c0002t0021 a0002c0002t0040 |
2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5438G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5438 | chr7 | 44380573 | ||||||
| chr7:44380639 | A | G | 8 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 others(5): Show |
23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5372T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5372 | chr7 | 44380639 | ||||||
| chr7:44380725 | G | A | 1 | a0001c0001t0030 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5286C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5286 | chr7 | 44380725 | ||||||
| chr7:44380763 | A | G | 5 | a0002c0002t0021 a0002c0002t0040 a0003c0003t0005 others(2): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5248T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5248 | chr7 | 44380763 | ||||||
| chr7:44380859 | A | C | 1 | a0002c0002t0022 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5152T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5152 | chr7 | 44380859 | ||||||
| chr7:44381040 | C | A | 3 | a0003c0003t0005 a0003c0003t0006 a0003c0003t0019 |
14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4971G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4971 | chr7 | 44381040 | ||||||
| chr7:44381051 | C | T | 2 | a0002c0002t0021 a0002c0002t0040 |
2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4960G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4960 | chr7 | 44381051 | ||||||
| chr7:44381052 | A | G | 3 | a0003c0003t0005 a0003c0003t0006 a0003c0003t0019 |
14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4959T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4959 | chr7 | 44381052 | ||||||
| chr7:44381155 | C | T | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(33): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*4856G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4856 | chr7 | 44381155 | ||||||
| chr7:44381302 | A | G | 2 | a0003c0003t0006 a0003c0003t0019 |
6 | HG00280.hp2 HG00438.hp1 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4709T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4709 | chr7 | 44381302 | ||||||
| chr7:44381489 | C | T | 1 | a0002c0005t0012 | 2 | HG02922.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4522G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4522 | chr7 | 44381489 | ||||||
| chr7:44381524 | T | C | 1 | a0001c0001t0031 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4487 | chr7 | 44381524 | ||||||
| chr7:44381793 | C | T | 1 | a0003c0003t0019 | 2 | HG00280.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4218G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4218 | chr7 | 44381793 | ||||||
| chr7:44381890 | C | G | 4 | a0003c0003t0005 a0003c0003t0006 a0003c0003t0009 others(1): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4121G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4121 | chr7 | 44381890 | ||||||
| chr7:44381984 | G | A | 1 | a0001c0001t0015 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4027C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4027 | chr7 | 44381984 | ||||||
| chr7:44382072 | T | C | 1 | a0001c0001t0032 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3939A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3939 | chr7 | 44382072 | ||||||
| chr7:44382131 | G | T | 1 | a0001c0001t0026 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3880C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3880 | chr7 | 44382131 | ||||||
| chr7:44382231 | A | C | 1 | a0001c0001t0025 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3780T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3780 | chr7 | 44382231 | ||||||
| chr7:44382239 | T | A | 1 | a0001c0001t0033 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3772A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3772 | chr7 | 44382239 | ||||||
| chr7:44382332 | A | G | 2 | a0002c0002t0021 a0002c0002t0040 |
2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3679T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3679 | chr7 | 44382332 | ||||||
| chr7:44382335 | G | GA | 3 | a0001c0001t0003 a0001c0001t0034 a0004c0004t0003 |
14 | HG00323.hp2 HG00639.hp1 HG02165.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3675dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3675 | chr7 | 44382335 | ||||||
| chr7:44382419 | C | T | 4 | a0002c0002t0004 a0002c0002t0020 a0002c0002t0022 others(1): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3592G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3592 | chr7 | 44382419 | ||||||
| chr7:44382475 | A | G | 6 | a0002c0002t0021 a0002c0002t0040 a0003c0003t0005 others(3): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3536T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3536 | chr7 | 44382475 | ||||||
| chr7:44382502 | G | A | 1 | a0001c0001t0016 | 2 | HG00642.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3509C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3509 | chr7 | 44382502 | ||||||
| chr7:44382518 | T | C | 1 | a0002c0002t0007 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3493A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3493 | chr7 | 44382518 | ||||||
| chr7:44382628 | C | T | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3383G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3383 | chr7 | 44382628 | ||||||
| chr7:44382650 | G | T | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3361C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3361 | chr7 | 44382650 | ||||||
| chr7:44382705 | G | A | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3306C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3306 | chr7 | 44382705 | ||||||
| chr7:44383164 | C | T | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2847G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2847 | chr7 | 44383164 | ||||||
| chr7:44383194 | G | A | 3 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2817 | chr7 | 44383194 | ||||||
| chr7:44383229 | G | C | 2 | a0001c0001t0013 a0001c0001t0017 |
4 | HG02109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2782 | chr7 | 44383229 | ||||||
| chr7:44383342 | T | G | 1 | a0001c0001t0035 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2669A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2669 | chr7 | 44383342 | ||||||
| chr7:44383378 | T | C | 1 | a0001c0001t0036 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2633A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2633 | chr7 | 44383378 | ||||||
| chr7:44383668 | G | A | 1 | a0002c0002t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2343C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2343 | chr7 | 44383668 | ||||||
| chr7:44383775 | C | T | 2 | a0002c0002t0021 a0002c0002t0040 |
2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2236G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2236 | chr7 | 44383775 | ||||||
| chr7:44383849 | G | A | 1 | a0002c0002t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2162C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2162 | chr7 | 44383849 | ||||||
| chr7:44383858 | C | T | 2 | a0001c0001t0024 a0002c0002t0010 |
3 | HG00741.hp2 HG03139.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2153G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2153 | chr7 | 44383858 | ||||||
| chr7:44383859 | G | A | 1 | a0001c0001t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2152 | chr7 | 44383859 | ||||||
| chr7:44383883 | C | T | 1 | a0002c0002t0010 | 2 | HG00741.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2128G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2128 | chr7 | 44383883 | ||||||
| chr7:44384195 | G | A | 1 | a0001c0001t0037 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1816C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1816 | chr7 | 44384195 | ||||||
| chr7:44384228 | C | G | 1 | a0001c0001t0013 | 2 | HG02622.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1783G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1783 | chr7 | 44384228 | ||||||
| chr7:44384459 | C | A | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1552G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1552 | chr7 | 44384459 | ||||||
| chr7:44384488 | CAT | C | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1521_*1522delAT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1521 | chr7 | 44384488 | ||||||
| chr7:44384612 | T | C | 17 | a0002c0002t0004 a0002c0002t0007 a0002c0002t0008 others(14): Show |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1399 | chr7 | 44384612 | ||||||
| chr7:44384654 | C | T | 15 | a0002c0002t0004 a0002c0002t0007 a0002c0002t0010 others(12): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1357 | chr7 | 44384654 | ||||||
| chr7:44385338 | G | A | 3 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*673C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 673 | chr7 | 44385338 | ||||||
| chr7:44385370 | T | C | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*641A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 641 | chr7 | 44385370 | ||||||
| chr7:44385384 | T | C | 4 | a0003c0003t0005 a0003c0003t0006 a0003c0003t0009 others(1): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*627A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 627 | chr7 | 44385384 | ||||||
| chr7:44385489 | CAA | C | 3 | a0002c0002t0007 a0002c0002t0010 a0002c0002t0011 |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521delTT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 520 | chr7 | 44385489 | ||||||
| chr7:44385626 | T | G | 2 | a0002c0002t0020 a0002c0002t0038 |
2 | HG02280.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 385 | chr7 | 44385626 | ||||||
| chr7:44385736 | T | C | 1 | a0001c0001t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 275 | chr7 | 44385736 | ||||||
| chr7:44385744 | C | T | 1 | a0002c0002t0020 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*267G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 267 | chr7 | 44385744 | ||||||
| chr7:44490636 | G | C | 1 | a0002c0002t0040 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 36 | chr7 | 44490636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44386355 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.976-234G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386355 | |||||||
| chr7:44386720 | C | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0001g0139 |
3 | HG02559.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.976-599G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386720 | |||||||
| chr7:44386757 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.976-636G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386757 | |||||||
| chr7:44386971 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.976-850G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386971 | |||||||
| chr7:44386989 | A | G | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.976-868T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386989 | |||||||
| chr7:44386997 | CAA | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0092 others(7): Show |
10 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-878_976-877del others(2): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386997 | |||||||
| chr7:44387019 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.976-898C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387019 | |||||||
| chr7:44387401 | T | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.976-1280A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387401 | |||||||
| chr7:44387550 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.976-1429C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387550 | |||||||
| chr7:44387693 | C | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.976-1572G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387693 | |||||||
| chr7:44387820 | G | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.976-1699C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387820 | |||||||
| chr7:44387900 | A | T | 31 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0040 others(28): Show |
31 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.976-1779T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387900 | |||||||
| chr7:44387993 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.976-1872C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387993 | |||||||
| chr7:44388046 | T | A | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.976-1925A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388046 | |||||||
| chr7:44388229 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.976-2108C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388229 | |||||||
| chr7:44388233 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.976-2112C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388233 | |||||||
| chr7:44388258 | C | T | 6 | a0001c0001t0001g0100 a0001c0001t0013g0071 a0001c0001t0013g0123 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2137G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388258 | |||||||
| chr7:44388259 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.976-2138C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388259 | |||||||
| chr7:44388435 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0056 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.976-2314T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388435 | |||||||
| chr7:44388514 | C | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0001g0139 |
3 | HG02559.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.976-2393G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388514 | |||||||
| chr7:44388514 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.976-2393G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388514 | |||||||
| chr7:44388881 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.976-2760A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388881 | |||||||
| chr7:44389076 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.976-2955A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389076 | |||||||
| chr7:44389261 | GAC | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.975+3034_975+3035d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389261 | |||||||
| chr7:44389282 | G | A | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+3015C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389282 | |||||||
| chr7:44389401 | G | A | 2 | a0003c0003t0006g0229 a0003c0003t0006g0231 |
2 | NA18979.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.975+2896C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389401 | |||||||
| chr7:44389507 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.975+2790A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389507 | |||||||
| chr7:44389691 | G | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.975+2606C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389691 | |||||||
| chr7:44389707 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.975+2590A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389707 | |||||||
| chr7:44389953 | T | C | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+2344A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389953 | |||||||
| chr7:44389972 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975+2325T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389972 | |||||||
| chr7:44390378 | A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+1919T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390378 | |||||||
| chr7:44390445 | T | C | 1 | a0001c0001t0014g0012 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.975+1852A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390445 | |||||||
| chr7:44390519 | ACCTTAGT others(1): Show |
A | 8 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(5): Show |
8 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+1770_975+1777d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390519 | |||||||
| chr7:44390586 | T | C | 1 | a0004c0004t0003g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.975+1711A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390586 | |||||||
| chr7:44390591 | T | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.975+1706A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390591 | |||||||
| chr7:44390592 | T | C | 36 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.975+1705A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390592 | |||||||
| chr7:44390652 | G | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0061 others(33): Show |
37 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.975+1645C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390652 | |||||||
| chr7:44390864 | A | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0124 others(1): Show |
4 | HG00544.hp2 HG02155.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1433T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390864 | |||||||
| chr7:44391060 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.975+1237A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391060 | |||||||
| chr7:44391150 | A | G | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+1147T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391150 | |||||||
| chr7:44391179 | A | C | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.975+1118T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391179 | |||||||
| chr7:44391230 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.975+1067C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391230 | |||||||
| chr7:44391330 | G | A | 1 | a0004c0004t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.975+967C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391330 | |||||||
| chr7:44391360 | C | T | 17 | a0001c0001t0002g0059 a0003c0003t0005g0218 a0003c0003t0005g0219 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+937G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391360 | |||||||
| chr7:44391365 | G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.975+932C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391365 | |||||||
| chr7:44391464 | G | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.975+833C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391464 | |||||||
| chr7:44391691 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.975+606G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391691 | |||||||
| chr7:44391728 | A | C | 1 | a0001c0001t0001g0045 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.975+569T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391728 | |||||||
| chr7:44391801 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.975+496T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391801 | |||||||
| chr7:44391959 | A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+338T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391959 | |||||||
| chr7:44392004 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+293C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392004 | |||||||
| chr7:44392032 | G | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.975+265C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392032 | |||||||
| chr7:44392153 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0187 |
2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.975+144A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392153 | |||||||
| chr7:44392236 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.975+61G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392236 | |||||||
| chr7:44392493 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.787-8G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44392493 | |||||||
| chr7:44392826 | A | G | 1 | a0001c0001t0035g0026 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.787-341T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44392826 | |||||||
| chr7:44393147 | C | T | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.787-662G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393147 | |||||||
| chr7:44393214 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.787-729C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393214 | |||||||
| chr7:44393247 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-762C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393247 | |||||||
| chr7:44393274 | C | T | 1 | a0001c0001t0032g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.787-789G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393274 | |||||||
| chr7:44393654 | T | C | 2 | a0001c0001t0002g0059 a0001c0001t0024g0120 |
2 | HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.787-1169A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393654 | |||||||
| chr7:44393697 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA19060.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.787-1212A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393697 | |||||||
| chr7:44393865 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0167 |
2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.787-1380G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393865 | |||||||
| chr7:44393950 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-1465G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393950 | |||||||
| chr7:44394059 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.787-1574C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394059 | |||||||
| chr7:44394179 | C | T | 2 | a0003c0003t0005g0224 a0003c0003t0005g0233 |
2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.787-1694G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394179 | |||||||
| chr7:44394345 | C | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.787-1860G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394345 | |||||||
| chr7:44394373 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.787-1888C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394373 | |||||||
| chr7:44394417 | C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.787-1932G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394417 | |||||||
| chr7:44394580 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.787-2095C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394580 | |||||||
| chr7:44394632 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.787-2147G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394632 | |||||||
| chr7:44394692 | A | C | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2207T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394692 | |||||||
| chr7:44394757 | C | T | 2 | a0003c0003t0005g0224 a0003c0003t0005g0233 |
2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.787-2272G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394757 | |||||||
| chr7:44394811 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.787-2326C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394811 | |||||||
| chr7:44394866 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.787-2381G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394866 | |||||||
| chr7:44394885 | C | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-2400G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394885 | |||||||
| chr7:44395071 | C | G | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.787-2586G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395071 | |||||||
| chr7:44395121 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-2636A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395121 | |||||||
| chr7:44395129 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.787-2644A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395129 | |||||||
| chr7:44395358 | A | C | 2 | a0001c0001t0001g0097 a0001c0001t0028g0111 |
2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.787-2873T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395358 | |||||||
| chr7:44395376 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.787-2891A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395376 | |||||||
| chr7:44395476 | A | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.787-2991T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395476 | |||||||
| chr7:44395667 | TAC | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-3184_787-3183d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395667 | |||||||
| chr7:44395670 | A | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.787-3185T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395670 | |||||||
| chr7:44396051 | T | C | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.787-3566A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396051 | |||||||
| chr7:44396087 | T | TTG | 14 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0095 others(11): Show |
14 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.787-3604_787-3603d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | T | TTGTG | 18 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(15): Show |
18 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.787-3606_787-3603d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | T | TTGTGTG | 9 | a0001c0001t0001g0034 a0002c0002t0004g0207 a0002c0002t0004g0208 others(6): Show |
9 | HG02683.hp2 HG03654.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-3608_787-3603d others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | T | TTGTGTGT others(1): Show |
2 | a0001c0001t0001g0035 a0002c0002t0023g0209 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.787-3610_787-3603d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | T | TTGTGTGT others(3): Show |
2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.787-3612_787-3603d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | T | TTGTGTGT others(7): Show |
3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.787-3616_787-3603d others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | TTG | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.787-3604_787-3603d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | TTGTG | T | 3 | a0001c0001t0002g0059 a0003c0003t0005g0218 a0003c0003t0005g0219 |
3 | HG03491.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.787-3606_787-3603d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | TTGTGTG | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0002c0002t0007g0196 others(1): Show |
4 | HG02145.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-3608_787-3603d others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | TTGTGTGT others(5): Show |
T | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-3614_787-3603d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396087 | TTGTGTGT others(7): Show |
T | 3 | a0001c0001t0002g0060 a0001c0001t0002g0077 a0001c0001t0002g0122 |
3 | HG00544.hp1 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.787-3616_787-3603d others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | |||||||
| chr7:44396113 | G | GTGTC | 3 | a0001c0001t0002g0184 a0004c0004t0003g0024 a0004c0004t0003g0025 |
3 | HG00639.hp1 HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.787-3629_787-3628i others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396113 | |||||||
| chr7:44396117 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.787-3642_787-3633d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396117 | |||||||
| chr7:44396123 | GTGT | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0114 |
2 | NA18965.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.787-3641_787-3639d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396123 | |||||||
| chr7:44396123 | GTGTT | G | 7 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(4): Show |
7 | HG02155.hp1 NA18955.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-3642_787-3639d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396123 | |||||||
| chr7:44396125 | GT | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0001g0116 others(1): Show |
4 | HG03927.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-3641delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396125 | |||||||
| chr7:44396126 | T | TG | 3 | a0001c0001t0001g0022 a0001c0001t0001g0110 a0001c0001t0001g0153 |
3 | NA18941.hp2 NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.787-3642_787-3641i others(3): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396126 | |||||||
| chr7:44396127 | T | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0126 a0001c0001t0001g0137 others(2): Show |
5 | HG00741.hp2 HG01169.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-3642A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396127 | |||||||
| chr7:44396191 | C | T | 2 | a0002c0002t0004g0214 a0002c0002t0022g0215 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.787-3706G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396191 | |||||||
| chr7:44396484 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.787-3999C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396484 | |||||||
| chr7:44396737 | C | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-4252G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396737 | |||||||
| chr7:44396786 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.787-4301G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396786 | |||||||
| chr7:44396803 | T | C | 2 | a0002c0002t0004g0213 a0002c0002t0004g0216 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.787-4318A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396803 | |||||||
| chr7:44396815 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-4330T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396815 | |||||||
| chr7:44396878 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-4393T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396878 | |||||||
| chr7:44396898 | C | T | 4 | a0001c0001t0002g0064 a0001c0001t0002g0075 a0001c0001t0002g0090 others(1): Show |
4 | HG01109.hp1 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-4413G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396898 | |||||||
| chr7:44396908 | A | G | 2 | a0003c0003t0005g0218 a0003c0003t0005g0219 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.787-4423T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396908 | |||||||
| chr7:44396948 | T | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.787-4463A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396948 | |||||||
| chr7:44396951 | TTG | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.787-4468_787-4467d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396951 | |||||||
| chr7:44397060 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.787-4575T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44397060 | |||||||
| chr7:44398086 | T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-5601A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398086 | |||||||
| chr7:44398321 | G | A | 2 | a0001c0001t0013g0071 a0001c0001t0013g0123 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.787-5836C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398321 | |||||||
| chr7:44398827 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+5613C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398827 | |||||||
| chr7:44398991 | T | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.786+5449A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398991 | |||||||
| chr7:44399024 | T | C | 3 | a0002c0002t0023g0209 a0002c0005t0012g0235 a0002c0005t0012g0236 |
3 | HG02922.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.786+5416A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399024 | |||||||
| chr7:44399103 | C | T | 1 | a0001c0001t0003g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.786+5337G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399103 | |||||||
| chr7:44399160 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0140 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.786+5280C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399160 | |||||||
| chr7:44399279 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+5161A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399279 | |||||||
| chr7:44399498 | G | A | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4942C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399498 | |||||||
| chr7:44399621 | A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+4819T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399621 | |||||||
| chr7:44399633 | T | C | 42 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.786+4807A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399633 | |||||||
| chr7:44399689 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.786+4751C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399689 | |||||||
| chr7:44399914 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.786+4526T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399914 | |||||||
| chr7:44399988 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0031g0103 |
3 | HG01070.hp1 HG01081.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.786+4452A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399988 | |||||||
| chr7:44399996 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+4444G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399996 | |||||||
| chr7:44400417 | A | G | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4023T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400417 | |||||||
| chr7:44400758 | C | T | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3682G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400758 | |||||||
| chr7:44400899 | T | C | 1 | a0001c0001t0003g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.786+3541A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400899 | |||||||
| chr7:44400952 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+3488G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400952 | |||||||
| chr7:44400953 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.786+3487G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400953 | |||||||
| chr7:44401100 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786+3340C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401100 | |||||||
| chr7:44401185 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+3255G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401185 | |||||||
| chr7:44401186 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+3254G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401186 | |||||||
| chr7:44401199 | C | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.786+3241G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401199 | |||||||
| chr7:44401206 | C | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.786+3234G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401206 | |||||||
| chr7:44401416 | T | C | 1 | a0002c0002t0004g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.786+3024A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401416 | |||||||
| chr7:44401429 | C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+3011G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401429 | |||||||
| chr7:44401572 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.786+2868G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401572 | |||||||
| chr7:44402056 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.786+2384A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402056 | |||||||
| chr7:44402067 | G | T | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.786+2373C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402067 | |||||||
| chr7:44402410 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.786+2030G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402410 | |||||||
| chr7:44402675 | G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786+1765C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402675 | |||||||
| chr7:44402697 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.786+1743T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402697 | |||||||
| chr7:44403000 | T | C | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.786+1440A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403000 | |||||||
| chr7:44403068 | G | A | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.786+1372C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403068 | |||||||
| chr7:44403081 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.786+1359C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403081 | |||||||
| chr7:44403135 | C | T | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.786+1305G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403135 | |||||||
| chr7:44403231 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+1209A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403231 | |||||||
| chr7:44403304 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+1136A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403304 | |||||||
| chr7:44403514 | C | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786+926G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403514 | |||||||
| chr7:44403544 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+896G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403544 | |||||||
| chr7:44403546 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.786+894A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403546 | |||||||
| chr7:44403559 | G | A | 5 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 others(2): Show |
5 | HG02257.hp1 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+881C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403559 | |||||||
| chr7:44403572 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.786+868C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403572 | |||||||
| chr7:44403777 | T | A | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.786+663A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403777 | |||||||
| chr7:44403831 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+609C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403831 | |||||||
| chr7:44403856 | A | G | 8 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(5): Show |
8 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+584T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403856 | |||||||
| chr7:44404138 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.786+302G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44404138 | |||||||
| chr7:44404171 | G | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.786+269C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44404171 | |||||||
| chr7:44404712 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.643-129G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44404712 | |||||||
| chr7:44404969 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.643-386T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44404969 | |||||||
| chr7:44405103 | T | C | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.643-520A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405103 | |||||||
| chr7:44405250 | C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-667G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405250 | |||||||
| chr7:44405305 | C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-722G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405305 | |||||||
| chr7:44405343 | G | A | 2 | a0001c0001t0003g0175 a0001c0001t0003g0176 |
2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.643-760C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405343 | |||||||
| chr7:44405487 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-904A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405487 | |||||||
| chr7:44405885 | C | T | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-1302G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405885 | |||||||
| chr7:44406124 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.643-1541A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406124 | |||||||
| chr7:44406185 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.643-1602C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406185 | |||||||
| chr7:44406248 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.643-1665A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406248 | |||||||
| chr7:44406252 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-1669G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406252 | |||||||
| chr7:44406481 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0037g0080 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.643-1898T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406481 | |||||||
| chr7:44406536 | C | A | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.643-1953G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406536 | |||||||
| chr7:44406782 | G | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-2199C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406782 | |||||||
| chr7:44406786 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.643-2203T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406786 | |||||||
| chr7:44406805 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.643-2222C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406805 | |||||||
| chr7:44406883 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.643-2300T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406883 | |||||||
| chr7:44406976 | C | T | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2393G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406976 | |||||||
| chr7:44407028 | A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-2445T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407028 | |||||||
| chr7:44407052 | G | A | 2 | a0002c0002t0004g0214 a0002c0002t0022g0215 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.643-2469C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407052 | |||||||
| chr7:44407185 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2602C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407185 | |||||||
| chr7:44407202 | C | T | 8 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.643-2619G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407202 | |||||||
| chr7:44407269 | T | TA | 44 | a0001c0001t0001g0034 a0002c0002t0004g0207 a0002c0002t0004g0208 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.643-2687dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407269 | |||||||
| chr7:44407431 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-2848C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407431 | |||||||
| chr7:44407459 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2876C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407459 | |||||||
| chr7:44407466 | G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.643-2883C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407466 | |||||||
| chr7:44407566 | C | CA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0053 others(9): Show |
12 | HG01358.hp1 HG01496.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.643-2984dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407566 | |||||||
| chr7:44407578 | A | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.643-2995T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407578 | |||||||
| chr7:44407688 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.643-3105A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407688 | |||||||
| chr7:44407957 | A | C | 2 | a0001c0001t0017g0067 a0001c0001t0017g0068 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.643-3374T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407957 | |||||||
| chr7:44408182 | A | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-3599T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408182 | |||||||
| chr7:44408335 | C | T | 1 | a0002c0002t0008g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.643-3752G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408335 | |||||||
| chr7:44408625 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-4042T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408625 | |||||||
| chr7:44409036 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.643-4453C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409036 | |||||||
| chr7:44409044 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0030g0180 |
2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.643-4461T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409044 | |||||||
| chr7:44409067 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.643-4484C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409067 | |||||||
| chr7:44409328 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.643-4745A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409328 | |||||||
| chr7:44409565 | C | CA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0045 others(14): Show |
17 | HG00741.hp2 HG01496.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-4983dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409565 | |||||||
| chr7:44409863 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5280T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409863 | |||||||
| chr7:44409902 | C | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.643-5319G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409902 | |||||||
| chr7:44409994 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0089 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.643-5411C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409994 | |||||||
| chr7:44410052 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5469G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410052 | |||||||
| chr7:44410329 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5746A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410329 | |||||||
| chr7:44410695 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-6112T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410695 | |||||||
| chr7:44410770 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0171 a0001c0001t0001g0182 others(1): Show |
4 | NA18965.hp1 NA18989.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-6187A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410770 | |||||||
| chr7:44410785 | G | T | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.643-6202C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410785 | |||||||
| chr7:44410923 | G | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
10 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-6340C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410923 | |||||||
| chr7:44411063 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.643-6480T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411063 | |||||||
| chr7:44411230 | C | T | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.643-6647G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411230 | |||||||
| chr7:44411307 | T | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0046 |
2 | HG01981.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.643-6724A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411307 | |||||||
| chr7:44411704 | T | C | 2 | a0003c0003t0005g0222 a0003c0003t0005g0223 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.643-7121A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411704 | |||||||
| chr7:44411731 | G | C | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.643-7148C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411731 | |||||||
| chr7:44411822 | T | G | 1 | a0001c0001t0024g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.643-7239A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411822 | |||||||
| chr7:44412092 | G | T | 1 | a0001c0001t0001g0011 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.643-7509C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412092 | |||||||
| chr7:44412095 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.643-7512G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412095 | |||||||
| chr7:44412513 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-7930C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412513 | |||||||
| chr7:44412694 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.643-8111C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412694 | |||||||
| chr7:44412716 | AG | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-8134delC | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412716 | |||||||
| chr7:44412782 | T | C | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.643-8199A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412782 | |||||||
| chr7:44412926 | C | CAA | 10 | a0001c0001t0001g0174 a0002c0002t0004g0207 a0002c0002t0004g0208 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-8345_643-8344d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412926 | C | CAAA | 5 | a0002c0002t0004g0210 a0002c0002t0004g0212 a0002c0002t0007g0196 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-8346_643-8344d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412926 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0010g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.643-8353_643-8344d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412926 | C | CAAAAAAA others(4): Show |
1 | a0002c0002t0010g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.643-8354_643-8344d others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412926 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0168 |
2 | HG01516.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.643-8355_643-8344d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412926 | CAAAAAAA others(10): Show |
C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.643-8360_643-8344d others(19): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | |||||||
| chr7:44412932 | AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-8360_643-8350d others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412932 | |||||||
| chr7:44412943 | G | A | 34 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.643-8360C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412943 | |||||||
| chr7:44412951 | A | AAG | 11 | a0002c0002t0011g0194 a0002c0002t0011g0195 a0003c0003t0005g0218 others(8): Show |
11 | HG00280.hp1 HG00280.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-8369_643-8368i others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412951 | |||||||
| chr7:44412951 | A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-8368T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412951 | |||||||
| chr7:44413039 | G | C | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.643-8456C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413039 | |||||||
| chr7:44413297 | A | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0033 others(4): Show |
7 | HG01993.hp2 HG02293.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-8714T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413297 | |||||||
| chr7:44413407 | A | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-8824T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413407 | |||||||
| chr7:44413558 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.643-8975G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413558 | |||||||
| chr7:44413702 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0028g0111 |
2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.643-9119A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413702 | |||||||
| chr7:44413737 | T | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-9154A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413737 | |||||||
| chr7:44413774 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.643-9191G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413774 | |||||||
| chr7:44413775 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.643-9192C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413775 | |||||||
| chr7:44413928 | G | A | 31 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0048 others(28): Show |
31 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.643-9345C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413928 | |||||||
| chr7:44413955 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.643-9372A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413955 | |||||||
| chr7:44414089 | G | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.643-9506C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414089 | |||||||
| chr7:44414381 | G | T | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-9798C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414381 | |||||||
| chr7:44414462 | C | T | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-9879G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414462 | |||||||
| chr7:44414508 | T | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.643-9925A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414508 | |||||||
| chr7:44414626 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-10043G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414626 | |||||||
| chr7:44414776 | T | C | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.643-10193A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414776 | |||||||
| chr7:44414892 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.643-10309A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414892 | |||||||
| chr7:44414903 | C | T | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-10320G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414903 | |||||||
| chr7:44415238 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-10655A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415238 | |||||||
| chr7:44415333 | A | AAG | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-10752_643-1075 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415333 | |||||||
| chr7:44415357 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-10774A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415357 | |||||||
| chr7:44415428 | T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-10845A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415428 | |||||||
| chr7:44415487 | T | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.643-10904A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415487 | |||||||
| chr7:44416043 | A | G | 6 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(3): Show |
6 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-11460T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416043 | |||||||
| chr7:44416222 | T | C | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+11349A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416222 | |||||||
| chr7:44416234 | C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+11337G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416234 | |||||||
| chr7:44416263 | C | T | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.642+11308G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416263 | |||||||
| chr7:44416327 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+11244T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416327 | |||||||
| chr7:44416470 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.642+11101A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416470 | |||||||
| chr7:44416930 | C | CT | 2 | a0004c0004t0003g0024 a0004c0004t0003g0025 |
2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.642+10640dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416930 | |||||||
| chr7:44417172 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0062 |
2 | HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.642+10399C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417172 | |||||||
| chr7:44417291 | C | T | 44 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.642+10280G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417291 | |||||||
| chr7:44417700 | C | A | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+9871G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417700 | |||||||
| chr7:44417800 | C | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0178 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.642+9771G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417800 | |||||||
| chr7:44417914 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+9657A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417914 | |||||||
| chr7:44418065 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.642+9506A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418065 | |||||||
| chr7:44418273 | C | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(37): Show |
40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.642+9298G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418273 | |||||||
| chr7:44418485 | A | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+9086T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418485 | |||||||
| chr7:44418518 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0178 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.642+9053A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418518 | |||||||
| chr7:44418796 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.642+8775G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418796 | |||||||
| chr7:44418875 | A | G | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.642+8696T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418875 | |||||||
| chr7:44419014 | A | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+8557T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419014 | |||||||
| chr7:44419224 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.642+8347C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419224 | |||||||
| chr7:44419497 | GCTAAGGG others(9): Show |
G | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+8058_642+8073d others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419497 | |||||||
| chr7:44420152 | C | G | 8 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+7419G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420152 | |||||||
| chr7:44420216 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+7355G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420216 | |||||||
| chr7:44420491 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.642+7080A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420491 | |||||||
| chr7:44420546 | C | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+7025G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420546 | |||||||
| chr7:44420627 | G | A | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.642+6944C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420627 | |||||||
| chr7:44420782 | T | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+6789A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420782 | |||||||
| chr7:44420874 | G | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.642+6697C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420874 | |||||||
| chr7:44420888 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.642+6683G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420888 | |||||||
| chr7:44420900 | A | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.642+6671T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420900 | |||||||
| chr7:44421073 | C | T | 8 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+6498G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421073 | |||||||
| chr7:44421088 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0050 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+6483G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421088 | |||||||
| chr7:44421115 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.642+6456G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421115 | |||||||
| chr7:44421266 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+6305T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421266 | |||||||
| chr7:44421331 | T | TA | 166 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
167 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.642+6239dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | |||||||
| chr7:44421331 | T | TAA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0093 a0001c0001t0001g0108 others(10): Show |
13 | HG00438.hp2 HG01106.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+6238_642+6239d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | |||||||
| chr7:44421331 | TA | T | 17 | a0002c0002t0021g0217 a0002c0002t0023g0209 a0002c0002t0040g0237 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+6239delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | |||||||
| chr7:44421487 | C | CA | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
158 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.642+6083dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421487 | |||||||
| chr7:44421487 | CA | C | 19 | a0001c0001t0002g0189 a0002c0002t0021g0217 a0002c0005t0012g0235 others(16): Show |
19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+6083delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421487 | |||||||
| chr7:44421655 | C | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+5916G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421655 | |||||||
| chr7:44421675 | T | C | 1 | a0002c0002t0018g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.642+5896A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421675 | |||||||
| chr7:44421759 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.642+5812C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421759 | |||||||
| chr7:44421919 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.642+5652C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421919 | |||||||
| chr7:44422278 | T | C | 1 | a0005c0007t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.642+5293A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422278 | |||||||
| chr7:44422350 | G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+5221C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422350 | |||||||
| chr7:44422679 | G | A | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+4892C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422679 | |||||||
| chr7:44422714 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+4857C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422714 | |||||||
| chr7:44422944 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.642+4627G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422944 | |||||||
| chr7:44423011 | C | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+4560G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423011 | |||||||
| chr7:44423257 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+4314G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423257 | |||||||
| chr7:44423326 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.642+4245G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423326 | |||||||
| chr7:44423336 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+4235C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423336 | |||||||
| chr7:44423377 | G | T | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.642+4194C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423377 | |||||||
| chr7:44423532 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.642+4039G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423532 | |||||||
| chr7:44423696 | T | G | 1 | a0001c0001t0001g0011 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.642+3875A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423696 | |||||||
| chr7:44423734 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+3837G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423734 | |||||||
| chr7:44424054 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+3517G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424054 | |||||||
| chr7:44424224 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.642+3347G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424224 | |||||||
| chr7:44424492 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.642+3079G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424492 | |||||||
| chr7:44424532 | G | A | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.642+3039C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424532 | |||||||
| chr7:44424549 | T | A | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.642+3022A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424549 | |||||||
| chr7:44424553 | T | G | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.642+3018A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424553 | |||||||
| chr7:44424620 | T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+2951A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424620 | |||||||
| chr7:44424684 | T | C | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.642+2887A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424684 | |||||||
| chr7:44424963 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.642+2608A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424963 | |||||||
| chr7:44425216 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.642+2355C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425216 | |||||||
| chr7:44425395 | G | A | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+2176C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425395 | |||||||
| chr7:44425523 | G | T | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.642+2048C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425523 | |||||||
| chr7:44425525 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+2046A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425525 | |||||||
| chr7:44425666 | C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1905G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425666 | |||||||
| chr7:44425669 | G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1902C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425669 | |||||||
| chr7:44425779 | T | C | 2 | a0003c0003t0005g0224 a0003c0003t0005g0233 |
2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.642+1792A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425779 | |||||||
| chr7:44425817 | G | A | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+1754C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425817 | |||||||
| chr7:44425849 | G | A | 1 | a0003c0003t0009g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.642+1722C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425849 | |||||||
| chr7:44426507 | G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1064C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426507 | |||||||
| chr7:44426518 | C | T | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+1053G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426518 | |||||||
| chr7:44426522 | C | T | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.642+1049G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426522 | |||||||
| chr7:44426553 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1018A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426553 | |||||||
| chr7:44426572 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+999C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426572 | |||||||
| chr7:44426613 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+958T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426613 | |||||||
| chr7:44426772 | G | C | 1 | a0001c0001t0037g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.642+799C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426772 | |||||||
| chr7:44426779 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+792C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426779 | |||||||
| chr7:44426795 | C | CA | 6 | a0001c0001t0001g0045 a0001c0001t0001g0136 a0001c0001t0001g0140 others(3): Show |
6 | HG01981.hp1 HG02572.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+775dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426795 | |||||||
| chr7:44426868 | T | A | 6 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(3): Show |
6 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+703A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426868 | |||||||
| chr7:44427130 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.642+441A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427130 | |||||||
| chr7:44427161 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.642+410G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427161 | |||||||
| chr7:44427277 | A | G | 42 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.642+294T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427277 | |||||||
| chr7:44427534 | G | A | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.642+37C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427534 | |||||||
| chr7:44427798 | C | A | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510-95G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44427798 | |||||||
| chr7:44427833 | C | T | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-130G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44427833 | |||||||
| chr7:44428116 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-413G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428116 | |||||||
| chr7:44428123 | T | TA | 20 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0001c0001t0002g0010 others(17): Show |
20 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.510-421dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428123 | |||||||
| chr7:44428123 | TA | T | 34 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.510-421delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428123 | |||||||
| chr7:44428334 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-631C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428334 | |||||||
| chr7:44428363 | G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.510-660C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428363 | |||||||
| chr7:44428456 | G | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-753C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428456 | |||||||
| chr7:44428593 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-890A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428593 | |||||||
| chr7:44428722 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1019G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428722 | |||||||
| chr7:44428723 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1020G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428723 | |||||||
| chr7:44428724 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1021T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428724 | |||||||
| chr7:44428726 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1023T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428726 | |||||||
| chr7:44428727 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1024T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428727 | |||||||
| chr7:44428729 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1026T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428729 | |||||||
| chr7:44428731 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1028C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428731 | |||||||
| chr7:44428732 | TAACAATG others(36): Show |
T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1072_510-1030d others(45): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428732 | |||||||
| chr7:44428777 | G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1074C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428777 | |||||||
| chr7:44428779 | C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1076G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428779 | |||||||
| chr7:44428780 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1077G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428780 | |||||||
| chr7:44428787 | G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1084C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428787 | |||||||
| chr7:44428789 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1086C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428789 | |||||||
| chr7:44428792 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1089G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428792 | |||||||
| chr7:44428797 | G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1094C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428797 | |||||||
| chr7:44428963 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-1260T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428963 | |||||||
| chr7:44429413 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510-1710A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429413 | |||||||
| chr7:44429426 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0115 |
2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.510-1723C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429426 | |||||||
| chr7:44429534 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.510-1831G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429534 | |||||||
| chr7:44429689 | A | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-1986T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429689 | |||||||
| chr7:44429700 | G | A | 1 | a0001c0001t0017g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.510-1997C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429700 | |||||||
| chr7:44430062 | C | T | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-2359G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430062 | |||||||
| chr7:44430131 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-2428A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430131 | |||||||
| chr7:44430151 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0182 a0001c0006t0001g0149 |
3 | NA18965.hp1 NA18989.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.510-2448A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430151 | |||||||
| chr7:44430394 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2691A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430394 | |||||||
| chr7:44430481 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-2778G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430481 | |||||||
| chr7:44430551 | T | TAC | 2 | a0002c0002t0004g0212 a0003c0003t0019g0230 |
2 | HG00280.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.510-2850_510-2849d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | |||||||
| chr7:44430551 | TACCCACA others(5): Show |
T | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.510-2860_510-2849d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | |||||||
| chr7:44430551 | TACCCACA others(9): Show |
T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-2864_510-2849d others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | |||||||
| chr7:44430552 | ACC | A | 5 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0211 others(2): Show |
5 | HG02683.hp2 HG02922.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-2851_510-2850d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430552 | |||||||
| chr7:44430554 | C | A | 6 | a0002c0002t0004g0212 a0002c0002t0007g0198 a0002c0002t0010g0193 others(3): Show |
6 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-2851G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | |||||||
| chr7:44430554 | C | CCA | 7 | a0001c0001t0030g0180 a0002c0002t0008g0205 a0003c0003t0006g0227 others(4): Show |
7 | HG00438.hp1 HG01358.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2853_510-2852d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | |||||||
| chr7:44430554 | C | CCACA | 6 | a0002c0002t0004g0210 a0002c0002t0008g0204 a0002c0002t0008g0206 others(3): Show |
6 | HG01106.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-2855_510-2852d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | |||||||
| chr7:44430558 | ACACACAC others(5): Show |
A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2867_510-2856d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430558 | |||||||
| chr7:44430560 | ACACACAC others(3): Show |
A | 3 | a0002c0002t0011g0194 a0002c0002t0011g0195 a0002c0002t0040g0237 |
3 | HG02486.hp2 HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-2867_510-2858d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430560 | |||||||
| chr7:44430562 | ACACACAC others(1): Show |
A | 2 | a0003c0003t0005g0218 a0003c0003t0005g0219 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-2867_510-2860d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430562 | |||||||
| chr7:44430566 | ACACT | A | 2 | a0003c0003t0005g0221 a0003c0003t0005g0225 |
2 | HG00099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.510-2867_510-2864d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430566 | |||||||
| chr7:44430568 | ACT | A | 4 | a0002c0002t0004g0213 a0002c0002t0004g0214 a0002c0002t0004g0216 others(1): Show |
4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-2867_510-2866d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430568 | |||||||
| chr7:44430570 | T | A | 31 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(28): Show |
31 | HG00280.hp2 HG00438.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.510-2867A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430570 | T | TCA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG01109.hp1 HG01257.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.510-2869_510-2868d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430570 | T | TCACA | 3 | a0001c0001t0001g0118 a0001c0001t0001g0179 a0001c0001t0002g0075 |
3 | HG01358.hp1 HG02738.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.510-2871_510-2868d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430570 | TCA | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0101 others(5): Show |
8 | HG01943.hp1 HG03209.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-2869_510-2868d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430570 | TCACA | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0117 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-2871_510-2868d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430570 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0100 |
3 | HG03130.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.510-2875_510-2868d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | |||||||
| chr7:44430604 | A | AC | 2 | a0001c0001t0001g0095 a0001c0001t0001g0148 |
2 | NA18955.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.510-2902_510-2901i others(3): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430604 | |||||||
| chr7:44430605 | A | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-2902T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430605 | |||||||
| chr7:44430717 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0014g0012 |
2 | HG00673.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.510-3014G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430717 | |||||||
| chr7:44430742 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510-3039G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430742 | |||||||
| chr7:44430764 | T | C | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-3061A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430764 | |||||||
| chr7:44430938 | C | T | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510-3235G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430938 | |||||||
| chr7:44430980 | A | G | 3 | a0002c0002t0021g0217 a0002c0002t0023g0209 a0002c0002t0040g0237 |
3 | HG03130.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-3277T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430980 | |||||||
| chr7:44431020 | A | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-3317T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431020 | |||||||
| chr7:44431181 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG01168.hp1 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.510-3478G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431181 | |||||||
| chr7:44431215 | G | A | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.510-3512C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431215 | |||||||
| chr7:44431249 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-3546C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431249 | |||||||
| chr7:44431458 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-3755G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431458 | |||||||
| chr7:44431545 | C | G | 11 | a0001c0001t0001g0048 a0001c0001t0001g0092 a0001c0001t0001g0098 others(8): Show |
11 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-3842G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431545 | |||||||
| chr7:44431653 | G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-3950C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431653 | |||||||
| chr7:44431668 | C | CT | 12 | a0001c0001t0001g0112 a0001c0001t0001g0119 a0001c0001t0001g0157 others(9): Show |
12 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-3966dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | |||||||
| chr7:44431668 | C | CTT | 16 | a0002c0002t0004g0210 a0003c0003t0005g0218 a0003c0003t0005g0219 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-3967_510-3966d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | |||||||
| chr7:44431668 | CT | C | 15 | a0001c0001t0001g0101 a0001c0001t0001g0154 a0001c0001t0002g0060 others(12): Show |
15 | HG00741.hp2 HG01943.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.510-3966delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | |||||||
| chr7:44431759 | A | G | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-4056T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431759 | |||||||
| chr7:44431842 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(30): Show |
33 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.510-4139A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431842 | |||||||
| chr7:44431962 | G | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0098 a0001c0001t0001g0108 |
3 | NA18960.hp1 NA18965.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.510-4259C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431962 | |||||||
| chr7:44432098 | C | T | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-4395G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432098 | |||||||
| chr7:44432214 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-4511A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432214 | |||||||
| chr7:44432215 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.510-4512T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432215 | |||||||
| chr7:44432354 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-4651C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432354 | |||||||
| chr7:44432505 | C | T | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-4802G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432505 | |||||||
| chr7:44432533 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-4830C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432533 | |||||||
| chr7:44432592 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-4889C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432592 | |||||||
| chr7:44432619 | C | T | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.510-4916G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432619 | |||||||
| chr7:44432802 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0157 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.510-5099A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432802 | |||||||
| chr7:44433262 | A | ATG | 14 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0044 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-5561_510-5560d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433262 | |||||||
| chr7:44433354 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.510-5651G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433354 | |||||||
| chr7:44433398 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.510-5695C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433398 | |||||||
| chr7:44433453 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA18941.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.510-5750A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433453 | |||||||
| chr7:44433514 | A | AGT | 3 | a0001c0001t0001g0095 a0002c0002t0010g0193 a0002c0002t0010g0201 |
3 | HG00741.hp2 HG03139.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.510-5813_510-5812d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433514 | |||||||
| chr7:44433598 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510-5895C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433598 | |||||||
| chr7:44433600 | A | G | 26 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.510-5897T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433600 | |||||||
| chr7:44433608 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-5905A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433608 | |||||||
| chr7:44433850 | C | A | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-6147G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433850 | |||||||
| chr7:44434020 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-6317C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434020 | |||||||
| chr7:44434220 | TGCCTGGA others(57): Show |
T | 1 | a0005c0007t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.510-6581_510-6518d others(66): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434220 | |||||||
| chr7:44434265 | A | G | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-6562T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434265 | |||||||
| chr7:44434421 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-6718C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434421 | |||||||
| chr7:44434517 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0003g0031 |
2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.510-6814A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434517 | |||||||
| chr7:44434700 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.510-6997T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434700 | |||||||
| chr7:44435021 | G | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-7318C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435021 | |||||||
| chr7:44435023 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-7320C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435023 | |||||||
| chr7:44435049 | T | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-7346A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435049 | |||||||
| chr7:44435072 | T | G | 1 | a0002c0002t0004g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.510-7369A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435072 | |||||||
| chr7:44435092 | CTTT | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-7392_510-7390d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435092 | |||||||
| chr7:44435278 | A | G | 2 | a0002c0002t0004g0213 a0002c0002t0004g0216 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.510-7575T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435278 | |||||||
| chr7:44435310 | C | T | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-7607G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435310 | |||||||
| chr7:44435324 | G | A | 3 | a0001c0001t0001g0034 a0002c0005t0012g0235 a0002c0005t0012g0236 |
3 | HG02922.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.510-7621C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435324 | |||||||
| chr7:44435363 | G | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510-7660C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435363 | |||||||
| chr7:44435668 | C | G | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-7965G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435668 | |||||||
| chr7:44435909 | G | C | 2 | a0001c0001t0001g0179 a0001c0001t0037g0080 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.510-8206C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435909 | |||||||
| chr7:44436151 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-8448G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436151 | |||||||
| chr7:44436332 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-8629G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436332 | |||||||
| chr7:44436347 | T | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-8644A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436347 | |||||||
| chr7:44436367 | G | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-8664C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436367 | |||||||
| chr7:44436445 | G | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-8742C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436445 | |||||||
| chr7:44436506 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-8803C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436506 | |||||||
| chr7:44436701 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.510-8998A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436701 | |||||||
| chr7:44436785 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0178 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.510-9082A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436785 | |||||||
| chr7:44436810 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.510-9107T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436810 | |||||||
| chr7:44436815 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-9112A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436815 | |||||||
| chr7:44436854 | T | C | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-9151A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436854 | |||||||
| chr7:44436891 | A | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-9188T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436891 | |||||||
| chr7:44437054 | TTTTTC | T | 3 | a0002c0002t0008g0206 a0002c0002t0011g0194 a0002c0002t0011g0195 |
3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.510-9356_510-9352d others(7): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437054 | |||||||
| chr7:44437069 | C | CT | 22 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0001c0001t0001g0130 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.510-9367dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437069 | |||||||
| chr7:44437171 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-9468C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437171 | |||||||
| chr7:44437201 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.510-9498G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437201 | |||||||
| chr7:44437218 | T | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-9515A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437218 | |||||||
| chr7:44437255 | A | G | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-9552T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437255 | |||||||
| chr7:44437270 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0109 |
2 | HG02145.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.510-9567T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437270 | |||||||
| chr7:44437386 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-9683A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437386 | |||||||
| chr7:44437528 | AGAG | A | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-9828_510-9826d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437528 | |||||||
| chr7:44437576 | C | T | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-9873G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437576 | |||||||
| chr7:44438093 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-10390G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438093 | |||||||
| chr7:44438348 | C | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.510-10645G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438348 | |||||||
| chr7:44438419 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-10716T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438419 | |||||||
| chr7:44438513 | G | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-10810C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438513 | |||||||
| chr7:44438689 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-10986G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438689 | |||||||
| chr7:44438842 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.510-11139C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438842 | |||||||
| chr7:44438983 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-11280G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438983 | |||||||
| chr7:44439055 | G | A | 2 | a0003c0003t0005g0218 a0003c0003t0005g0219 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-11352C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439055 | |||||||
| chr7:44439096 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-11393C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439096 | |||||||
| chr7:44439287 | G | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-11584C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439287 | |||||||
| chr7:44439328 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.510-11625T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439328 | |||||||
| chr7:44439344 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.510-11641T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439344 | |||||||
| chr7:44439578 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-11875T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439578 | |||||||
| chr7:44439843 | A | C | 1 | a0001c0001t0003g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.510-12140T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439843 | |||||||
| chr7:44439868 | T | C | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-12165A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439868 | |||||||
| chr7:44439889 | GCTAA | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-12190_510-1218 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439889 | |||||||
| chr7:44439935 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
30 | HG00544.hp2 HG00639.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.510-12232T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439935 | |||||||
| chr7:44440118 | C | T | 1 | a0004c0004t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510-12415G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440118 | |||||||
| chr7:44440496 | G | GA | 24 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0034 others(21): Show |
24 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.510-12794dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440496 | G | GAAAAAAA others(1): Show |
7 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(4): Show |
7 | HG00280.hp2 HG00438.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-12801_510-1279 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440496 | G | GAAAAAAA others(2): Show |
6 | a0003c0003t0005g0219 a0003c0003t0005g0221 a0003c0003t0005g0224 others(3): Show |
6 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-12802_510-1279 others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440496 | G | GAAAAAAA others(3): Show |
2 | a0003c0003t0005g0218 a0003c0003t0005g0222 |
2 | HG01256.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-12803_510-1279 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440496 | G | GAAAAAAA others(4): Show |
1 | a0003c0003t0005g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.510-12804_510-1279 others(15): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440496 | GA | G | 12 | a0001c0001t0001g0045 a0002c0002t0004g0207 a0002c0002t0004g0208 others(9): Show |
12 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-12794delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | |||||||
| chr7:44440549 | AT | A | 18 | a0001c0001t0026g0186 a0002c0002t0021g0217 a0002c0002t0040g0237 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-12847delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440549 | |||||||
| chr7:44440594 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.510-12891T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440594 | |||||||
| chr7:44440596 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-12893T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440596 | |||||||
| chr7:44440688 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0114 |
2 | NA18612.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.510-12985A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440688 | |||||||
| chr7:44440865 | C | T | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-13162G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440865 | |||||||
| chr7:44440888 | T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-13185A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440888 | |||||||
| chr7:44440951 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-13248T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440951 | |||||||
| chr7:44440954 | C | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-13251G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440954 | |||||||
| chr7:44441081 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-13378C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441081 | |||||||
| chr7:44441091 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-13388T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441091 | |||||||
| chr7:44441244 | A | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-13541T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441244 | |||||||
| chr7:44441545 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0003g0031 |
2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.510-13842A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441545 | |||||||
| chr7:44441554 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-13851C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441554 | |||||||
| chr7:44441673 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02698.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-13970G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441673 | |||||||
| chr7:44441674 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-13971C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441674 | |||||||
| chr7:44441768 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-14065C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441768 | |||||||
| chr7:44441907 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-14204G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441907 | |||||||
| chr7:44441937 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-14234G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441937 | |||||||
| chr7:44442025 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-14322G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442025 | |||||||
| chr7:44442038 | A | G | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.510-14335T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442038 | |||||||
| chr7:44442111 | C | T | 2 | a0003c0003t0019g0230 a0003c0003t0019g0232 |
2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.510-14408G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442111 | |||||||
| chr7:44442389 | A | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0074 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-14686T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442389 | |||||||
| chr7:44442693 | C | CT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0020 others(44): Show |
47 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-14991dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442693 | |||||||
| chr7:44442693 | CT | C | 22 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0001t0002g0010 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.510-14991delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442693 | |||||||
| chr7:44442699 | T | C | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-14996A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442699 | |||||||
| chr7:44442732 | T | G | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-15029A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442732 | |||||||
| chr7:44442734 | G | C | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-15031C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442734 | |||||||
| chr7:44442797 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0140 |
2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510-15094C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442797 | |||||||
| chr7:44443607 | C | T | 2 | a0003c0003t0019g0230 a0003c0003t0019g0232 |
2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.510-15904G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443607 | |||||||
| chr7:44443628 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-15925G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443628 | |||||||
| chr7:44443661 | G | A | 13 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(10): Show |
13 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.510-15958C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443661 | |||||||
| chr7:44443702 | A | C | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.510-15999T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443702 | |||||||
| chr7:44443974 | T | C | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-16271A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443974 | |||||||
| chr7:44444185 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-16482G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444185 | |||||||
| chr7:44444263 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-16560T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444263 | |||||||
| chr7:44444371 | G | A | 14 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0092 others(11): Show |
14 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-16668C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444371 | |||||||
| chr7:44444631 | G | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-16928C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444631 | |||||||
| chr7:44444667 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG02280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-16964A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444667 | |||||||
| chr7:44444886 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510-17183G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444886 | |||||||
| chr7:44444952 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-17249T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444952 | |||||||
| chr7:44445159 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-17456A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445159 | |||||||
| chr7:44445169 | A | G | 2 | a0002c0002t0004g0213 a0002c0002t0004g0216 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.510-17466T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445169 | |||||||
| chr7:44445255 | C | T | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510-17552G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445255 | |||||||
| chr7:44445299 | A | G | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-17596T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445299 | |||||||
| chr7:44445398 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510-17695T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445398 | |||||||
| chr7:44445426 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-17723A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445426 | |||||||
| chr7:44445436 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-17733C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445436 | |||||||
| chr7:44445481 | C | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.510-17778G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445481 | |||||||
| chr7:44445750 | G | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-18047C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445750 | |||||||
| chr7:44445992 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-18289A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445992 | |||||||
| chr7:44446106 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-18403G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446106 | |||||||
| chr7:44446692 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-18989G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446692 | |||||||
| chr7:44446955 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.510-19252A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446955 | |||||||
| chr7:44447139 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-19436T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447139 | |||||||
| chr7:44447199 | G | A | 2 | a0002c0002t0004g0210 a0002c0002t0004g0212 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.510-19496C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447199 | |||||||
| chr7:44447281 | C | T | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-19578G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447281 | |||||||
| chr7:44447322 | G | A | 2 | a0002c0002t0004g0214 a0002c0002t0022g0215 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.510-19619C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447322 | |||||||
| chr7:44447345 | C | T | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.510-19642G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447345 | |||||||
| chr7:44447414 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-19711T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447414 | |||||||
| chr7:44447490 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA18941.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.510-19787C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447490 | |||||||
| chr7:44447778 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510-20075T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447778 | |||||||
| chr7:44447931 | T | C | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-20228A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447931 | |||||||
| chr7:44448287 | T | C | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-20584A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448287 | |||||||
| chr7:44448288 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-20585C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448288 | |||||||
| chr7:44448288 | G | T | 1 | a0001c0001t0002g0059 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-20585C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448288 | |||||||
| chr7:44448502 | G | A | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510-20799C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448502 | |||||||
| chr7:44448701 | C | T | 2 | a0002c0002t0020g0203 a0002c0002t0038g0202 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.510-20998G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448701 | |||||||
| chr7:44449049 | A | G | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-21346T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449049 | |||||||
| chr7:44449088 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-21385G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449088 | |||||||
| chr7:44449240 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-21537C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449240 | |||||||
| chr7:44449578 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-21875C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449578 | |||||||
| chr7:44449852 | TA | T | 34 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.510-22150delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449852 | |||||||
| chr7:44449922 | T | C | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-22219A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449922 | |||||||
| chr7:44450061 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.510-22358G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450061 | |||||||
| chr7:44450175 | T | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG00735.hp1 HG01928.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-22472A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450175 | |||||||
| chr7:44450179 | A | AT | 11 | a0001c0001t0001g0073 a0001c0001t0001g0179 a0002c0002t0008g0205 others(8): Show |
11 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-22477dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450179 | |||||||
| chr7:44450217 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-22514C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450217 | |||||||
| chr7:44450378 | A | G | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510-22675T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450378 | |||||||
| chr7:44450422 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-22719G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450422 | |||||||
| chr7:44450467 | T | C | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-22764A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450467 | |||||||
| chr7:44450468 | G | A | 3 | a0002c0002t0021g0217 a0002c0005t0012g0235 a0002c0005t0012g0236 |
3 | HG02922.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510-22765C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450468 | |||||||
| chr7:44450557 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-22854A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450557 | |||||||
| chr7:44450573 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.510-22870G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450573 | |||||||
| chr7:44450652 | A | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-22949T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450652 | |||||||
| chr7:44450796 | A | T | 8 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-23093T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450796 | |||||||
| chr7:44451031 | C | T | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.510-23328G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451031 | |||||||
| chr7:44451509 | T | C | 3 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0211 |
3 | HG02683.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.510-23806A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451509 | |||||||
| chr7:44451571 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG02280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-23868C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451571 | |||||||
| chr7:44451604 | G | A | 2 | a0003c0003t0005g0218 a0003c0003t0005g0219 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-23901C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451604 | |||||||
| chr7:44451668 | T | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-23965A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451668 | |||||||
| chr7:44452036 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.510-24333C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452036 | |||||||
| chr7:44452041 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-24338C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452041 | |||||||
| chr7:44452058 | T | G | 2 | a0003c0003t0005g0222 a0003c0003t0005g0223 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.510-24355A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452058 | |||||||
| chr7:44452264 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.510-24561C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452264 | |||||||
| chr7:44452454 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-24751G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452454 | |||||||
| chr7:44452699 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02280.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-24996A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452699 | |||||||
| chr7:44452729 | G | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-25026C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452729 | |||||||
| chr7:44452824 | A | C | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-25121T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452824 | |||||||
| chr7:44453029 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.510-25326A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453029 | |||||||
| chr7:44453075 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-25372C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453075 | |||||||
| chr7:44453081 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-25378C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453081 | |||||||
| chr7:44453168 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-25465G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453168 | |||||||
| chr7:44453233 | A | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-25530T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453233 | |||||||
| chr7:44453349 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-25646A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453349 | |||||||
| chr7:44453360 | T | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-25657A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453360 | |||||||
| chr7:44453406 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-25703T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453406 | |||||||
| chr7:44453770 | G | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-26067C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453770 | |||||||
| chr7:44453813 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-26110C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453813 | |||||||
| chr7:44454164 | G | A | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.510-26461C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454164 | |||||||
| chr7:44454271 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.510-26568C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454271 | |||||||
| chr7:44454317 | T | C | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-26614A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454317 | |||||||
| chr7:44454651 | G | A | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510-26948C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454651 | |||||||
| chr7:44454772 | A | T | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-27069T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454772 | |||||||
| chr7:44454773 | T | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-27070A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454773 | |||||||
| chr7:44454847 | T | C | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-27144A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454847 | |||||||
| chr7:44454936 | A | AAC | 14 | a0001c0001t0001g0045 a0001c0001t0001g0081 a0001c0001t0001g0109 others(11): Show |
14 | HG00642.hp2 HG01257.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-27235_510-2723 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | |||||||
| chr7:44454936 | A | AACAC | 4 | a0002c0002t0007g0197 a0002c0002t0007g0198 a0002c0002t0010g0193 others(1): Show |
4 | HG00741.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-27237_510-2723 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | |||||||
| chr7:44454936 | A | AACACAC | 3 | a0002c0002t0007g0196 a0002c0005t0012g0235 a0002c0005t0012g0236 |
3 | HG02922.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510-27239_510-2723 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | |||||||
| chr7:44454936 | A | AC | 2 | a0001c0001t0002g0057 a0001c0001t0016g0002 |
2 | HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.510-27234_510-2723 others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | |||||||
| chr7:44454936 | AAC | A | 13 | a0001c0001t0003g0042 a0002c0002t0004g0207 a0002c0002t0004g0208 others(10): Show |
13 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.510-27235_510-2723 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | |||||||
| chr7:44455216 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-27513A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455216 | |||||||
| chr7:44455294 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.510-27591G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455294 | |||||||
| chr7:44455333 | G | A | 1 | a0001c0001t0033g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510-27630C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455333 | |||||||
| chr7:44455345 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-27642T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455345 | |||||||
| chr7:44455690 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-27987T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455690 | |||||||
| chr7:44455941 | G | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-28238C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455941 | |||||||
| chr7:44455983 | G | A | 1 | a0002c0002t0022g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.510-28280C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455983 | |||||||
| chr7:44456000 | T | TG | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-28298dupC | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456000 | |||||||
| chr7:44456020 | C | G | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-28317G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456020 | |||||||
| chr7:44456025 | C | CA | 49 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0044 others(46): Show |
49 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.510-28323dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | |||||||
| chr7:44456025 | C | CAA | 12 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0002c0002t0004g0207 others(9): Show |
12 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-28324_510-2832 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | |||||||
| chr7:44456025 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0074 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-28334_510-2832 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | |||||||
| chr7:44456036 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.510-28333T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456036 | |||||||
| chr7:44456037 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-28334T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456037 | |||||||
| chr7:44456038 | AAAAAAAA others(6): Show |
A | 17 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-28348_510-2833 others(17): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456038 | |||||||
| chr7:44456039 | AAAAAAAA others(5): Show |
A | 1 | a0003c0003t0009g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510-28348_510-2833 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456039 | |||||||
| chr7:44456041 | A | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-28338T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456041 | |||||||
| chr7:44456051 | C | A | 4 | a0001c0001t0001g0145 a0002c0002t0007g0196 a0002c0002t0007g0197 others(1): Show |
4 | HG01106.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-28348G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456051 | |||||||
| chr7:44456063 | C | CAACAAT | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.510-28366_510-2836 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456063 | |||||||
| chr7:44456136 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510-28433G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456136 | |||||||
| chr7:44456164 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510-28461G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456164 | |||||||
| chr7:44456352 | T | C | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+28616A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456352 | |||||||
| chr7:44456406 | T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+28562A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456406 | |||||||
| chr7:44456564 | T | C | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+28404A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456564 | |||||||
| chr7:44456608 | T | C | 8 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(5): Show |
8 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+28360A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456608 | |||||||
| chr7:44456650 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509+28318C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456650 | |||||||
| chr7:44456754 | T | TA | 16 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.509+28213dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456754 | |||||||
| chr7:44456969 | T | C | 26 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+27999A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456969 | |||||||
| chr7:44457027 | T | TA | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+27940dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457027 | |||||||
| chr7:44457039 | A | C | 1 | a0001c0001t0003g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.509+27929T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457039 | |||||||
| chr7:44457249 | C | T | 26 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+27719G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457249 | |||||||
| chr7:44457299 | T | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+27669A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457299 | |||||||
| chr7:44457461 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.509+27507T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457461 | |||||||
| chr7:44457616 | T | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+27352A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457616 | |||||||
| chr7:44457650 | C | T | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.509+27318G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457650 | |||||||
| chr7:44457662 | G | C | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.509+27306C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457662 | |||||||
| chr7:44457863 | T | C | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+27105A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457863 | |||||||
| chr7:44458149 | C | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509+26819G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458149 | |||||||
| chr7:44458476 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+26492T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458476 | |||||||
| chr7:44458619 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+26349A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458619 | |||||||
| chr7:44458659 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+26309C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458659 | |||||||
| chr7:44458663 | G | GA | 43 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.509+26304dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458663 | |||||||
| chr7:44458690 | T | C | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.509+26278A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458690 | |||||||
| chr7:44458903 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+26065T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458903 | |||||||
| chr7:44458936 | C | CTG | 29 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0038 others(26): Show |
29 | HG00544.hp1 HG00642.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+26030_509+2603 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTG | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(42): Show |
45 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.509+26028_509+2603 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTG | 32 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0027 others(29): Show |
32 | HG00642.hp2 HG00741.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.509+26026_509+2603 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTGT others(1): Show |
24 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0050 others(21): Show |
24 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+26024_509+2603 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTGT others(3): Show |
14 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0085 others(11): Show |
14 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+26022_509+2603 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTGT others(5): Show |
7 | a0001c0001t0001g0055 a0001c0001t0001g0079 a0001c0001t0001g0084 others(4): Show |
7 | HG00735.hp1 HG01175.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+26020_509+2603 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0134 |
2 | HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.509+26018_509+2603 others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+26016_509+2603 others(20): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTG | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0002g0046 others(5): Show |
8 | HG00639.hp2 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+26030_509+2603 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTG | C | 8 | a0002c0002t0008g0205 a0002c0002t0008g0206 a0002c0002t0020g0203 others(5): Show |
8 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+26028_509+2603 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTG | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0003g0043 others(10): Show |
14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+26026_509+2603 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTGT others(1): Show |
C | 3 | a0002c0002t0010g0193 a0002c0002t0010g0201 a0002c0002t0023g0209 |
3 | HG00741.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509+26024_509+2603 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTGT others(3): Show |
C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+26022_509+2603 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTGT others(7): Show |
C | 4 | a0002c0002t0004g0213 a0002c0002t0004g0216 a0002c0005t0012g0235 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+26018_509+2603 others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTGT others(9): Show |
C | 5 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0211 others(2): Show |
5 | HG01109.hp2 HG02683.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+26016_509+2603 others(20): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44458936 | CTGTGTGT others(13): Show |
C | 2 | a0002c0002t0004g0210 a0002c0002t0004g0212 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.509+26012_509+2603 others(24): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | |||||||
| chr7:44459091 | T | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+25877A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459091 | |||||||
| chr7:44459162 | T | A | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+25806A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459162 | |||||||
| chr7:44459178 | G | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+25790C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459178 | |||||||
| chr7:44459203 | CT | C | 12 | a0001c0001t0001g0147 a0002c0002t0004g0214 a0002c0002t0007g0196 others(9): Show |
12 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.509+25764delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459203 | |||||||
| chr7:44459440 | G | A | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+25528C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459440 | |||||||
| chr7:44459472 | G | T | 1 | a0003c0003t0019g0232 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+25496C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459472 | |||||||
| chr7:44459703 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.509+25265G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459703 | |||||||
| chr7:44460042 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+24926T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460042 | |||||||
| chr7:44460131 | C | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+24837G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460131 | |||||||
| chr7:44460237 | G | A | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+24731C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460237 | |||||||
| chr7:44460722 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0155 |
2 | NA18612.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.509+24246T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460722 | |||||||
| chr7:44460803 | T | C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
30 | HG00609.hp1 HG01952.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.509+24165A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460803 | |||||||
| chr7:44460821 | T | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+24147A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460821 | |||||||
| chr7:44461026 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+23942G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461026 | |||||||
| chr7:44461056 | C | T | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+23912G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461056 | |||||||
| chr7:44461274 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0140 |
2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.509+23694A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461274 | |||||||
| chr7:44461406 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+23562C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461406 | |||||||
| chr7:44461525 | G | C | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+23443C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461525 | |||||||
| chr7:44461670 | T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+23298A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461670 | |||||||
| chr7:44461748 | C | T | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+23220G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461748 | |||||||
| chr7:44461790 | G | T | 11 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+23178C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461790 | |||||||
| chr7:44462067 | A | C | 1 | a0001c0001t0034g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.509+22901T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462067 | |||||||
| chr7:44462141 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+22827C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462141 | |||||||
| chr7:44462170 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG02015.hp2 HG02071.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+22798A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462170 | |||||||
| chr7:44462297 | T | C | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+22671A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462297 | |||||||
| chr7:44462387 | A | G | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+22581T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462387 | |||||||
| chr7:44462521 | C | T | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+22447G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462521 | |||||||
| chr7:44462587 | C | T | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+22381G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462587 | |||||||
| chr7:44462678 | T | A | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+22290A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462678 | |||||||
| chr7:44462816 | A | G | 44 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.509+22152T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462816 | |||||||
| chr7:44462864 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.509+22104A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462864 | |||||||
| chr7:44462866 | T | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+22102A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462866 | |||||||
| chr7:44462945 | C | CTG | 7 | a0001c0001t0001g0061 a0001c0001t0001g0145 a0001c0001t0002g0069 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+22021_509+2202 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | C | CTGTG | 6 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(3): Show |
6 | HG00544.hp1 HG02071.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+22019_509+2202 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | C | CTGTGTG | 2 | a0001c0001t0002g0057 a0001c0001t0002g0178 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.509+22017_509+2202 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | CTG | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0131 others(14): Show |
17 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+22021_509+2202 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | CTGTG | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0027 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.509+22019_509+2202 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | CTGTGTG | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.509+22017_509+2202 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | CTGTGTGT others(1): Show |
C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0092 others(9): Show |
13 | HG00673.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+22015_509+2202 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462945 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0119 a0003c0003t0009g0220 a0003c0003t0009g0228 |
3 | HG01358.hp2 HG03471.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.509+22013_509+2202 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | |||||||
| chr7:44462953 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+22015C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462953 | |||||||
| chr7:44462979 | GTGTGTGT others(5): Show |
G | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462979 | |||||||
| chr7:44462983 | GTGTGTGT others(1): Show |
G | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462983 | |||||||
| chr7:44462985 | GTGTGTA | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0152 others(1): Show |
4 | HG00544.hp2 HG02155.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+21977_509+2198 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462985 | |||||||
| chr7:44462987 | GTGTA | G | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462987 | |||||||
| chr7:44463026 | G | C | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+21942C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463026 | |||||||
| chr7:44463172 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
89 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.509+21796T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463172 | |||||||
| chr7:44463213 | A | G | 1 | a0002c0002t0004g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.509+21755T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463213 | |||||||
| chr7:44463336 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.509+21632C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463336 | |||||||
| chr7:44463356 | C | T | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+21612G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463356 | |||||||
| chr7:44463472 | G | C | 1 | a0001c0001t0003g0175 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509+21496C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463472 | |||||||
| chr7:44463605 | C | G | 2 | a0002c0002t0004g0214 a0002c0002t0022g0215 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.509+21363G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463605 | |||||||
| chr7:44463855 | T | C | 8 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+21113A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463855 | |||||||
| chr7:44463957 | T | C | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+21011A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463957 | |||||||
| chr7:44463970 | T | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+20998A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463970 | |||||||
| chr7:44463987 | G | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+20981C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463987 | |||||||
| chr7:44464077 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509+20891C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464077 | |||||||
| chr7:44464213 | C | CA | 8 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01978.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+20754dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464213 | |||||||
| chr7:44464213 | CA | C | 9 | a0001c0001t0002g0183 a0002c0002t0007g0196 a0002c0002t0007g0197 others(6): Show |
9 | HG00741.hp2 HG01081.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+20754delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464213 | |||||||
| chr7:44464230 | GA | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+20737delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464230 | |||||||
| chr7:44464388 | A | G | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+20580T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464388 | |||||||
| chr7:44464513 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+20455C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464513 | |||||||
| chr7:44464578 | T | C | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+20390A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464578 | |||||||
| chr7:44464674 | G | A | 1 | a0002c0002t0022g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509+20294C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464674 | |||||||
| chr7:44465066 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.509+19902G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465066 | |||||||
| chr7:44465111 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
87 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.509+19857G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465111 | |||||||
| chr7:44465639 | T | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+19329A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465639 | |||||||
| chr7:44465660 | C | T | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+19308G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465660 | |||||||
| chr7:44465792 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+19176G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465792 | |||||||
| chr7:44465893 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+19075C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465893 | |||||||
| chr7:44466129 | C | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0044 |
2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.509+18839G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466129 | |||||||
| chr7:44466512 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+18456A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466512 | |||||||
| chr7:44466693 | C | T | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+18275G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466693 | |||||||
| chr7:44466805 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+18163C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466805 | |||||||
| chr7:44466882 | G | A | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.509+18086C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466882 | |||||||
| chr7:44467184 | GAT | G | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+17782_509+1778 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467184 | |||||||
| chr7:44467394 | C | T | 7 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(4): Show |
7 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+17574G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467394 | |||||||
| chr7:44467543 | G | A | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+17425C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467543 | |||||||
| chr7:44467638 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509+17330G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467638 | |||||||
| chr7:44467817 | TA | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0002c0002t0021g0217 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.509+17150delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467817 | |||||||
| chr7:44467827 | AAAAAG | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(37): Show |
40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+17136_509+1714 others(9): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467827 | |||||||
| chr7:44467855 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0046 |
2 | HG01981.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.509+17113C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467855 | |||||||
| chr7:44467866 | C | T | 3 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0211 |
3 | HG02683.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.509+17102G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467866 | |||||||
| chr7:44467867 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+17101C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467867 | |||||||
| chr7:44468033 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02698.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.509+16935C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468033 | |||||||
| chr7:44468079 | G | A | 2 | a0002c0002t0004g0213 a0002c0002t0004g0216 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.509+16889C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468079 | |||||||
| chr7:44468284 | C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+16684G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468284 | |||||||
| chr7:44468285 | G | A | 9 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(6): Show |
9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+16683C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468285 | |||||||
| chr7:44468289 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+16679G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468289 | |||||||
| chr7:44468349 | C | CA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00544.hp2 HG00639.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.509+16618dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | |||||||
| chr7:44468349 | CA | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0102 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+16618delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | |||||||
| chr7:44468349 | CAA | C | 12 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(9): Show |
12 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+16617_509+1661 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | |||||||
| chr7:44468365 | A | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+16603T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468365 | |||||||
| chr7:44468366 | A | G | 10 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG02155.hp1 HG04184.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+16602T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468366 | |||||||
| chr7:44468410 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+16558A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468410 | |||||||
| chr7:44468809 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.509+16159C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468809 | |||||||
| chr7:44469115 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.509+15853G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | C | CA | 46 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(43): Show |
46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.509+15852dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | C | CAA | 9 | a0001c0001t0001g0049 a0001c0001t0001g0092 a0001c0001t0001g0112 others(6): Show |
9 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+15851_509+1585 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | CA | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0118 a0001c0001t0001g0147 others(2): Show |
5 | HG01081.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+15852delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | CAA | C | 8 | a0003c0003t0006g0227 a0003c0003t0006g0229 a0003c0003t0006g0231 others(5): Show |
8 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+15851_509+1585 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | CAAAA | C | 9 | a0002c0002t0004g0214 a0002c0002t0022g0215 a0003c0003t0005g0218 others(6): Show |
9 | HG00099.hp2 HG00280.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+15849_509+1585 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469115 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0051 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.509+15843_509+1585 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | |||||||
| chr7:44469193 | T | A | 1 | a0003c0003t0019g0230 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.509+15775A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469193 | |||||||
| chr7:44469224 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.509+15744C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469224 | |||||||
| chr7:44469438 | G | A | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+15530C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469438 | |||||||
| chr7:44469520 | T | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+15448A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469520 | |||||||
| chr7:44469525 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.509+15443C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469525 | |||||||
| chr7:44469531 | G | A | 39 | a0002c0002t0004g0207 a0002c0002t0004g0208 a0002c0002t0004g0210 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+15437C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469531 | |||||||
| chr7:44469702 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.509+15266T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469702 | |||||||
| chr7:44470100 | G | T | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+14868C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470100 | |||||||
| chr7:44470110 | T | C | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.509+14858A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470110 | |||||||
| chr7:44470117 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+14851C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470117 | |||||||
| chr7:44470144 | T | C | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+14824A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470144 | |||||||
| chr7:44470204 | T | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+14764A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470204 | |||||||
| chr7:44470425 | C | T | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.509+14543G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470425 | |||||||
| chr7:44470476 | A | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+14492T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470476 | |||||||
| chr7:44470477 | T | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+14491A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470477 | |||||||
| chr7:44471238 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+13730C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471238 | |||||||
| chr7:44471612 | A | C | 1 | a0001c0001t0029g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+13356T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471612 | |||||||
| chr7:44471737 | C | T | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+13231G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471737 | |||||||
| chr7:44471862 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+13106G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471862 | |||||||
| chr7:44472046 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+12922G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472046 | |||||||
| chr7:44472046 | C | T | 1 | a0001c0001t0037g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509+12922G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472046 | |||||||
| chr7:44472556 | A | G | 13 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(10): Show |
13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+12412T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472556 | |||||||
| chr7:44472644 | C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+12324G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472644 | |||||||
| chr7:44473154 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.509+11814G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473154 | |||||||
| chr7:44473157 | A | G | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+11811T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473157 | |||||||
| chr7:44473392 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+11576T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473392 | |||||||
| chr7:44473535 | T | C | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+11433A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473535 | |||||||
| chr7:44473749 | A | G | 10 | a0001c0001t0001g0079 a0002c0002t0004g0207 a0002c0002t0004g0208 others(7): Show |
10 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.509+11219T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473749 | |||||||
| chr7:44473845 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+11123T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473845 | |||||||
| chr7:44473959 | C | G | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+11009G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473959 | |||||||
| chr7:44474083 | G | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+10885C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474083 | |||||||
| chr7:44474182 | C | CA | 49 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(46): Show |
49 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+10785dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474182 | |||||||
| chr7:44474182 | CAA | C | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+10784_509+1078 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474182 | |||||||
| chr7:44474336 | A | G | 3 | a0001c0001t0002g0051 a0001c0001t0015g0052 a0001c0001t0015g0078 |
3 | HG00323.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.509+10632T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474336 | |||||||
| chr7:44474387 | A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+10581T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474387 | |||||||
| chr7:44474413 | T | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+10555A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474413 | |||||||
| chr7:44474828 | T | C | 2 | a0002c0002t0004g0214 a0002c0002t0022g0215 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.509+10140A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474828 | |||||||
| chr7:44474914 | C | A | 1 | a0003c0003t0005g0225 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.509+10054G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474914 | |||||||
| chr7:44474993 | C | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+9975G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474993 | |||||||
| chr7:44475033 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.509+9935T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475033 | |||||||
| chr7:44475112 | C | CT | 13 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0002g0183 others(10): Show |
13 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+9855dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | |||||||
| chr7:44475112 | C | CTT | 8 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+9854_509+9855d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | |||||||
| chr7:44475112 | CT | C | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0003g0176 others(2): Show |
5 | HG01070.hp1 HG01070.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+9855delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | |||||||
| chr7:44475143 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0167 |
2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.509+9825C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475143 | |||||||
| chr7:44475211 | A | G | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+9757T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475211 | |||||||
| chr7:44475316 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
8 | HG00544.hp2 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+9652A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475316 | |||||||
| chr7:44475668 | G | C | 2 | a0002c0002t0011g0194 a0002c0002t0011g0195 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+9300C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475668 | |||||||
| chr7:44475717 | A | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.509+9251T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475717 | |||||||
| chr7:44476057 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+8911C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476057 | |||||||
| chr7:44476494 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.509+8474G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476494 | |||||||
| chr7:44476528 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+8440C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476528 | |||||||
| chr7:44476622 | C | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
8 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+8346G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476622 | |||||||
| chr7:44476794 | C | T | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+8174G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476794 | |||||||
| chr7:44476816 | G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+8152C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476816 | |||||||
| chr7:44476945 | G | T | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+8023C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476945 | |||||||
| chr7:44476954 | C | CTGA | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+8011_509+8013d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476954 | |||||||
| chr7:44477025 | AT | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+7942delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477025 | |||||||
| chr7:44477046 | G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+7922C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477046 | |||||||
| chr7:44477298 | T | A | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+7670A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477298 | |||||||
| chr7:44477611 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+7357C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477611 | |||||||
| chr7:44477822 | C | CT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(18): Show |
21 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.509+7145dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477822 | |||||||
| chr7:44477822 | CT | C | 27 | a0001c0001t0001g0134 a0001c0001t0001g0168 a0001c0001t0003g0042 others(24): Show |
27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.509+7145delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477822 | |||||||
| chr7:44477830 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.509+7138A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477830 | |||||||
| chr7:44477895 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.509+7073T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477895 | |||||||
| chr7:44478098 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+6870A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478098 | |||||||
| chr7:44478115 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+6853A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478115 | |||||||
| chr7:44478231 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.509+6737G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478231 | |||||||
| chr7:44478247 | A | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+6721T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478247 | |||||||
| chr7:44478300 | C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+6668G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478300 | |||||||
| chr7:44478454 | A | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+6514T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478454 | |||||||
| chr7:44478467 | C | T | 2 | a0003c0003t0005g0218 a0003c0003t0005g0219 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.509+6501G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478467 | |||||||
| chr7:44478714 | A | G | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+6254T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478714 | |||||||
| chr7:44478781 | A | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+6187T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478781 | |||||||
| chr7:44478945 | T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+6023A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478945 | |||||||
| chr7:44479049 | C | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+5919G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479049 | |||||||
| chr7:44479086 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+5882C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479086 | |||||||
| chr7:44479334 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.509+5634G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479334 | |||||||
| chr7:44479472 | A | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(10): Show |
13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+5496T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479472 | |||||||
| chr7:44479477 | A | G | 13 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(10): Show |
13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+5491T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479477 | |||||||
| chr7:44479538 | T | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+5430A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479538 | |||||||
| chr7:44479650 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+5318C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479650 | |||||||
| chr7:44479670 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.509+5298A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479670 | |||||||
| chr7:44480024 | G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+4944C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480024 | |||||||
| chr7:44480635 | A | C | 28 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.509+4333T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480635 | |||||||
| chr7:44480659 | T | A | 25 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+4309A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480659 | |||||||
| chr7:44480712 | C | T | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+4256G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480712 | |||||||
| chr7:44480738 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.509+4230A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480738 | |||||||
| chr7:44480920 | C | G | 3 | a0002c0002t0008g0204 a0002c0002t0008g0205 a0002c0002t0008g0206 |
3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+4048G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480920 | |||||||
| chr7:44480941 | C | CA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
40 | HG00438.hp2 HG00544.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+4026dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | |||||||
| chr7:44480941 | C | CAAAAAAA others(8): Show |
1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+4012_509+4026d others(17): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | |||||||
| chr7:44480941 | C | CAAAAAAA others(10): Show |
1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+4010_509+4026d others(19): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | |||||||
| chr7:44480941 | CA | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(9): Show |
12 | HG00639.hp1 HG00741.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.509+4026delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | |||||||
| chr7:44480941 | CAAAA | C | 14 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+4023_509+4026d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | |||||||
| chr7:44480979 | G | GA | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0172 others(3): Show |
6 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+3988dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480979 | |||||||
| chr7:44481256 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.509+3712T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481256 | |||||||
| chr7:44481412 | T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+3556A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481412 | |||||||
| chr7:44481578 | A | G | 1 | a0002c0002t0020g0203 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.509+3390T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481578 | |||||||
| chr7:44481602 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509+3366G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481602 | |||||||
| chr7:44481921 | A | G | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+3047T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481921 | |||||||
| chr7:44482222 | G | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+2746C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482222 | |||||||
| chr7:44482258 | G | C | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+2710C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482258 | |||||||
| chr7:44482849 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509+2119A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482849 | |||||||
| chr7:44483007 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+1961A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483007 | |||||||
| chr7:44483018 | T | C | 18 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+1950A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483018 | |||||||
| chr7:44483233 | G | C | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+1735C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483233 | |||||||
| chr7:44483475 | C | T | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1493G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483475 | |||||||
| chr7:44483670 | C | T | 2 | a0002c0002t0007g0196 a0002c0002t0007g0197 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+1298G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483670 | |||||||
| chr7:44483876 | T | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(37): Show |
40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+1092A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483876 | |||||||
| chr7:44483914 | G | A | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+1054C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483914 | |||||||
| chr7:44484052 | C | G | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+916G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484052 | |||||||
| chr7:44484114 | G | A | 1 | a0001c0001t0033g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+854C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484114 | |||||||
| chr7:44484518 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0003g0029 others(4): Show |
7 | HG01993.hp2 HG02165.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+450T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484518 | |||||||
| chr7:44484601 | C | G | 20 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0002c0002t0021g0217 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.509+367G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484601 | |||||||
| chr7:44484754 | C | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+214G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484754 | |||||||
| chr7:44484854 | A | C | 1 | a0001c0001t0035g0026 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.509+114T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484854 | |||||||
| chr7:44484939 | G | A | 3 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+29C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484939 | |||||||
| chr7:44484952 | A | C | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+16T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484952 | |||||||
| chr7:44485302 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193-18A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485302 | |||||||
| chr7:44485589 | T | C | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-305A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485589 | |||||||
| chr7:44485775 | C | T | 27 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0002c0002t0007g0196 others(24): Show |
27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.193-491G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485775 | |||||||
| chr7:44485798 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-514C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485798 | |||||||
| chr7:44485802 | G | A | 2 | a0001c0001t0003g0175 a0001c0001t0003g0176 |
2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.193-518C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485802 | |||||||
| chr7:44486034 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193-750G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486034 | |||||||
| chr7:44486035 | G | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.193-751C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486035 | |||||||
| chr7:44486091 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.193-807C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486091 | |||||||
| chr7:44486204 | C | G | 20 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0002c0002t0021g0217 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-920G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486204 | |||||||
| chr7:44486508 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.193-1224A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486508 | |||||||
| chr7:44486521 | GA | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(8): Show |
11 | HG01952.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-1238delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486521 | |||||||
| chr7:44486766 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.193-1482C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486766 | |||||||
| chr7:44486839 | C | T | 2 | a0002c0002t0010g0193 a0002c0002t0010g0201 |
2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.193-1555G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486839 | |||||||
| chr7:44486857 | C | G | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-1573G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486857 | |||||||
| chr7:44486876 | T | C | 20 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0002c0002t0021g0217 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-1592A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486876 | |||||||
| chr7:44487331 | G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-2047C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487331 | |||||||
| chr7:44487460 | G | GA | 22 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0182 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-2177dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487460 | |||||||
| chr7:44487559 | C | T | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.193-2275G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487559 | |||||||
| chr7:44487744 | A | G | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-2460T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487744 | |||||||
| chr7:44487756 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-2472C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487756 | |||||||
| chr7:44487769 | G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-2485C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487769 | |||||||
| chr7:44487818 | G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.193-2534C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487818 | |||||||
| chr7:44487904 | G | A | 2 | a0002c0005t0012g0235 a0002c0005t0012g0236 |
2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.192+2505C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487904 | |||||||
| chr7:44487909 | C | T | 1 | a0001c0001t0014g0012 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.192+2500G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487909 | |||||||
| chr7:44488086 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.192+2323A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488086 | |||||||
| chr7:44488318 | G | A | 2 | a0002c0002t0021g0217 a0002c0002t0040g0237 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.192+2091C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488318 | |||||||
| chr7:44488333 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.192+2076A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488333 | |||||||
| chr7:44488338 | GA | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0191 a0001c0001t0002g0010 others(5): Show |
8 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+2070delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488338 | |||||||
| chr7:44488338 | GAA | G | 20 | a0002c0002t0010g0193 a0002c0002t0010g0201 a0002c0002t0021g0217 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+2069_192+2070d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488338 | |||||||
| chr7:44488339 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.192+2070T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488339 | |||||||
| chr7:44488354 | A | G | 7 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+2055T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488354 | |||||||
| chr7:44488552 | TC | T | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.192+1856delG | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488552 | |||||||
| chr7:44488827 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.192+1582C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488827 | |||||||
| chr7:44488986 | T | G | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.192+1423A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488986 | |||||||
| chr7:44489103 | T | C | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192+1306A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489103 | |||||||
| chr7:44489124 | C | T | 2 | a0002c0002t0018g0199 a0002c0002t0018g0200 |
2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.192+1285G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489124 | |||||||
| chr7:44489236 | A | G | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192+1173T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489236 | |||||||
| chr7:44489390 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG02015.hp2 HG02071.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1019C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489390 | |||||||
| chr7:44489660 | T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+749A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489660 | |||||||
| chr7:44489670 | C | G | 5 | a0002c0002t0007g0196 a0002c0002t0007g0197 a0002c0002t0007g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+739G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489670 | |||||||
| chr7:44489675 | A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+734T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489675 | |||||||
| chr7:44489725 | T | TGTAA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.192+683_192+684ins others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489725 | |||||||
| chr7:44489799 | T | C | 1 | a0001c0001t0002g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.192+610A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489799 | |||||||
| chr7:44489852 | C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+557G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489852 | |||||||
| chr7:44490063 | G | A | 16 | a0003c0003t0005g0218 a0003c0003t0005g0219 a0003c0003t0005g0221 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.192+346C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490063 | |||||||
| chr7:44490080 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.192+329A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490080 | |||||||
| chr7:44490127 | G | A | 18 | a0002c0002t0021g0217 a0002c0002t0040g0237 a0003c0003t0005g0218 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+282C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490127 | |||||||
| chr7:44490130 | C | T | 1 | a0002c0002t0010g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.192+279G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490130 |