Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54820 |
|---|---|
| ensemblid | ENSG00000072864.16 |
| hgncid | 17619 |
| symbol | NDE1 |
| name | nudE neurodevelopment protein 1 |
| refseq_nuc | NM_017668.3 |
| refseq_prot | NP_060138.1 |
| ensembl_nuc | ENST00000396354.6 |
| ensembl_prot | ENSP00000379642.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 15650245 |
| end | 15726353 |
| strand | + |
| ver | v1.2 |
| region | chr16:15650245-15726353 |
| region5000 | chr16:15645245-15731353 |
| regionname0 | NDE1_chr16_15650245_15726353 |
| regionname5000 | NDE1_chr16_15645245_15731353 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 335 | 365 | 92 | 67 | 155 | 14 | 36 | 115 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0002 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0003 | 0/0 | 335 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1008 | 359 | 91 | 65 | 155 | 12 | 35 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| c0002 | 0/0 | 1008 | 5 | 0 | 2 | 0 | 2 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| c0003 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| c0004 | 0/0 | 1008 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| c0005 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2196 | 109 | 27 | 23 | 33 | 5 | 21 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0002 | 0/1 | 2196 | 92 | 11 | 21 | 44 | 6 | 9 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0003 | 0/0 | 2196 | 52 | 0 | 3 | 46 | 0 | 3 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0004 | 0/0 | 2206 | 19 | 18 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0005 | 0/0 | 2206 | 12 | 0 | 2 | 8 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0006 | 0/0 | 2196 | 11 | 7 | 0 | 4 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0007 | 0/0 | 2197 | 10 | 4 | 4 | 0 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0008 | 0/0 | 2196 | 10 | 9 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0009 | 0/0 | 2193 | 5 | 5 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0010 | 0/0 | 2196 | 5 | 0 | 4 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0011 | 0/0 | 2196 | 3 | 2 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0012 | 0/0 | 2196 | 3 | 0 | 3 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0013 | 0/0 | 2197 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0014 | 0/0 | 2196 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0015 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0016 | 0/0 | 2196 | 2 | 0 | 0 | 1 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0017 | 0/0 | 2197 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0018 | 0/0 | 2196 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0019 | 0/0 | 2196 | 2 | 0 | 2 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0020 | 0/0 | 2196 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0021 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0022 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0023 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0024 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0025 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0026 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0027 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0028 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0029 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0030 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0031 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0032 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0033 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0034 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0035 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0036 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0037 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| t0038 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1008 | 359 | 91 | 65 | 155 | 12 | 35 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0002 | 0/0 | 1008 | 5 | 0 | 2 | 0 | 2 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0003 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0002c0005 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0003c0004 | 0/0 | 1008 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3203 | 102 | 27 | 20 | 32 | 3 | 20 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0002 | 0/1 | 3203 | 92 | 11 | 21 | 44 | 6 | 9 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0003 | 0/0 | 3203 | 52 | 0 | 3 | 46 | 0 | 3 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0004 | 0/0 | 3213 | 19 | 18 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0005 | 0/0 | 3213 | 12 | 0 | 2 | 8 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0006 | 0/0 | 3203 | 10 | 6 | 0 | 4 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0007 | 0/0 | 3204 | 10 | 4 | 4 | 0 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0008 | 0/0 | 3203 | 10 | 9 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0009 | 0/0 | 3200 | 5 | 5 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0010 | 0/0 | 3203 | 5 | 0 | 4 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0011 | 0/0 | 3203 | 3 | 2 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0012 | 0/0 | 3203 | 3 | 0 | 3 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0013 | 0/0 | 3204 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0014 | 0/0 | 3203 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0015 | 0/0 | 3203 | 2 | 2 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0016 | 0/0 | 3203 | 2 | 0 | 0 | 1 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0017 | 0/0 | 3204 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0018 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0019 | 0/0 | 3203 | 2 | 0 | 2 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0020 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0021 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0022 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0023 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0024 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0025 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0026 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0027 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0028 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0029 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0030 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0031 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0032 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0033 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0034 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0035 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0036 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0037 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0001t0038 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0002t0001 | 0/0 | 3203 | 5 | 0 | 2 | 0 | 2 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0001c0003t0006 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0002c0005t0001 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| a0003c0004t0001 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | copy fasta | chr16 | 15645245 | 15731353 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0014g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0014g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0014g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0015g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0016g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0017g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0017g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0018g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0018g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0019g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0020g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0020g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0023g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0026g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0027g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0028g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0029g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0030g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0031g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0033g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0034g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0035g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0037g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0038g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0003t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0002c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0003c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0335 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0325 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0103 | EUR | FIN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00558 | hp1 | a0001 | c0001 | t0013 | g0063 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0101 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0102 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0326 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0206 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0153 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01109 | hp1 | a0001 | c0001 | t0012 | g0318 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0362 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01167 | hp2 | a0001 | c0001 | t0019 | g0042 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0323 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01169 | hp1 | a0001 | c0001 | t0019 | g0043 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0324 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01243 | hp2 | a0001 | c0001 | t0036 | g0046 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0328 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01257 | hp2 | a0001 | c0001 | t0012 | g0312 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0313 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0124 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01433 | hp2 | a0001 | c0001 | t0034 | g0077 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01496 | hp2 | a0001 | c0001 | t0011 | g0005 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0332 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0165 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0333 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0353 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01952 | hp2 | a0001 | c0001 | t0035 | g0209 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0014 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0356 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02055 | hp2 | a0001 | c0001 | t0030 | g0311 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0355 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02155 | hp2 | a0001 | c0001 | t0020 | g0056 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02280 | hp1 | a0001 | c0001 | t0031 | g0017 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0349 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0358 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0359 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02630 | hp2 | a0001 | c0001 | t0024 | g0185 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0113 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02647 | hp2 | a0001 | c0001 | t0033 | g0296 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0357 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0348 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02818 | hp1 | a0001 | c0001 | t0032 | g0019 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0351 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0350 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0215 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0354 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0360 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03491 | hp2 | a0001 | c0001 | t0016 | g0015 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03516 | hp1 | a0001 | c0001 | t0029 | g0007 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0327 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0281 | EAS | CHB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18944 | hp1 | a0001 | c0001 | t0026 | g0116 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18945 | hp1 | a0001 | c0001 | t0037 | g0088 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18948 | hp2 | a0002 | c0005 | t0001 | g0045 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18950 | hp2 | a0001 | c0001 | t0028 | g0239 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18952 | hp2 | a0001 | c0001 | t0014 | g0344 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18964 | hp1 | a0001 | c0001 | t0016 | g0016 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18965 | hp2 | a0001 | c0001 | t0017 | g0274 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18966 | hp1 | a0001 | c0001 | t0027 | g0280 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18970 | hp2 | a0001 | c0001 | t0038 | g0075 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18975 | hp1 | a0001 | c0001 | t0013 | g0031 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18979 | hp1 | a0001 | c0001 | t0020 | g0093 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18980 | hp2 | a0001 | c0001 | t0017 | g0225 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18982 | hp2 | a0001 | c0001 | t0018 | g0227 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19003 | hp1 | a0001 | c0001 | t0022 | g0132 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0080 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19009 | hp1 | a0001 | c0001 | t0021 | g0011 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0364 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19030 | hp2 | a0001 | c0001 | t0025 | g0006 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0214 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19062 | hp1 | a0001 | c0001 | t0018 | g0271 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19066 | hp1 | a0001 | c0001 | t0014 | g0345 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19077 | hp1 | a0001 | c0001 | t0014 | g0346 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ASW | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0154 | EUR | TSI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | TSI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | GIH | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0352 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0361 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0200 | REF | REF | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15667357
|
C | T | 1 | a0002 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.155C>T | p.Thr52Met | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/9 | 248/3203 | 155/1008 | 52/335 | chr16 | 15667357 | ||
| chr16:15696785
|
C | T | 1 | a0003 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.872C>T | p.Ser291Phe | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/9 | 965/3203 | 872/1008 | 291/335 | chr16 | 15696785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15691259
|
G | A | 1 | a0001c0003 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.639G>A | p.Pro213Pro | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/9 | 732/3203 | 639/1008 | 213/335 | chr16 | 15691259 | ||
| chr16:15696750
|
C | T | 1 | a0001c0002 | 5 | HG00738.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
synonymous_variant | LOW | c.837C>T | p.Tyr279Tyr | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/9 | 930/3203 | 837/1008 | 279/335 | chr16 | 15696750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15650251
|
G | A | 1 | a0001c0001t0015 | 2 | HG02970.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-87G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/9 | 14528 | chr16 | 15650251 | |||||
| chr16:15650255
|
C | T | 1 | a0001c0001t0038 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-83C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/9 | chr16 | 15650255 | ||||||
| chr16:15724284
|
A | C | 14 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(11): Show | 125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*33A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 33 | chr16 | 15724284 | |||||
| chr16:15724287
|
G | A | 1 | a0001c0001t0011 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*36G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 36 | chr16 | 15724287 | |||||
| chr16:15724368
|
G | A | 1 | a0001c0001t0019 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 117 | chr16 | 15724368 | |||||
| chr16:15724437
|
G | A | 1 | a0001c0001t0033 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 186 | chr16 | 15724437 | |||||
| chr16:15724453
|
G | A | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(16): Show | 182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*202G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 202 | chr16 | 15724453 | |||||
| chr16:15724489
|
C | G | 1 | a0001c0001t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 238 | chr16 | 15724489 | |||||
| chr16:15724635
|
C | T | 1 | a0001c0001t0031 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 384 | chr16 | 15724635 | |||||
| chr16:15724796
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0024others(1): Show | 33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*545G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 545 | chr16 | 15724796 | |||||
| chr16:15724902
|
G | T | 1 | a0001c0001t0030 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*651G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 651 | chr16 | 15724902 | |||||
| chr16:15724919
|
G | A | 1 | a0001c0001t0034 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 668 | chr16 | 15724919 | |||||
| chr16:15724985
|
A | G | 1 | a0001c0001t0010 | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*734A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 734 | chr16 | 15724985 | |||||
| chr16:15725114
|
C | G | 2 | a0001c0001t0016a0001c0001t0023 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*863C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 863 | chr16 | 15725114 | |||||
| chr16:15725134
|
T | TA | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0017others(1): Show | 16 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*898dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 899 | INFO_REALIGN_3_PRIME | chr16 | 15725134 | ||||
| chr16:15725134
|
TA | T | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0025 | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*898delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | INFO_REALIGN_3_PRIME | chr16 | 15725134 | ||||
| chr16:15725147
|
AAAC | A | 2 | a0001c0001t0009a0001c0001t0029 | 6 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*898_*900delACA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | INFO_REALIGN_3_PRIME | chr16 | 15725147 | ||||
| chr16:15725148
|
A | C | 1 | a0001c0001t0018 | 2 | NA18982.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*897A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 897 | chr16 | 15725148 | |||||
| chr16:15725149
|
A | G | 1 | a0001c0001t0030 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | chr16 | 15725149 | |||||
| chr16:15725150
|
C | A | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0010others(4): Show | 29 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*899C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 899 | chr16 | 15725150 | |||||
| chr16:15725162
|
C | A | 2 | a0001c0001t0026a0001c0001t0028 | 2 | NA18944.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*911C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 911 | chr16 | 15725162 | |||||
| chr16:15725164
|
A | C | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(4): Show | 38 | HG01109.hp1 HG01255.hp1 HG01257.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*913A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 913 | chr16 | 15725164 | |||||
| chr16:15725194
|
C | T | 1 | a0001c0001t0020 | 2 | HG02155.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*943C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 943 | chr16 | 15725194 | |||||
| chr16:15725198
|
G | A | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0024 | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 947 | chr16 | 15725198 | |||||
| chr16:15725352
|
G | A | 1 | a0001c0001t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1101 | chr16 | 15725352 | |||||
| chr16:15725459
|
T | TTGTCCCT others(4): Show |
4 | a0001c0001t0004a0001c0001t0005a0001c0001t0024others(1): Show | 33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insTCCC others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1211 | INFO_REALIGN_3_PRIME | chr16 | 15725459 | ||||
| chr16:15725471
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0024others(1): Show | 33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1220G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1220 | chr16 | 15725471 | |||||
| chr16:15725550
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0024others(1): Show | 33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1299A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1299 | chr16 | 15725550 | |||||
| chr16:15725556
|
C | A | 1 | a0001c0001t0022 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1305C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1305 | chr16 | 15725556 | |||||
| chr16:15725588
|
C | G | 1 | a0001c0001t0036 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1337C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1337 | chr16 | 15725588 | |||||
| chr16:15725640
|
G | A | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0024 | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1389G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1389 | chr16 | 15725640 | |||||
| chr16:15725746
|
T | C | 1 | a0001c0001t0023 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1495T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1495 | chr16 | 15725746 | |||||
| chr16:15725974
|
C | T | 2 | a0001c0001t0004a0001c0001t0024 | 20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1723C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1723 | chr16 | 15725974 | |||||
| chr16:15726013
|
T | C | 1 | a0001c0001t0035 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1762T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1762 | chr16 | 15726013 | |||||
| chr16:15726035
|
A | G | 2 | a0001c0001t0008a0001c0001t0015 | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1784A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1784 | chr16 | 15726035 | |||||
| chr16:15726041
|
T | C | 1 | a0001c0001t0038 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1790 | chr16 | 15726041 | |||||
| chr16:15726101
|
G | A | 1 | a0001c0001t0014 | 3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1850G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1850 | chr16 | 15726101 | |||||
| chr16:15726341
|
T | C | 2 | a0001c0001t0011a0001c0001t0029 | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2090T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 2090 | chr16 | 15726341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15650298
|
A | G | 1 | a0001c0001t0003g0365 | 1 | NA18960.hp1 | splice_region_variant&intron_variant | LOW | c.-44+4A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650298 | ||||||
| chr16:15650317
|
C | T | 2 | a0001c0001t0002g0363a0001c0001t0002g0364 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-44+23C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650317 | ||||||
| chr16:15650392
|
C | T | 15 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(12): Show | 15 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+98C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650392 | ||||||
| chr16:15650414
|
G | C | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+120G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650414 | ||||||
| chr16:15650432
|
T | C | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+138T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650432 | ||||||
| chr16:15650472
|
T | C | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+178T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650472 | ||||||
| chr16:15650566
|
G | A | 4 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(1): Show | 4 | NA18998.hp2 NA19009.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+272G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650566 | ||||||
| chr16:15650783
|
G | C | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+489G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650783 | ||||||
| chr16:15650890
|
C | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+596C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650890 | ||||||
| chr16:15651035
|
C | T | 7 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(4): Show | 7 | NA18952.hp2 NA18998.hp2 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+741C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651035 | ||||||
| chr16:15651060
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-44+766C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651060 | ||||||
| chr16:15651103
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-44+809C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651103 | ||||||
| chr16:15651334
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-44+1040G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651334 | ||||||
| chr16:15651430
|
G | GT | 21 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0341others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+1155dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15651430 | |||||
| chr16:15651430
|
GT | G | 60 | a0001c0001t0002g0107a0001c0001t0003g0001a0001c0001t0003g0008others(57): Show | 61 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-44+1155delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15651430 | |||||
| chr16:15651441
|
T | G | 10 | a0001c0001t0006g0018a0001c0001t0011g0003a0001c0001t0011g0004others(7): Show | 10 | HG01496.hp2 HG02040.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+1147T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651441 | ||||||
| chr16:15651441
|
T | TG | 15 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(12): Show | 15 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+1147_-44+1148i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651441 | ||||||
| chr16:15651442
|
T | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(15): Show | 18 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-44+1148T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651442 | ||||||
| chr16:15651443
|
T | TG | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1149_-44+1150i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651443 | ||||||
| chr16:15651444
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-44+1150T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651444 | ||||||
| chr16:15651446
|
T | G | 77 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-44+1152T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651446 | ||||||
| chr16:15651498
|
G | A | 4 | a0001c0001t0010g0101a0001c0001t0010g0102a0001c0001t0010g0103others(1): Show | 4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1204G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651498 | ||||||
| chr16:15651663
|
G | A | 7 | a0001c0001t0002g0154a0001c0001t0008g0348a0001c0001t0008g0349others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+1369G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651663 | ||||||
| chr16:15651673
|
C | A | 10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+1379C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651673 | ||||||
| chr16:15651719
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-44+1425C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651719 | ||||||
| chr16:15651729
|
C | T | 11 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0002g0316others(8): Show | 11 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+1435C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651729 | ||||||
| chr16:15651734
|
C | T | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-44+1440C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651734 | ||||||
| chr16:15651735
|
G | A | 4 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(1): Show | 4 | HG02040.hp1 HG02280.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1441G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651735 | ||||||
| chr16:15652376
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-44+2082C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652376 | ||||||
| chr16:15652618
|
A | C | 37 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0126others(34): Show | 38 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44+2324A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652618 | ||||||
| chr16:15652716
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+2422C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652716 | ||||||
| chr16:15652776
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+2482G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652776 | ||||||
| chr16:15652800
|
A | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+2506A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652800 | ||||||
| chr16:15652829
|
A | G | 2 | a0001c0001t0006g0018a0001c0001t0032g0019 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+2535A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652829 | ||||||
| chr16:15652856
|
G | C | 1 | a0001c0001t0006g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+2562G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652856 | ||||||
| chr16:15652912
|
C | T | 24 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(21): Show | 24 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-44+2618C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652912 | ||||||
| chr16:15652934
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-44+2640G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652934 | ||||||
| chr16:15652944
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-44+2650A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652944 | ||||||
| chr16:15653042
|
G | A | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-44+2748G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653042 | ||||||
| chr16:15653182
|
T | A | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+2888T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653182 | ||||||
| chr16:15653255
|
C | A | 205 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(202): Show | 205 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-44+2961C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653255 | ||||||
| chr16:15653577
|
G | A | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-44+3283G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653577 | ||||||
| chr16:15653781
|
G | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-44+3487G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653781 | ||||||
| chr16:15653797
|
G | A | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-44+3503G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653797 | ||||||
| chr16:15653812
|
C | G | 1 | a0001c0002t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-44+3518C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653812 | ||||||
| chr16:15654026
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-44+3732C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654026 | ||||||
| chr16:15654085
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0341 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-44+3791T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654085 | ||||||
| chr16:15654193
|
A | G | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+3899A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654193 | ||||||
| chr16:15654296
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-44+4002G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654296 | ||||||
| chr16:15654467
|
G | A | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+4173G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654467 | ||||||
| chr16:15654497
|
A | G | 64 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0008others(61): Show | 65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-44+4203A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654497 | ||||||
| chr16:15654523
|
G | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-44+4229G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654523 | ||||||
| chr16:15654602
|
CA | C | 241 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(238): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-44+4322delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15654602 | |||||
| chr16:15654615
|
AAC | A | 6 | a0001c0001t0006g0018a0001c0001t0011g0004a0001c0001t0011g0005others(3): Show | 6 | HG01496.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+4323_-44+4324d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15654615 | |||||
| chr16:15654616
|
A | C | 20 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+4322A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654616 | ||||||
| chr16:15654617
|
C | A | 20 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+4323C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654617 | ||||||
| chr16:15654618
|
A | C | 7 | a0001c0001t0006g0018a0001c0001t0011g0003a0001c0001t0011g0004others(4): Show | 7 | HG01496.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+4324A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654618 | ||||||
| chr16:15654622
|
A | C | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4328A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654622 | ||||||
| chr16:15654632
|
C | A | 2 | a0001c0001t0016g0015a0001c0001t0023g0014 | 2 | HG02040.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-44+4338C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654632 | ||||||
| chr16:15654763
|
A | G | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-44+4469A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654763 | ||||||
| chr16:15655006
|
C | T | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+4712C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655006 | ||||||
| chr16:15655042
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44+4748A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655042 | ||||||
| chr16:15655160
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-44+4866G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655160 | ||||||
| chr16:15655342
|
G | A | 2 | a0001c0001t0012g0312a0001c0001t0012g0313 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-44+5048G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655342 | ||||||
| chr16:15655425
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-44+5131G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655425 | ||||||
| chr16:15655429
|
G | C | 1 | a0001c0001t0002g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-44+5135G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655429 | ||||||
| chr16:15655442
|
G | T | 1 | a0001c0001t0007g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5148G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655442 | ||||||
| chr16:15655444
|
C | A | 1 | a0001c0001t0007g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5150C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655444 | ||||||
| chr16:15655450
|
C | A | 1 | a0001c0001t0007g0328 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5156C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655450 | ||||||
| chr16:15655571
|
T | C | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+5277T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655571 | ||||||
| chr16:15655631
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-44+5337A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655631 | ||||||
| chr16:15655662
|
A | G | 3 | a0001c0001t0003g0149a0001c0001t0003g0310a0001c0001t0003g0365 | 3 | NA18960.hp1 NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-44+5368A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655662 | ||||||
| chr16:15655791
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-44+5497A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655791 | ||||||
| chr16:15655946
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5652A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655946 | ||||||
| chr16:15655948
|
G | C | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5654G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655948 | ||||||
| chr16:15655977
|
T | G | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5683T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655977 | ||||||
| chr16:15655978
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5684G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655978 | ||||||
| chr16:15656064
|
G | T | 1 | a0001c0001t0006g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-44+5770G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656064 | ||||||
| chr16:15656109
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5815C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656109 | ||||||
| chr16:15656146
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5852A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656146 | ||||||
| chr16:15656162
|
G | A | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44+5868G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656162 | ||||||
| chr16:15656175
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5881G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656175 | ||||||
| chr16:15656297
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6003G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656297 | ||||||
| chr16:15656298
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6004A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656298 | ||||||
| chr16:15656299
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6005G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656299 | ||||||
| chr16:15656368
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6074A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656368 | ||||||
| chr16:15656370
|
A | C | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6076A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656370 | ||||||
| chr16:15656411
|
C | T | 2 | a0001c0001t0003g0036a0001c0001t0003g0037 | 2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-44+6117C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656411 | ||||||
| chr16:15656501
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6207T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656501 | ||||||
| chr16:15656519
|
T | TTTA | 39 | a0001c0001t0001g0212a0001c0001t0001g0309a0001c0001t0003g0001others(36): Show | 40 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-44+6247_-44+6249d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15656519 | |||||
| chr16:15656633
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-44+6339C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656633 | ||||||
| chr16:15656636
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-44+6342G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656636 | ||||||
| chr16:15656645
|
T | A | 61 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0126others(58): Show | 62 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.-44+6351T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656645 | ||||||
| chr16:15656697
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6403T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656697 | ||||||
| chr16:15656733
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6439G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656733 | ||||||
| chr16:15656734
|
T | G | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6440T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656734 | ||||||
| chr16:15656786
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-44+6492C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656786 | ||||||
| chr16:15656847
|
G | T | 1 | a0001c0002t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-44+6553G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656847 | ||||||
| chr16:15656857
|
G | A | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-44+6563G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656857 | ||||||
| chr16:15657103
|
T | G | 1 | a0001c0001t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6809T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657103 | ||||||
| chr16:15657165
|
T | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+6871T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657165 | ||||||
| chr16:15657176
|
C | T | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+6882C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657176 | ||||||
| chr16:15657222
|
C | T | 10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+6928C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657222 | ||||||
| chr16:15657388
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-44+7094C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657388 | ||||||
| chr16:15657500
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+7206T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657500 | ||||||
| chr16:15657597
|
T | C | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7139T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657597 | ||||||
| chr16:15657602
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7134A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657602 | ||||||
| chr16:15657603
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7133T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657603 | ||||||
| chr16:15657632
|
C | T | 1 | a0001c0001t0016g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-43-7104C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657632 | ||||||
| chr16:15657677
|
C | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG01934.hp2 HG02129.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-7059C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657677 | ||||||
| chr16:15657680
|
C | T | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-7056C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657680 | ||||||
| chr16:15657736
|
C | G | 134 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(131): Show | 134 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-43-7000C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657736 | ||||||
| chr16:15657791
|
G | A | 1 | a0001c0001t0004g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-6945G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657791 | ||||||
| chr16:15657803
|
T | C | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-6933T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657803 | ||||||
| chr16:15657815
|
T | C | 1 | a0001c0001t0020g0056 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-43-6921T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657815 | ||||||
| chr16:15657931
|
A | T | 1 | a0001c0001t0020g0093 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-43-6805A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657931 | ||||||
| chr16:15658055
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-6681G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658055 | ||||||
| chr16:15658117
|
G | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0281others(2): Show | 5 | HG00438.hp2 NA18747.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6619G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658117 | ||||||
| chr16:15658121
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43-6615C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658121 | ||||||
| chr16:15658225
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-43-6511C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658225 | ||||||
| chr16:15658603
|
T | G | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-6133T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658603 | ||||||
| chr16:15658758
|
G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0218a0001c0001t0002g0219others(4): Show | 8 | HG00280.hp1 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-5978G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658758 | ||||||
| chr16:15658759
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-43-5977C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658759 | ||||||
| chr16:15658803
|
C | T | 1 | a0001c0001t0007g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-43-5933C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658803 | ||||||
| chr16:15659066
|
G | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-5670G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659066 | ||||||
| chr16:15659307
|
CTA | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-43-5424_-43-5423d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659307 | |||||
| chr16:15659425
|
C | CT | 180 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(177): Show | 181 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-43-5282dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | |||||
| chr16:15659425
|
C | CTT | 36 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43-5283_-43-5282d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | |||||
| chr16:15659425
|
CT | C | 11 | a0001c0001t0001g0048a0001c0001t0002g0224a0001c0001t0002g0226others(8): Show | 11 | HG01517.hp1 HG02040.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-5282delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | |||||
| chr16:15659425
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0008g0348a0001c0001t0008g0349 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-43-5292_-43-5282d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | |||||
| chr16:15659425
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0332a0001c0001t0002g0333 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-43-5293_-43-5282d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | |||||
| chr16:15659598
|
G | A | 30 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(27): Show | 30 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-43-5138G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659598 | ||||||
| chr16:15659609
|
A | C | 1 | a0001c0001t0018g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-43-5127A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659609 | ||||||
| chr16:15659693
|
T | C | 4 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(1): Show | 4 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-5043T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659693 | ||||||
| chr16:15659729
|
G | A | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-5007G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659729 | ||||||
| chr16:15659748
|
CT | C | 34 | a0001c0001t0001g0057a0001c0001t0002g0012a0001c0001t0003g0127others(31): Show | 34 | HG01109.hp2 HG01168.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.-43-4970delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659748 | |||||
| chr16:15659926
|
T | G | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-43-4810T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659926 | ||||||
| chr16:15659993
|
C | G | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-43-4743C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659993 | ||||||
| chr16:15659998
|
C | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-4738C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659998 | ||||||
| chr16:15660136
|
C | G | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-4600C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660136 | ||||||
| chr16:15660262
|
G | C | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-4474G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660262 | ||||||
| chr16:15660342
|
C | G | 12 | a0001c0001t0006g0018a0001c0001t0011g0003a0001c0001t0011g0004others(9): Show | 12 | HG01496.hp2 HG02040.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-4394C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660342 | ||||||
| chr16:15660544
|
G | A | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-4192G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660544 | ||||||
| chr16:15660570
|
T | C | 1 | a0001c0001t0004g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-43-4166T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660570 | ||||||
| chr16:15660580
|
C | T | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-4156C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660580 | ||||||
| chr16:15660611
|
G | T | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-43-4125G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660611 | ||||||
| chr16:15660696
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43-4040C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660696 | ||||||
| chr16:15660716
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4020C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660716 | ||||||
| chr16:15660788
|
G | C | 10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-3948G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660788 | ||||||
| chr16:15661156
|
G | GT | 23 | a0001c0001t0002g0270a0001c0001t0003g0120a0001c0001t0003g0144others(20): Show | 23 | HG01106.hp2 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-3564dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661156 | |||||
| chr16:15661156
|
G | T | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-43-3580G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661156 | ||||||
| chr16:15661156
|
GT | G | 141 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-43-3564delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661156 | |||||
| chr16:15661188
|
A | G | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-43-3548A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661188 | ||||||
| chr16:15661296
|
C | T | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-3440C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661296 | ||||||
| chr16:15661360
|
GA | G | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-43-3374delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661360 | |||||
| chr16:15661399
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-43-3337C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661399 | ||||||
| chr16:15661448
|
G | A | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-43-3288G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661448 | ||||||
| chr16:15661557
|
C | T | 6 | a0001c0001t0004g0181a0001c0001t0004g0182a0001c0001t0004g0183others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-3179C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661557 | ||||||
| chr16:15661800
|
A | G | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-2936A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661800 | ||||||
| chr16:15661888
|
C | G | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-2848C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661888 | ||||||
| chr16:15661995
|
G | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-43-2741G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661995 | ||||||
| chr16:15662094
|
A | G | 1 | a0001c0001t0002g0338 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43-2642A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662094 | ||||||
| chr16:15662095
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-43-2641G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662095 | ||||||
| chr16:15662280
|
C | CT | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0086others(7): Show | 10 | HG00597.hp1 HG01123.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-2436dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15662280 | |||||
| chr16:15662280
|
CT | C | 6 | a0001c0001t0001g0058a0001c0001t0003g0111a0001c0001t0007g0324others(3): Show | 6 | HG00140.hp2 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-2436delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15662280 | |||||
| chr16:15662356
|
C | T | 19 | a0001c0001t0006g0018a0001c0001t0008g0348a0001c0001t0008g0349others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-2380C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662356 | ||||||
| chr16:15662630
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0039 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-43-2106G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662630 | ||||||
| chr16:15662678
|
G | T | 1 | a0001c0001t0001g0341 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-43-2058G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662678 | ||||||
| chr16:15662790
|
G | T | 24 | a0001c0001t0006g0018a0001c0001t0008g0348a0001c0001t0008g0349others(21): Show | 24 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1946G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662790 | ||||||
| chr16:15662807
|
A | G | 24 | a0001c0001t0006g0018a0001c0001t0008g0348a0001c0001t0008g0349others(21): Show | 24 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1929A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662807 | ||||||
| chr16:15662817
|
G | A | 2 | a0001c0001t0030g0311a0001c0001t0031g0017 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-1919G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662817 | ||||||
| chr16:15662858
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1878C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662858 | ||||||
| chr16:15662919
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-43-1817C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662919 | ||||||
| chr16:15663045
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-43-1691G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663045 | ||||||
| chr16:15663052
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-43-1684A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663052 | ||||||
| chr16:15663101
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-43-1635C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663101 | ||||||
| chr16:15663216
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-43-1520C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663216 | ||||||
| chr16:15663241
|
CT | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0194a0001c0001t0001g0289others(13): Show | 16 | HG01168.hp1 HG02040.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-1479delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15663241 | |||||
| chr16:15663266
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-1470G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663266 | ||||||
| chr16:15663396
|
C | G | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-1340C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663396 | ||||||
| chr16:15663414
|
A | AT | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-43-1313dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15663414 | |||||
| chr16:15663478
|
G | A | 205 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(202): Show | 205 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-43-1258G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663478 | ||||||
| chr16:15663605
|
G | A | 2 | a0001c0002t0001g0216a0001c0002t0001g0329 | 2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-43-1131G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663605 | ||||||
| chr16:15663750
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-986A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663750 | ||||||
| chr16:15663806
|
C | CTGGG | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-930_-43-929ins others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663806 | ||||||
| chr16:15663807
|
C | T | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-929C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663807 | ||||||
| chr16:15663808
|
T | G | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-928T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663808 | ||||||
| chr16:15663811
|
A | T | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-925A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663811 | ||||||
| chr16:15663812
|
A | C | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-924A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663812 | ||||||
| chr16:15663813
|
T | A | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-923T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663813 | ||||||
| chr16:15663814
|
A | C | 6 | a0001c0001t0002g0107a0001c0001t0002g0283a0001c0001t0006g0267others(3): Show | 6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-922A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663814 | ||||||
| chr16:15664120
|
C | CT | 5 | a0001c0001t0010g0101a0001c0001t0010g0102a0001c0001t0010g0103others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-615dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15664120 | |||||
| chr16:15664127
|
A | T | 5 | a0001c0001t0010g0101a0001c0001t0010g0102a0001c0001t0010g0103others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-609A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664127 | ||||||
| chr16:15664136
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-43-600A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664136 | ||||||
| chr16:15664225
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-511A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664225 | ||||||
| chr16:15664456
|
A | G | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-280A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664456 | ||||||
| chr16:15664472
|
T | C | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43-264T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664472 | ||||||
| chr16:15664635
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43-101G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664635 | ||||||
| chr16:15664887
|
CT | C | 28 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0287others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.83+42delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 15664887 | |||||
| chr16:15664986
|
C | T | 1 | a0001c0001t0003g0123 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.83+125C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15664986 | ||||||
| chr16:15665049
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.83+188T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665049 | ||||||
| chr16:15665220
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+359A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665220 | ||||||
| chr16:15665262
|
A | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.83+401A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665262 | ||||||
| chr16:15665352
|
C | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+491C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665352 | ||||||
| chr16:15665718
|
T | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.83+857T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665718 | ||||||
| chr16:15665867
|
T | C | 268 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.83+1006T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665867 | ||||||
| chr16:15665906
|
A | G | 261 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(258): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.83+1045A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665906 | ||||||
| chr16:15665944
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.83+1083C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665944 | ||||||
| chr16:15665956
|
A | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0142 | 2 | HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.83+1095A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665956 | ||||||
| chr16:15666035
|
C | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 8 | HG00597.hp1 HG02083.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+1174C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666035 | ||||||
| chr16:15666051
|
C | T | 2 | a0001c0001t0030g0311a0001c0001t0031g0017 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.83+1190C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666051 | ||||||
| chr16:15666158
|
T | C | 31 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(28): Show | 31 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-1128T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666158 | ||||||
| chr16:15666230
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-1056C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666230 | ||||||
| chr16:15666553
|
G | A | 1 | a0001c0001t0009g0358 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.84-733G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666553 | ||||||
| chr16:15666741
|
C | T | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-545C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666741 | ||||||
| chr16:15666851
|
T | A | 1 | a0001c0001t0016g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.84-435T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666851 | ||||||
| chr16:15666882
|
A | G | 1 | a0001c0001t0002g0266 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.84-404A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666882 | ||||||
| chr16:15666915
|
G | T | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-371G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666915 | ||||||
| chr16:15666938
|
A | G | 1 | a0001c0001t0002g0265 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.84-348A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666938 | ||||||
| chr16:15666945
|
T | A | 2 | a0001c0001t0004g0181a0001c0001t0004g0182 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.84-341T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666945 | ||||||
| chr16:15666983
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84-303C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666983 | ||||||
| chr16:15667141
|
G | A | 2 | a0001c0001t0006g0018a0001c0001t0032g0019 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.84-145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15667141 | ||||||
| chr16:15667520
|
C | A | 10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.237+81C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667520 | ||||||
| chr16:15667542
|
C | G | 19 | a0001c0001t0006g0018a0001c0001t0008g0348a0001c0001t0008g0349others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+103C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667542 | ||||||
| chr16:15667574
|
T | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.237+135T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667574 | ||||||
| chr16:15667576
|
C | G | 270 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.237+137C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667576 | ||||||
| chr16:15667627
|
G | GT | 80 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0034others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.237+192dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | |||||
| chr16:15667627
|
G | GTT | 72 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.237+191_237+192dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | |||||
| chr16:15667627
|
G | GTTT | 7 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0076others(4): Show | 7 | HG01433.hp2 HG02135.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+190_237+192dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | |||||
| chr16:15667632
|
G | T | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.237+193G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667632 | ||||||
| chr16:15667633
|
T | TTG | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG00735.hp2 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+195_237+196ins others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667633 | |||||
| chr16:15667634
|
T | G | 31 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.237+195T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667634 | ||||||
| chr16:15667638
|
T | G | 3 | a0001c0001t0003g0149a0001c0001t0003g0310a0001c0001t0003g0365 | 3 | NA18960.hp1 NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237+199T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667638 | ||||||
| chr16:15667788
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.237+349C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667788 | ||||||
| chr16:15667865
|
C | T | 2 | a0001c0001t0006g0018a0001c0001t0032g0019 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+426C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667865 | ||||||
| chr16:15667926
|
T | A | 21 | a0001c0001t0002g0224a0001c0001t0002g0228a0001c0001t0002g0229others(18): Show | 21 | HG03834.hp2 NA18940.hp1 NA18946.hp1 others(18): Show |
intron_variant | MODIFIER | c.237+487T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667926 | ||||||
| chr16:15667968
|
C | CT | 12 | a0001c0001t0002g0265a0001c0001t0002g0284a0001c0001t0003g0140others(9): Show | 12 | HG02738.hp1 NA18940.hp1 NA18973.hp2 others(9): Show |
intron_variant | MODIFIER | c.237+543dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667968 | |||||
| chr16:15667968
|
CT | C | 17 | a0001c0001t0001g0050a0001c0001t0002g0228a0001c0001t0002g0270others(14): Show | 17 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.237+543delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667968 | |||||
| chr16:15668190
|
T | C | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.237+751T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668190 | ||||||
| chr16:15668261
|
G | A | 1 | a0001c0001t0020g0093 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.237+822G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668261 | ||||||
| chr16:15668269
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.237+830A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668269 | ||||||
| chr16:15668350
|
C | G | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+911C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668350 | ||||||
| chr16:15668418
|
C | T | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.237+979C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668418 | ||||||
| chr16:15668454
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.237+1015A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668454 | ||||||
| chr16:15668497
|
G | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+1058G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668497 | ||||||
| chr16:15668602
|
A | G | 3 | a0001c0001t0002g0264a0001c0001t0002g0363a0001c0001t0002g0364 | 3 | HG02622.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.237+1163A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668602 | ||||||
| chr16:15668607
|
A | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+1168A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668607 | ||||||
| chr16:15668821
|
G | C | 2 | a0001c0001t0006g0018a0001c0001t0032g0019 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+1382G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668821 | ||||||
| chr16:15668852
|
T | A | 1 | a0001c0001t0002g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.237+1413T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668852 | ||||||
| chr16:15668868
|
G | A | 1 | a0001c0001t0019g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.237+1429G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668868 | ||||||
| chr16:15668961
|
G | A | 1 | a0001c0001t0002g0338 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.237+1522G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668961 | ||||||
| chr16:15668969
|
G | A | 1 | a0001c0001t0005g0163 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.237+1530G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668969 | ||||||
| chr16:15668980
|
A | C | 2 | a0001c0001t0006g0018a0001c0001t0032g0019 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+1541A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668980 | ||||||
| chr16:15669044
|
C | T | 75 | a0001c0001t0001g0309a0001c0001t0001g0347a0001c0001t0002g0012others(72): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.237+1605C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669044 | ||||||
| chr16:15669142
|
C | T | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.237+1703C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669142 | ||||||
| chr16:15669143
|
G | A | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1704G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669143 | ||||||
| chr16:15669159
|
CA | C | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1723delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15669159 | |||||
| chr16:15669196
|
A | G | 133 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(130): Show | 133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.237+1757A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669196 | ||||||
| chr16:15669255
|
A | T | 91 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.237+1816A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669255 | ||||||
| chr16:15669306
|
G | A | 133 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(130): Show | 133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.237+1867G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669306 | ||||||
| chr16:15669360
|
A | AT | 23 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0055others(20): Show | 23 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.237+1941dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15669360 | |||||
| chr16:15669679
|
A | C | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.237+2240A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669679 | ||||||
| chr16:15669725
|
G | C | 268 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.237+2286G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669725 | ||||||
| chr16:15669781
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237+2342C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669781 | ||||||
| chr16:15670184
|
A | G | 1 | a0001c0001t0038g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237+2745A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670184 | ||||||
| chr16:15670228
|
T | G | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.237+2789T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670228 | ||||||
| chr16:15670386
|
G | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+2947G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670386 | ||||||
| chr16:15670554
|
G | A | 7 | a0001c0001t0002g0230a0001c0001t0002g0241a0001c0001t0002g0242others(4): Show | 7 | HG00423.hp1 NA18960.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+3115G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670554 | ||||||
| chr16:15670657
|
C | CA | 19 | a0001c0001t0002g0284a0001c0001t0008g0348a0001c0001t0008g0349others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+3233dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670657 | |||||
| chr16:15670657
|
CA | C | 115 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(112): Show | 115 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.237+3233delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670657 | |||||
| chr16:15670677
|
GAAAA | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0288a0001c0001t0001g0289others(17): Show | 20 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.237+3240_237+3243d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670677 | |||||
| chr16:15670940
|
T | C | 5 | a0001c0002t0001g0160a0001c0002t0001g0191a0001c0002t0001g0192others(2): Show | 5 | HG00738.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+3501T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670940 | ||||||
| chr16:15671176
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0278 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.237+3737C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671176 | ||||||
| chr16:15671317
|
A | G | 5 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+3878A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671317 | ||||||
| chr16:15671354
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0061others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.237+3915T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671354 | ||||||
| chr16:15671513
|
A | G | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.237+4074A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671513 | ||||||
| chr16:15671546
|
T | C | 107 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(104): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.237+4107T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671546 | ||||||
| chr16:15671838
|
C | T | 21 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(18): Show | 21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.237+4399C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671838 | ||||||
| chr16:15671889
|
A | C | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237+4450A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671889 | ||||||
| chr16:15672116
|
T | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+4677T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672116 | ||||||
| chr16:15672123
|
G | C | 130 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(127): Show | 130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.237+4684G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672123 | ||||||
| chr16:15672200
|
C | T | 6 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(3): Show | 6 | HG01433.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+4761C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672200 | ||||||
| chr16:15672254
|
G | A | 1 | a0001c0001t0003g0066 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.237+4815G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672254 | ||||||
| chr16:15672262
|
G | A | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+4823G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672262 | ||||||
| chr16:15672533
|
G | T | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.237+5094G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672533 | ||||||
| chr16:15672607
|
G | A | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237+5168G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672607 | ||||||
| chr16:15672721
|
G | A | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.238-5080G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672721 | ||||||
| chr16:15672746
|
C | G | 2 | a0001c0001t0003g0111a0001c0001t0003g0118 | 2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.238-5055C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672746 | ||||||
| chr16:15672798
|
T | C | 1 | a0001c0001t0003g0022 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.238-5003T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672798 | ||||||
| chr16:15672851
|
C | T | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-4950C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672851 | ||||||
| chr16:15672969
|
G | A | 25 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(22): Show | 25 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.238-4832G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672969 | ||||||
| chr16:15673152
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0034 | 2 | HG00438.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.238-4649C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673152 | ||||||
| chr16:15673329
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.238-4472G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673329 | ||||||
| chr16:15673392
|
C | T | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-4409C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673392 | ||||||
| chr16:15673451
|
C | T | 2 | a0001c0001t0012g0312a0001c0001t0012g0313 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.238-4350C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673451 | ||||||
| chr16:15673488
|
C | T | 4 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(1): Show | 4 | HG02040.hp1 HG02818.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-4313C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673488 | ||||||
| chr16:15673547
|
AT | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0067a0001c0001t0001g0211others(5): Show | 8 | HG01167.hp1 HG02273.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-4238delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15673547 | |||||
| chr16:15673568
|
G | A | 2 | a0001c0001t0014g0344a0001c0001t0014g0346 | 2 | NA18952.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.238-4233G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673568 | ||||||
| chr16:15673680
|
A | G | 8 | a0001c0001t0005g0175a0001c0001t0005g0176a0001c0001t0005g0177others(5): Show | 8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-4121A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673680 | ||||||
| chr16:15673995
|
A | G | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-3806A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673995 | ||||||
| chr16:15674002
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.238-3799G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674002 | ||||||
| chr16:15674013
|
T | G | 1 | a0001c0001t0002g0272 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.238-3788T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674013 | ||||||
| chr16:15674114
|
G | A | 1 | a0001c0001t0038g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.238-3687G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674114 | ||||||
| chr16:15674140
|
G | A | 232 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(229): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.238-3661G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674140 | ||||||
| chr16:15674192
|
C | T | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.238-3609C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674192 | ||||||
| chr16:15674324
|
AC | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3475delC | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15674324 | |||||
| chr16:15674373
|
G | A | 244 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(241): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.238-3428G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674373 | ||||||
| chr16:15674392
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0061others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.238-3409G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674392 | ||||||
| chr16:15674449
|
A | G | 1 | a0001c0001t0009g0357 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.238-3352A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674449 | ||||||
| chr16:15674533
|
G | A | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-3268G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674533 | ||||||
| chr16:15674564
|
A | T | 5 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0128others(2): Show | 6 | HG00642.hp1 HG02135.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-3237A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674564 | ||||||
| chr16:15674587
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238-3214C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674587 | ||||||
| chr16:15674616
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.238-3185G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674616 | ||||||
| chr16:15674658
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3143C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674658 | ||||||
| chr16:15674728
|
A | G | 1 | a0001c0001t0018g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.238-3073A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674728 | ||||||
| chr16:15674766
|
C | T | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.238-3035C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674766 | ||||||
| chr16:15674771
|
A | G | 1 | a0001c0001t0004g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238-3030A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674771 | ||||||
| chr16:15674780
|
C | T | 1 | a0001c0001t0002g0272 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.238-3021C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674780 | ||||||
| chr16:15674845
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238-2956C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674845 | ||||||
| chr16:15674853
|
G | A | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-2948G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674853 | ||||||
| chr16:15674855
|
C | T | 1 | a0001c0001t0003g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.238-2946C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674855 | ||||||
| chr16:15675077
|
T | C | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-2724T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675077 | ||||||
| chr16:15675284
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.238-2517C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675284 | ||||||
| chr16:15675303
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.238-2498A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675303 | ||||||
| chr16:15675352
|
C | T | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-2449C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675352 | ||||||
| chr16:15675424
|
G | GT | 15 | a0001c0001t0002g0240a0001c0001t0002g0243a0001c0001t0002g0261others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.238-2362dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15675424 | |||||
| chr16:15675424
|
GT | G | 206 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(203): Show | 207 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.238-2362delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15675424 | |||||
| chr16:15675444
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.238-2357G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675444 | ||||||
| chr16:15675495
|
G | A | 2 | a0001c0001t0005g0164a0001c0001t0005g0165 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.238-2306G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675495 | ||||||
| chr16:15675508
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0091 | 3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.238-2293C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675508 | ||||||
| chr16:15675510
|
C | T | 218 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(215): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.238-2291C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675510 | ||||||
| chr16:15675536
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.238-2265A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675536 | ||||||
| chr16:15675587
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.238-2214C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675587 | ||||||
| chr16:15675632
|
T | G | 1 | a0001c0001t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238-2169T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675632 | ||||||
| chr16:15675687
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238-2114A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675687 | ||||||
| chr16:15675818
|
T | A | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-1983T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675818 | ||||||
| chr16:15676024
|
T | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1777T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676024 | ||||||
| chr16:15676035
|
G | A | 20 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(17): Show | 20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.238-1766G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676035 | ||||||
| chr16:15676086
|
CAT | C | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-1713_238-1712d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676086 | |||||
| chr16:15676089
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.238-1712A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676089 | ||||||
| chr16:15676143
|
TTCCTCTC | T | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-1648_238-1642d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676143 | |||||
| chr16:15676225
|
G | GT | 252 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(249): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.238-1559dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676225 | |||||
| chr16:15676225
|
G | GTT | 9 | a0001c0001t0001g0044a0001c0001t0001g0091a0001c0001t0001g0330others(6): Show | 9 | HG00642.hp1 HG01515.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-1560_238-1559d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676225 | |||||
| chr16:15676226
|
T | G | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-1575T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676226 | ||||||
| chr16:15676295
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.238-1506C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676295 | ||||||
| chr16:15676336
|
A | C | 2 | a0001c0001t0002g0335a0001c0001t0002g0340 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.238-1465A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676336 | ||||||
| chr16:15676559
|
C | G | 1 | a0001c0001t0002g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.238-1242C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676559 | ||||||
| chr16:15676748
|
C | G | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.238-1053C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676748 | ||||||
| chr16:15676786
|
C | T | 260 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(257): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.238-1015C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676786 | ||||||
| chr16:15676940
|
G | A | 2 | a0001c0001t0030g0311a0001c0001t0031g0017 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.238-861G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676940 | ||||||
| chr16:15676957
|
G | T | 12 | a0001c0001t0002g0224a0001c0001t0002g0229a0001c0001t0002g0232others(9): Show | 12 | HG03834.hp2 NA18950.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-844G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676957 | ||||||
| chr16:15676998
|
G | A | 1 | a0001c0001t0016g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.238-803G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676998 | ||||||
| chr16:15677001
|
T | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-800T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677001 | ||||||
| chr16:15677107
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238-694G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677107 | ||||||
| chr16:15677246
|
G | A | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0144 | 3 | HG01106.hp2 HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.238-555G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677246 | ||||||
| chr16:15677288
|
A | G | 1 | a0001c0001t0008g0362 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238-513A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677288 | ||||||
| chr16:15677349
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.238-452C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677349 | ||||||
| chr16:15677401
|
C | T | 3 | a0001c0001t0014g0344a0001c0001t0014g0345a0001c0001t0014g0346 | 3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.238-400C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677401 | ||||||
| chr16:15677422
|
C | T | 1 | a0001c0001t0035g0209 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238-379C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677422 | ||||||
| chr16:15677538
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.238-263A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677538 | ||||||
| chr16:15677590
|
G | GA | 8 | a0001c0001t0001g0082a0001c0001t0001g0293a0001c0001t0002g0275others(5): Show | 8 | HG02135.hp2 HG02280.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-198dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15677590 | |||||
| chr16:15677741
|
C | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.238-60C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677741 | ||||||
| chr16:15677744
|
T | C | 268 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.238-57T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677744 | ||||||
| chr16:15677762
|
G | A | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-39G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677762 | ||||||
| chr16:15677990
|
C | G | 64 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0008others(61): Show | 65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.386+41C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15677990 | ||||||
| chr16:15678074
|
C | A | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+125C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678074 | ||||||
| chr16:15678094
|
G | A | 64 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0008others(61): Show | 65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.386+145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678094 | ||||||
| chr16:15678101
|
A | T | 1 | a0001c0001t0006g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.386+152A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678101 | ||||||
| chr16:15678290
|
T | C | 1 | a0001c0001t0002g0315 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.386+341T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678290 | ||||||
| chr16:15678422
|
T | C | 1 | a0001c0001t0009g0357 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.386+473T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678422 | ||||||
| chr16:15678467
|
C | T | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.386+518C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678467 | ||||||
| chr16:15678555
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.386+606G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678555 | ||||||
| chr16:15678595
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0307 | 2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.386+646G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678595 | ||||||
| chr16:15678632
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+683C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678632 | ||||||
| chr16:15678852
|
G | A | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386+903G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678852 | ||||||
| chr16:15678906
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.386+957C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678906 | ||||||
| chr16:15678985
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.386+1036A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678985 | ||||||
| chr16:15679008
|
C | T | 2 | a0001c0001t0007g0323a0001c0001t0007g0324 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.386+1059C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679008 | ||||||
| chr16:15679009
|
G | A | 65 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0008others(62): Show | 66 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.386+1060G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679009 | ||||||
| chr16:15679055
|
T | C | 365 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(362): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.386+1106T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679055 | ||||||
| chr16:15679348
|
C | T | 2 | a0001c0001t0006g0121a0001c0001t0006g0286 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.386+1399C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679348 | ||||||
| chr16:15679354
|
C | G | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.386+1405C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679354 | ||||||
| chr16:15679529
|
T | C | 1 | a0001c0001t0004g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.386+1580T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679529 | ||||||
| chr16:15679628
|
G | A | 21 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(18): Show | 21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+1679G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679628 | ||||||
| chr16:15679756
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386+1807T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679756 | ||||||
| chr16:15679775
|
GTTT | G | 4 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+1830_386+1832d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15679775 | |||||
| chr16:15679782
|
G | GTT | 21 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.386+1837_386+1838d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15679782 | |||||
| chr16:15679902
|
C | T | 5 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01496.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+1953C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679902 | ||||||
| chr16:15679903
|
G | A | 1 | a0001c0001t0002g0339 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.386+1954G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679903 | ||||||
| chr16:15680030
|
C | T | 4 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014others(1): Show | 4 | HG02040.hp1 HG02818.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+2081C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680030 | ||||||
| chr16:15680294
|
G | A | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2345G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680294 | ||||||
| chr16:15680456
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.386+2507C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680456 | ||||||
| chr16:15680564
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.386+2615C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680564 | ||||||
| chr16:15680568
|
C | T | 30 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(27): Show | 30 | HG01261.hp2 HG01496.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.386+2619C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680568 | ||||||
| chr16:15680820
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.386+2871G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680820 | ||||||
| chr16:15680922
|
A | G | 42 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(39): Show | 42 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.386+2973A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680922 | ||||||
| chr16:15680925
|
G | C | 107 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(104): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.386+2976G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680925 | ||||||
| chr16:15681174
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.386+3225A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681174 | ||||||
| chr16:15681195
|
T | G | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+3246T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681195 | ||||||
| chr16:15681224
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18980.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.386+3275C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681224 | ||||||
| chr16:15681253
|
C | CT | 35 | a0001c0001t0001g0257a0001c0001t0002g0219a0001c0001t0002g0223others(32): Show | 35 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.386+3334dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTT | 11 | a0001c0001t0004g0162a0001c0001t0004g0166a0001c0001t0004g0168others(8): Show | 11 | HG01261.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.386+3333_386+3334d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTT | 7 | a0001c0001t0004g0105a0001c0001t0004g0167a0001c0001t0004g0181others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+3332_386+3334d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTT | 15 | a0001c0001t0001g0347a0001c0001t0004g0171a0001c0001t0004g0186others(12): Show | 15 | HG00140.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.386+3331_386+3334d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTT | 25 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG00609.hp2 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.386+3330_386+3334d others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTT | 49 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(46): Show | 50 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.386+3329_386+3334d others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT | 44 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0033others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.386+3328_386+3334d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(1): Show |
40 | a0001c0001t0001g0032a0001c0001t0001g0089a0001c0001t0001g0090others(37): Show | 40 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.386+3327_386+3334d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0020a0001c0001t0001g0068a0001c0001t0001g0072others(23): Show | 26 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+3326_386+3334d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(3): Show |
26 | a0001c0001t0001g0038a0001c0001t0001g0069a0001c0001t0001g0097others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.386+3325_386+3334d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0203a0001c0001t0001g0212a0001c0001t0001g0289others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+3324_386+3334d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+3323_386+3334d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0010g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.386+3322_386+3334d others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681253
|
CT | C | 9 | a0001c0001t0002g0098a0001c0001t0002g0226a0001c0001t0002g0243others(6): Show | 9 | HG01891.hp1 HG02040.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+3334delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | |||||
| chr16:15681302
|
A | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+3353A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681302 | ||||||
| chr16:15681322
|
A | G | 31 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(28): Show | 31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.386+3373A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681322 | ||||||
| chr16:15681436
|
T | C | 1 | a0001c0001t0004g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386+3487T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681436 | ||||||
| chr16:15681611
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+3662C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681611 | ||||||
| chr16:15681735
|
C | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386+3786C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681735 | ||||||
| chr16:15681781
|
C | T | 2 | a0001c0001t0019g0042a0001c0001t0019g0043 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.386+3832C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681781 | ||||||
| chr16:15682132
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.386+4183G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682132 | ||||||
| chr16:15682133
|
G | A | 21 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(18): Show | 21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+4184G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682133 | ||||||
| chr16:15682230
|
C | T | 35 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(32): Show | 35 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.386+4281C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682230 | ||||||
| chr16:15682507
|
C | T | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.386+4558C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682507 | ||||||
| chr16:15682655
|
G | A | 1 | a0001c0001t0029g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.386+4706G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682655 | ||||||
| chr16:15682658
|
A | G | 21 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(18): Show | 21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+4709A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682658 | ||||||
| chr16:15682879
|
T | C | 8 | a0001c0001t0005g0175a0001c0001t0005g0176a0001c0001t0005g0177others(5): Show | 8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-4496T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682879 | ||||||
| chr16:15683046
|
A | G | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.387-4329A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683046 | ||||||
| chr16:15683053
|
C | T | 210 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(207): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.387-4322C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683053 | ||||||
| chr16:15683281
|
T | C | 1 | a0001c0001t0033g0296 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.387-4094T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683281 | ||||||
| chr16:15683343
|
G | GT | 7 | a0001c0001t0001g0013a0001c0001t0002g0255a0001c0001t0002g0261others(4): Show | 7 | HG00558.hp1 HG00597.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-4024dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15683343 | |||||
| chr16:15683400
|
T | C | 1 | a0001c0001t0015g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.387-3975T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683400 | ||||||
| chr16:15683408
|
A | G | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-3967A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683408 | ||||||
| chr16:15683635
|
G | A | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387-3740G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683635 | ||||||
| chr16:15683888
|
A | G | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387-3487A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683888 | ||||||
| chr16:15683900
|
G | C | 2 | a0001c0001t0005g0164a0001c0001t0005g0165 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.387-3475G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683900 | ||||||
| chr16:15683919
|
C | T | 210 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(207): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.387-3456C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683919 | ||||||
| chr16:15684023
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.387-3352G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684023 | ||||||
| chr16:15684129
|
A | T | 1 | a0001c0001t0003g0120 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.387-3246A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684129 | ||||||
| chr16:15684463
|
C | T | 1 | a0001c0001t0036g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.387-2912C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684463 | ||||||
| chr16:15684529
|
G | T | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.387-2846G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684529 | ||||||
| chr16:15684556
|
G | C | 1 | a0001c0001t0002g0337 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.387-2819G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684556 | ||||||
| chr16:15684568
|
T | TA | 35 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0074others(32): Show | 35 | HG00408.hp2 HG00639.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.387-2789dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15684568 | |||||
| chr16:15684568
|
TA | T | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0002g0107others(7): Show | 10 | HG01256.hp2 HG02897.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-2789delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15684568 | |||||
| chr16:15685232
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.387-2143C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685232 | ||||||
| chr16:15685350
|
G | A | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.387-2025G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685350 | ||||||
| chr16:15685379
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387-1996G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685379 | ||||||
| chr16:15685411
|
C | T | 9 | a0001c0001t0002g0275a0001c0001t0005g0175a0001c0001t0005g0176others(6): Show | 9 | NA18973.hp2 NA18991.hp2 NA18995.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-1964C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685411 | ||||||
| chr16:15685412
|
G | A | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387-1963G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685412 | ||||||
| chr16:15685469
|
T | G | 1 | a0001c0001t0001g0330 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.387-1906T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685469 | ||||||
| chr16:15685482
|
C | T | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.387-1893C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685482 | ||||||
| chr16:15685582
|
T | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0039 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.387-1793T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685582 | ||||||
| chr16:15685634
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1741C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685634 | ||||||
| chr16:15685712
|
T | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1663T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685712 | ||||||
| chr16:15685953
|
A | AT | 10 | a0001c0001t0001g0027a0001c0001t0002g0265a0001c0001t0003g0139others(7): Show | 10 | HG00621.hp2 HG01496.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-1406dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15685953 | |||||
| chr16:15686032
|
A | G | 1 | a0001c0001t0003g0066 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.387-1343A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686032 | ||||||
| chr16:15686054
|
C | T | 8 | a0001c0001t0002g0228a0001c0001t0002g0231a0001c0001t0002g0234others(5): Show | 8 | NA18940.hp1 NA18946.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-1321C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686054 | ||||||
| chr16:15686241
|
C | T | 1 | a0001c0001t0035g0209 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.387-1134C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686241 | ||||||
| chr16:15686366
|
T | TTATAACA others(6062): Show |
1 | a0001c0001t0001g0342 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.387-990_387-989ins others(6069): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15686366 | |||||
| chr16:15686366
|
T | TTATAACA others(6064): Show |
1 | a0001c0001t0001g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.387-990_387-989ins others(6071): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15686366 | |||||
| chr16:15686459
|
C | A | 4 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-916C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686459 | ||||||
| chr16:15686510
|
C | T | 56 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(53): Show | 56 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.387-865C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686510 | ||||||
| chr16:15686553
|
C | G | 1 | a0001c0001t0002g0237 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.387-822C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686553 | ||||||
| chr16:15686644
|
C | G | 21 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(18): Show | 21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.387-731C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686644 | ||||||
| chr16:15686841
|
A | G | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-534A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686841 | ||||||
| chr16:15686875
|
G | C | 1 | a0001c0001t0003g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.387-500G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686875 | ||||||
| chr16:15687091
|
T | G | 1 | a0001c0001t0009g0355 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.387-284T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687091 | ||||||
| chr16:15687197
|
A | G | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.387-178A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687197 | ||||||
| chr16:15687231
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.387-144C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687231 | ||||||
| chr16:15687235
|
G | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0193a0001c0001t0001g0199others(5): Show | 8 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-140G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687235 | ||||||
| chr16:15687335
|
G | C | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-40G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687335 | ||||||
| chr16:15687612
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.523+101A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15687612 | ||||||
| chr16:15687647
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.523+136G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15687647 | ||||||
| chr16:15688088
|
A | G | 5 | a0001c0001t0002g0230a0001c0001t0002g0241a0001c0001t0002g0244others(2): Show | 5 | HG00423.hp1 NA18975.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+577A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688088 | ||||||
| chr16:15688540
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.523+1029C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688540 | ||||||
| chr16:15688633
|
C | CA | 44 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0071others(41): Show | 44 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.523+1142dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688633 | |||||
| chr16:15688633
|
CA | C | 17 | a0001c0001t0001g0038a0001c0001t0001g0201a0001c0001t0002g0040others(14): Show | 17 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.523+1142delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688633 | |||||
| chr16:15688689
|
C | CT | 35 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0089others(32): Show | 35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.523+1205dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTT | 6 | a0001c0001t0001g0030a0001c0001t0002g0252a0001c0001t0002g0253others(3): Show | 6 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+1204_523+1205d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTT | 42 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(39): Show | 43 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.523+1203_523+1205d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTT | 38 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0347others(35): Show | 38 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.523+1202_523+1205d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTT | 17 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0288others(14): Show | 17 | HG01109.hp2 HG01516.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.523+1201_523+1205d others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTT | 25 | a0001c0001t0001g0059a0001c0001t0001g0194a0001c0001t0001g0195others(22): Show | 25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+1200_523+1205d others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT | 35 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0034others(32): Show | 35 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.523+1199_523+1205d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT others(1): Show |
29 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0044others(26): Show | 29 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.523+1198_523+1205d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT others(2): Show |
24 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0054others(21): Show | 24 | HG00609.hp2 HG00733.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.523+1197_523+1205d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0020a0001c0001t0001g0068a0001c0001t0001g0070others(8): Show | 11 | HG00642.hp2 HG01358.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.523+1196_523+1205d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0212 | 2 | HG00741.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.523+1195_523+1205d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.523+1194_523+1205d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
CT | C | 9 | a0001c0001t0001g0155a0001c0001t0002g0012a0001c0001t0002g0107others(6): Show | 9 | HG02040.hp1 HG02155.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.523+1205delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
CTTTTTTT others(2): Show |
C | 20 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(17): Show | 20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.523+1197_523+1205d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688689
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.523+1196_523+1205d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | |||||
| chr16:15688843
|
G | A | 1 | a0001c0001t0015g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.523+1332G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688843 | ||||||
| chr16:15688885
|
A | G | 212 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(209): Show | 213 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.523+1374A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688885 | ||||||
| chr16:15688920
|
ACTC | A | 28 | a0001c0001t0002g0107a0001c0001t0002g0224a0001c0001t0002g0228others(25): Show | 28 | HG00438.hp2 HG00621.hp2 HG03834.hp2 others(25): Show |
intron_variant | MODIFIER | c.523+1412_523+1414d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688920 | |||||
| chr16:15688935
|
C | T | 212 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(209): Show | 213 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.523+1424C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688935 | ||||||
| chr16:15689288
|
A | G | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523+1777A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689288 | ||||||
| chr16:15689446
|
T | A | 1 | a0001c0001t0026g0116 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.524-1698T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689446 | ||||||
| chr16:15689454
|
C | T | 3 | a0001c0001t0007g0325a0001c0001t0007g0326a0001c0001t0007g0328 | 3 | HG00140.hp2 HG01074.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.524-1690C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689454 | ||||||
| chr16:15689524
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.524-1620G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689524 | ||||||
| chr16:15689617
|
C | A | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.524-1527C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689617 | ||||||
| chr16:15689807
|
G | A | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.524-1337G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689807 | ||||||
| chr16:15689875
|
T | TG | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.524-1269_524-1268i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689875 | ||||||
| chr16:15689887
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.524-1257C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689887 | ||||||
| chr16:15689936
|
CT | C | 28 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(25): Show | 28 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.524-1207delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689936 | ||||||
| chr16:15689937
|
T | C | 4 | a0001c0001t0003g0111a0001c0001t0003g0123a0001c0001t0006g0018others(1): Show | 4 | HG03209.hp2 NA18522.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1207T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689937 | ||||||
| chr16:15689938
|
CA | C | 213 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(210): Show | 214 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.524-1185delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15689938 | |||||
| chr16:15689938
|
CAA | C | 12 | a0001c0001t0001g0156a0001c0001t0003g0111a0001c0001t0003g0137others(9): Show | 12 | HG01496.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.524-1186_524-1185d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15689938 | |||||
| chr16:15689939
|
A | C | 28 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(25): Show | 28 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.524-1205A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689939 | ||||||
| chr16:15690035
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1109C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690035 | ||||||
| chr16:15690068
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.524-1076T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690068 | ||||||
| chr16:15690133
|
C | G | 212 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(209): Show | 213 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.524-1011C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690133 | ||||||
| chr16:15690185
|
C | T | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-959C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690185 | ||||||
| chr16:15690190
|
G | C | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-954G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690190 | ||||||
| chr16:15690191
|
C | G | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-953C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690191 | ||||||
| chr16:15690200
|
A | G | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-944A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690200 | ||||||
| chr16:15690201
|
C | A | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-943C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690201 | ||||||
| chr16:15690202
|
G | C | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-942G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690202 | ||||||
| chr16:15690235
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.524-909G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690235 | ||||||
| chr16:15690336
|
C | CCTTTTTT others(8): Show |
3 | a0001c0001t0008g0360a0001c0001t0015g0214a0001c0001t0015g0215 | 3 | HG02970.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.524-807_524-793dup others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690336 | |||||
| chr16:15690337
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0008g0352 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.524-793_524-792ins others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690337 | |||||
| chr16:15690337
|
CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0002g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.524-791_524-764del others(28): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690337 | |||||
| chr16:15690338
|
T | TTTTTTTT others(7): Show |
3 | a0001c0001t0008g0351a0001c0001t0008g0353a0001c0001t0008g0362 | 3 | HG01109.hp2 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.524-793_524-792ins others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690338 | |||||
| chr16:15690339
|
T | TTTTTTTT others(6): Show |
5 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-793_524-792ins others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690339 | |||||
| chr16:15690340
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0007g0324 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.524-794_524-793ins others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690340 | |||||
| chr16:15690340
|
TTTTTTTT others(6): Show |
T | 14 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(11): Show | 14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-791_524-779del others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690340 | |||||
| chr16:15690341
|
T | TTTTTTTT others(3): Show |
2 | a0001c0001t0007g0323a0001c0001t0007g0326 | 2 | HG01074.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.524-794_524-793ins others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690341 | |||||
| chr16:15690342
|
TTTTTTTT others(4): Show |
T | 2 | a0001c0001t0004g0169a0001c0001t0004g0172 | 2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.524-791_524-781del others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690342 | |||||
| chr16:15690343
|
TTTTTTTT others(3): Show |
T | 18 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(15): Show | 18 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.524-791_524-782del others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690343 | |||||
| chr16:15690344
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.524-800T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690344 | ||||||
| chr16:15690353
|
C | CT | 82 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.524-763dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | |||||
| chr16:15690353
|
C | CTT | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(21): Show | 24 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.524-764_524-763dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | |||||
| chr16:15690353
|
C | CTTT | 6 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0100others(3): Show | 6 | HG00609.hp2 HG00735.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-765_524-763dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | |||||
| chr16:15690353
|
C | T | 33 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0156others(30): Show | 33 | HG00140.hp2 HG00597.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.524-791C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690353 | ||||||
| chr16:15690353
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0035g0209 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.524-774_524-763del others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | |||||
| chr16:15690353
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0005g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.524-775_524-763del others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | |||||
| chr16:15690354
|
T | C | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690354 | ||||||
| chr16:15690355
|
T | C | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.524-789T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690355 | ||||||
| chr16:15690356
|
T | C | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-788T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690356 | ||||||
| chr16:15690357
|
T | TC | 80 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(77): Show | 81 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.524-787_524-786ins others(1): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690357 | ||||||
| chr16:15690358
|
T | C | 1 | a0001c0001t0033g0296 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524-786T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690358 | ||||||
| chr16:15690359
|
T | C | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-785T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690359 | ||||||
| chr16:15690360
|
T | C | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-784T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690360 | ||||||
| chr16:15690362
|
T | C | 18 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(15): Show | 18 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.524-782T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690362 | ||||||
| chr16:15690363
|
T | C | 2 | a0001c0001t0004g0169a0001c0001t0004g0172 | 2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.524-781T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690363 | ||||||
| chr16:15690365
|
T | C | 14 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(11): Show | 14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-779T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690365 | ||||||
| chr16:15690433
|
C | CTG | 3 | a0001c0001t0002g0098a0001c0001t0002g0278a0001c0001t0002g0285 | 3 | HG03942.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.524-710_524-709dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690433 | |||||
| chr16:15690446
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.524-698T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690446 | ||||||
| chr16:15690505
|
G | A | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.524-639G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690505 | ||||||
| chr16:15690518
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.524-626C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690518 | ||||||
| chr16:15690526
|
T | A | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-618T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690526 | ||||||
| chr16:15690617
|
A | C | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-527A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690617 | ||||||
| chr16:15690672
|
A | G | 64 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(61): Show | 64 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.524-472A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690672 | ||||||
| chr16:15690829
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0039 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.524-315C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690829 | ||||||
| chr16:15691046
|
G | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0288a0001c0001t0001g0289others(18): Show | 21 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.524-98G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691046 | ||||||
| chr16:15691099
|
C | T | 3 | a0001c0001t0014g0344a0001c0001t0014g0345a0001c0001t0014g0346 | 3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.524-45C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691099 | ||||||
| chr16:15691100
|
G | A | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-44G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691100 | ||||||
| chr16:15691348
|
T | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.703+25T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691348 | ||||||
| chr16:15691504
|
T | G | 1 | a0001c0001t0006g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+181T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691504 | ||||||
| chr16:15691647
|
G | GT | 218 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(215): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.703+335dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | |||||
| chr16:15691647
|
G | GTT | 30 | a0001c0001t0001g0089a0001c0001t0003g0139a0001c0001t0004g0105others(27): Show | 30 | HG00423.hp2 HG01106.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.703+334_703+335dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | |||||
| chr16:15691647
|
G | GTTT | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+333_703+335dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | |||||
| chr16:15691787
|
C | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0061others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.703+464C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691787 | ||||||
| chr16:15691818
|
A | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.703+495A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691818 | ||||||
| chr16:15691889
|
C | A | 1 | a0001c0001t0008g0361 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+566C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691889 | ||||||
| chr16:15691892
|
A | T | 130 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(127): Show | 130 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.703+569A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691892 | ||||||
| chr16:15691922
|
C | T | 1 | a0001c0001t0008g0362 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+599C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691922 | ||||||
| chr16:15692031
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+708C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692031 | ||||||
| chr16:15692032
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.703+709G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692032 | ||||||
| chr16:15692047
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0039 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.703+724C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692047 | ||||||
| chr16:15692204
|
C | A | 1 | a0001c0001t0008g0362 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+881C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692204 | ||||||
| chr16:15692441
|
G | T | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703+1118G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692441 | ||||||
| chr16:15692517
|
C | G | 4 | a0001c0001t0002g0246a0001c0001t0002g0258a0001c0001t0002g0259others(1): Show | 4 | HG02818.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+1194C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692517 | ||||||
| chr16:15692554
|
G | A | 1 | a0001c0001t0023g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+1231G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692554 | ||||||
| chr16:15692611
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.703+1288T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692611 | ||||||
| chr16:15692862
|
G | C | 64 | a0001c0001t0001g0309a0001c0001t0003g0001a0001c0001t0003g0008others(61): Show | 65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.704-1303G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692862 | ||||||
| chr16:15692939
|
G | A | 12 | a0001c0001t0002g0220a0001c0001t0002g0270a0001c0001t0002g0314others(9): Show | 12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-1226G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692939 | ||||||
| chr16:15693003
|
C | CT | 18 | a0001c0001t0002g0230a0001c0001t0002g0241a0001c0001t0002g0242others(15): Show | 18 | HG00423.hp1 HG01074.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.704-1147dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15693003 | |||||
| chr16:15693127
|
G | A | 3 | a0001c0001t0002g0261a0001c0001t0002g0269a0001c0001t0002g0279 | 3 | HG02083.hp2 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.704-1038G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693127 | ||||||
| chr16:15693134
|
T | A | 1 | a0001c0001t0029g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704-1031T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693134 | ||||||
| chr16:15693180
|
T | G | 195 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(192): Show | 196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.704-985T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693180 | ||||||
| chr16:15693256
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.704-909C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693256 | ||||||
| chr16:15693302
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.704-863G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693302 | ||||||
| chr16:15693617
|
A | G | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-548A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693617 | ||||||
| chr16:15693677
|
C | T | 3 | a0001c0001t0008g0359a0001c0001t0008g0360a0001c0001t0008g0361 | 3 | HG02622.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.704-488C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693677 | ||||||
| chr16:15693678
|
G | A | 2 | a0001c0001t0006g0104a0001c0001t0006g0106 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.704-487G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693678 | ||||||
| chr16:15693738
|
G | A | 1 | a0001c0001t0029g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704-427G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693738 | ||||||
| chr16:15693762
|
G | A | 19 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.704-403G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693762 | ||||||
| chr16:15693854
|
C | T | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.704-311C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693854 | ||||||
| chr16:15693994
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.704-171C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693994 | ||||||
| chr16:15694084
|
G | A | 1 | a0001c0001t0010g0103 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.704-81G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15694084 | ||||||
| chr16:15694369
|
A | C | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+113A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694369 | ||||||
| chr16:15694623
|
C | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.795+367C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694623 | ||||||
| chr16:15694838
|
G | C | 37 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(34): Show | 37 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.795+582G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694838 | ||||||
| chr16:15694980
|
G | A | 129 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(126): Show | 129 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.795+724G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694980 | ||||||
| chr16:15695078
|
G | A | 19 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.795+822G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695078 | ||||||
| chr16:15695173
|
C | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.795+917C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695173 | ||||||
| chr16:15695203
|
C | CT | 24 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0044others(21): Show | 24 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.795+971dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
C | CTT | 10 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0007g0323others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+970_795+971dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+963_795+971dup others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0008g0351a0001c0001t0008g0359a0001c0001t0008g0360others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.795+962_795+971dup others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0008g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795+961_795+971dup others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
CT | C | 70 | a0001c0001t0001g0026a0001c0001t0001g0347a0001c0001t0002g0252others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.795+971delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
CTT | C | 7 | a0001c0001t0003g0001a0001c0001t0003g0128a0001c0001t0003g0141others(4): Show | 8 | HG00544.hp1 HG00642.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+970_795+971del others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0016g0016a0001c0001t0023g0014 | 2 | HG02040.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.795+962_795+971del others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695203
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0016g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.795+961_795+971del others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | |||||
| chr16:15695263
|
T | G | 1 | a0001c0001t0003g0123 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.795+1007T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695263 | ||||||
| chr16:15695274
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.795+1018G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695274 | ||||||
| chr16:15695432
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+1176C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695432 | ||||||
| chr16:15695433
|
G | C | 63 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(60): Show | 64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.795+1177G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695433 | ||||||
| chr16:15695495
|
C | CA | 10 | a0001c0001t0002g0235a0001c0001t0002g0237a0001c0001t0002g0238others(7): Show | 10 | HG01255.hp2 HG03942.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.796-1194dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | |||||
| chr16:15695495
|
CA | C | 72 | a0001c0001t0001g0094a0001c0001t0001g0347a0001c0001t0002g0012others(69): Show | 72 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.796-1194delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | |||||
| chr16:15695495
|
CAA | C | 188 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(185): Show | 189 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.796-1195_796-1194d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | |||||
| chr16:15695626
|
A | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0288a0001c0001t0001g0290others(8): Show | 11 | HG00639.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-1083A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695626 | ||||||
| chr16:15695855
|
A | G | 1 | a0001c0001t0002g0338 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.796-854A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695855 | ||||||
| chr16:15695891
|
T | G | 63 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(60): Show | 64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.796-818T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695891 | ||||||
| chr16:15695950
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.796-759G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695950 | ||||||
| chr16:15696027
|
AT | A | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.796-676delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696027 | |||||
| chr16:15696048
|
AT | A | 177 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0026others(174): Show | 177 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.796-645delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696048 | |||||
| chr16:15696048
|
ATT | A | 26 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.796-646_796-645del others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696048 | |||||
| chr16:15696121
|
T | TGCTTGAG others(7): Show |
269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.796-587_796-586ins others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696121 | |||||
| chr16:15696152
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.796-557T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696152 | ||||||
| chr16:15696174
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.796-535T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696174 | ||||||
| chr16:15696192
|
TAAAA | T | 13 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.796-512_796-509del others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696192 | |||||
| chr16:15696252
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0288a0001c0001t0001g0289others(17): Show | 20 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.796-457A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696252 | ||||||
| chr16:15696289
|
T | C | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0091 | 3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.796-420T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696289 | ||||||
| chr16:15696386
|
C | CA | 105 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.796-312dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696386 | |||||
| chr16:15696390
|
A | AC | 23 | a0001c0001t0001g0013a0001c0001t0001g0196a0001c0001t0001g0287others(20): Show | 23 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.796-319_796-318ins others(1): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696390 | ||||||
| chr16:15696391
|
A | C | 2 | a0001c0001t0002g0012a0001c0001t0002g0039 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.796-318A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696391 | ||||||
| chr16:15696471
|
C | T | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.796-238C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696471 | ||||||
| chr16:15696602
|
C | T | 1 | a0001c0001t0002g0338 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.796-107C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696602 | ||||||
| chr16:15696632
|
G | A | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0302others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-77G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696632 | ||||||
| chr16:15696686
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18980.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.796-23G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696686 | ||||||
| chr16:15697105
|
A | G | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+245A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697105 | ||||||
| chr16:15697134
|
C | G | 1 | a0001c0001t0006g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.947+274C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697134 | ||||||
| chr16:15697189
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.947+329C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697189 | ||||||
| chr16:15697280
|
T | C | 52 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(49): Show | 52 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.947+420T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697280 | ||||||
| chr16:15697312
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.947+452C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697312 | ||||||
| chr16:15697380
|
A | G | 1 | a0001c0001t0005g0163 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.947+520A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697380 | ||||||
| chr16:15697386
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.947+526G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697386 | ||||||
| chr16:15697442
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.947+582C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697442 | ||||||
| chr16:15697451
|
G | A | 3 | a0001c0001t0001g0295a0001c0001t0001g0299a0001c0001t0030g0311 | 3 | HG02055.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.947+591G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697451 | ||||||
| chr16:15697504
|
T | C | 2 | a0001c0001t0003g0036a0001c0001t0003g0037 | 2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.947+644T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697504 | ||||||
| chr16:15697706
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0071others(1): Show | 4 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+846C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697706 | ||||||
| chr16:15697710
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0299 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.947+850A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697710 | ||||||
| chr16:15697743
|
A | G | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.947+883A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697743 | ||||||
| chr16:15697767
|
C | T | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+907C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697767 | ||||||
| chr16:15697795
|
GT | G | 6 | a0001c0001t0004g0105a0001c0001t0004g0167a0001c0001t0004g0170others(3): Show | 6 | HG01261.hp2 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+946delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15697795 | |||||
| chr16:15697802
|
T | G | 9 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(6): Show | 9 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+942T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697802 | ||||||
| chr16:15697881
|
A | G | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+1021A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697881 | ||||||
| chr16:15697904
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+1044C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697904 | ||||||
| chr16:15698030
|
G | A | 38 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(35): Show | 38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+1170G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698030 | ||||||
| chr16:15698121
|
C | G | 6 | a0001c0001t0001g0293a0001c0001t0007g0109a0001c0001t0007g0157others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+1261C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698121 | ||||||
| chr16:15698198
|
G | A | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+1338G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698198 | ||||||
| chr16:15698247
|
CAG | C | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+1388_947+1389d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698247 | ||||||
| chr16:15698307
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+1447G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698307 | ||||||
| chr16:15698376
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.947+1516T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698376 | ||||||
| chr16:15698534
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.947+1674A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698534 | ||||||
| chr16:15698677
|
A | G | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+1817A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698677 | ||||||
| chr16:15698729
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.947+1869C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698729 | ||||||
| chr16:15698779
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.947+1919T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698779 | ||||||
| chr16:15698784
|
C | A | 1 | a0001c0001t0001g0330 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.947+1924C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698784 | ||||||
| chr16:15698863
|
GA | G | 7 | a0001c0001t0003g0308a0001c0001t0007g0323a0001c0001t0007g0324others(4): Show | 7 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.947+2016delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15698863 | |||||
| chr16:15698878
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0201 | 2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.947+2018T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698878 | ||||||
| chr16:15698880
|
AT | A | 38 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(35): Show | 38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+2025delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15698880 | |||||
| chr16:15698915
|
T | C | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2055T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698915 | ||||||
| chr16:15699067
|
A | T | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0144 | 3 | HG01106.hp2 HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.947+2207A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699067 | ||||||
| chr16:15699235
|
G | C | 52 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(49): Show | 52 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.947+2375G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699235 | ||||||
| chr16:15699263
|
C | CT | 6 | a0001c0001t0001g0303a0001c0001t0003g0023a0001c0001t0011g0003others(3): Show | 6 | HG01496.hp2 HG02056.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+2416dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | |||||
| chr16:15699263
|
C | CTT | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2415_947+2416d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | |||||
| chr16:15699263
|
CT | C | 51 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(48): Show | 51 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.947+2416delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | |||||
| chr16:15699294
|
C | G | 4 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+2434C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699294 | ||||||
| chr16:15699309
|
G | A | 13 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.947+2449G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699309 | ||||||
| chr16:15699316
|
G | A | 1 | a0001c0001t0016g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.947+2456G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699316 | ||||||
| chr16:15699363
|
G | A | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+2503G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699363 | ||||||
| chr16:15699432
|
G | T | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947+2572G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699432 | ||||||
| chr16:15699480
|
AAAAC | A | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.947+2631_947+2634d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699480 | |||||
| chr16:15699650
|
T | C | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+2790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699650 | ||||||
| chr16:15699653
|
T | C | 1 | a0001c0001t0014g0344 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.947+2793T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699653 | ||||||
| chr16:15699697
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.947+2837T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699697 | ||||||
| chr16:15699758
|
C | T | 38 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(35): Show | 38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+2898C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699758 | ||||||
| chr16:15699780
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.947+2920G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699780 | ||||||
| chr16:15699782
|
C | T | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2922C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699782 | ||||||
| chr16:15699938
|
G | A | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+3078G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699938 | ||||||
| chr16:15699970
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.947+3110G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699970 | ||||||
| chr16:15700012
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.947+3152C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700012 | ||||||
| chr16:15700017
|
C | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+3157C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700017 | ||||||
| chr16:15700088
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.947+3228C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700088 | ||||||
| chr16:15700157
|
C | T | 1 | a0001c0001t0007g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.947+3297C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700157 | ||||||
| chr16:15700398
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0211 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.947+3538C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700398 | ||||||
| chr16:15700437
|
G | C | 1 | a0001c0001t0002g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.947+3577G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700437 | ||||||
| chr16:15700440
|
C | CT | 43 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(40): Show | 43 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.947+3594dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15700440 | |||||
| chr16:15700440
|
C | CTT | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+3593_947+3594d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15700440 | |||||
| chr16:15700528
|
C | T | 233 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(230): Show | 234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.947+3668C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700528 | ||||||
| chr16:15700578
|
A | G | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+3718A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700578 | ||||||
| chr16:15700588
|
A | G | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+3728A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700588 | ||||||
| chr16:15700671
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.947+3811G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700671 | ||||||
| chr16:15700697
|
C | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+3837C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700697 | ||||||
| chr16:15700740
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.947+3880C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700740 | ||||||
| chr16:15700963
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0342 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.947+4103C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700963 | ||||||
| chr16:15701191
|
T | C | 272 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(269): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.947+4331T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701191 | ||||||
| chr16:15701200
|
G | C | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.947+4340G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701200 | ||||||
| chr16:15701218
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.947+4358C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701218 | ||||||
| chr16:15701237
|
CA | C | 240 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(237): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.947+4392delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15701237 | |||||
| chr16:15701256
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+4396G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701256 | ||||||
| chr16:15701316
|
C | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+4456C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701316 | ||||||
| chr16:15701388
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.947+4528C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701388 | ||||||
| chr16:15701407
|
G | T | 1 | a0001c0001t0016g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.947+4547G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701407 | ||||||
| chr16:15701598
|
G | C | 1 | a0001c0001t0002g0256 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.947+4738G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701598 | ||||||
| chr16:15701615
|
T | C | 265 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(262): Show | 266 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.947+4755T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701615 | ||||||
| chr16:15701666
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.947+4806C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701666 | ||||||
| chr16:15701800
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.947+4940C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701800 | ||||||
| chr16:15701802
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.947+4942G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701802 | ||||||
| chr16:15701819
|
G | A | 20 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(17): Show | 20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.947+4959G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701819 | ||||||
| chr16:15702087
|
G | A | 2 | a0001c0001t0005g0164a0001c0001t0005g0165 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.947+5227G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702087 | ||||||
| chr16:15702094
|
A | G | 1 | a0001c0001t0003g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.947+5234A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702094 | ||||||
| chr16:15702119
|
G | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+5259G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702119 | ||||||
| chr16:15702266
|
A | T | 82 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(79): Show | 83 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.947+5406A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702266 | ||||||
| chr16:15702282
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+5422C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702282 | ||||||
| chr16:15702400
|
T | C | 1 | a0001c0001t0007g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.947+5540T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702400 | ||||||
| chr16:15702462
|
C | G | 83 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(80): Show | 84 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.947+5602C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702462 | ||||||
| chr16:15702567
|
C | CA | 21 | a0001c0001t0001g0062a0001c0001t0001g0094a0001c0001t0002g0012others(18): Show | 21 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.947+5709dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702567 | |||||
| chr16:15702570
|
C | A | 365 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(362): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.947+5710C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702570 | ||||||
| chr16:15702581
|
C | CT | 153 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0038others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.947+5729dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702581 | |||||
| chr16:15702581
|
C | CTT | 91 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.947+5728_947+5729d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702581 | |||||
| chr16:15702590
|
A | T | 1 | a0001c0001t0034g0077 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.947+5730A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702590 | ||||||
| chr16:15702711
|
C | T | 112 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.947+5851C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702711 | ||||||
| chr16:15702759
|
G | A | 1 | a0001c0001t0024g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.947+5899G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702759 | ||||||
| chr16:15703103
|
T | C | 12 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+6243T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703103 | ||||||
| chr16:15703129
|
A | G | 2 | a0001c0001t0006g0121a0001c0001t0006g0286 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.947+6269A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703129 | ||||||
| chr16:15703355
|
T | C | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+6495T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703355 | ||||||
| chr16:15703360
|
G | A | 2 | a0001c0002t0001g0216a0001c0002t0001g0329 | 2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.947+6500G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703360 | ||||||
| chr16:15703447
|
C | T | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+6587C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703447 | ||||||
| chr16:15703480
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.947+6620C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703480 | ||||||
| chr16:15703571
|
G | C | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+6711G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703571 | ||||||
| chr16:15703633
|
G | C | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+6773G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703633 | ||||||
| chr16:15703835
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.947+6975G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703835 | ||||||
| chr16:15703925
|
G | GT | 18 | a0001c0001t0002g0339a0001c0001t0008g0348a0001c0001t0008g0349others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+7073dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15703925 | |||||
| chr16:15703954
|
G | T | 3 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0134 | 3 | NA18945.hp2 NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.947+7094G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703954 | ||||||
| chr16:15703986
|
G | C | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+7126G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703986 | ||||||
| chr16:15704114
|
G | A | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.947+7254G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704114 | ||||||
| chr16:15704158
|
G | T | 2 | a0001c0001t0006g0121a0001c0001t0006g0286 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.947+7298G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704158 | ||||||
| chr16:15704238
|
T | C | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+7378T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704238 | ||||||
| chr16:15704353
|
G | T | 195 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(192): Show | 196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.947+7493G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704353 | ||||||
| chr16:15704401
|
AAT | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0091 | 3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.947+7544_947+7545d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15704401 | |||||
| chr16:15704608
|
G | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG01934.hp2 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+7748G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704608 | ||||||
| chr16:15704614
|
A | T | 1 | a0001c0001t0003g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.947+7754A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704614 | ||||||
| chr16:15704619
|
G | A | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+7759G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704619 | ||||||
| chr16:15704633
|
G | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0090others(2): Show | 5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+7773G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704633 | ||||||
| chr16:15704665
|
G | A | 3 | a0001c0001t0016g0015a0001c0001t0016g0016a0001c0001t0023g0014 | 3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+7805G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704665 | ||||||
| chr16:15704764
|
T | A | 1 | a0001c0001t0016g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.947+7904T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704764 | ||||||
| chr16:15704765
|
C | A | 2 | a0001c0001t0009g0358a0001c0001t0016g0015 | 2 | HG02572.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.947+7905C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704765 | ||||||
| chr16:15704943
|
C | T | 11 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG00673.hp2 HG02056.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.947+8083C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704943 | ||||||
| chr16:15704999
|
G | C | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.947+8139G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704999 | ||||||
| chr16:15705106
|
TAGCTGGG others(4): Show |
T | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.947+8247_947+8257d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705106 | ||||||
| chr16:15705125
|
G | A | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8265G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705125 | ||||||
| chr16:15705444
|
A | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.947+8584A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705444 | ||||||
| chr16:15705518
|
G | A | 1 | a0001c0001t0004g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.947+8658G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705518 | ||||||
| chr16:15705545
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.947+8685C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705545 | ||||||
| chr16:15705663
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.947+8803A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705663 | ||||||
| chr16:15705670
|
G | A | 4 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+8810G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705670 | ||||||
| chr16:15705700
|
G | A | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8840G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705700 | ||||||
| chr16:15705728
|
T | A | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8868T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705728 | ||||||
| chr16:15705772
|
G | C | 67 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(64): Show | 67 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.947+8912G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705772 | ||||||
| chr16:15705898
|
T | A | 1 | a0001c0001t0004g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.947+9038T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705898 | ||||||
| chr16:15705971
|
T | C | 269 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(266): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.947+9111T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705971 | ||||||
| chr16:15705984
|
C | CA | 12 | a0001c0001t0001g0212a0001c0001t0002g0217a0001c0001t0002g0230others(9): Show | 12 | HG00597.hp2 HG00741.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9145dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(1): Show |
68 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0203others(65): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.947+9138_947+9145d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(2): Show |
81 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(78): Show | 81 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.947+9137_947+9145d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(3): Show |
37 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0032others(34): Show | 37 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.947+9136_947+9145d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0079others(13): Show | 16 | HG00099.hp1 HG00597.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.947+9135_947+9145d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0038a0001c0001t0008g0361a0001c0001t0032g0019 | 3 | HG02818.hp1 HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.947+9134_947+9145d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0009g0357a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+9133_947+9145d others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0004g0166a0001c0001t0009g0354a0001c0001t0009g0358others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+9132_947+9145d others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(8): Show |
9 | a0001c0001t0004g0105a0001c0001t0004g0167a0001c0001t0004g0173others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+9131_947+9145d others(17): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(9): Show |
18 | a0001c0001t0004g0162a0001c0001t0004g0168a0001c0001t0004g0169others(15): Show | 18 | HG01261.hp2 HG01891.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.947+9130_947+9145d others(18): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0004g0174a0001c0001t0004g0304a0001c0001t0005g0163others(3): Show | 6 | HG01255.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+9129_947+9145d others(19): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0004g0172a0001c0001t0005g0180a0001c0001t0007g0109 | 3 | HG02486.hp2 NA19043.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.947+9128_947+9145d others(20): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0164a0001c0001t0005g0165 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.947+9127_947+9145d others(21): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15705984
|
CA | C | 13 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0064others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.947+9145delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | |||||
| chr16:15706039
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.947+9179G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706039 | ||||||
| chr16:15706046
|
G | C | 69 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(66): Show | 69 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.947+9186G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706046 | ||||||
| chr16:15706170
|
T | C | 270 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.947+9310T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706170 | ||||||
| chr16:15706257
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0064others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+9397A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706257 | ||||||
| chr16:15706287
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.947+9427C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706287 | ||||||
| chr16:15706331
|
C | T | 194 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(191): Show | 195 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.947+9471C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706331 | ||||||
| chr16:15706340
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.947+9480G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706340 | ||||||
| chr16:15706404
|
GGT | G | 12 | a0001c0001t0002g0220a0001c0001t0002g0270a0001c0001t0002g0314others(9): Show | 12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9545_947+9546d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706404 | ||||||
| chr16:15706408
|
C | A | 12 | a0001c0001t0002g0220a0001c0001t0002g0270a0001c0001t0002g0314others(9): Show | 12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9548C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706408 | ||||||
| chr16:15706412
|
CCCTG | C | 12 | a0001c0001t0002g0220a0001c0001t0002g0270a0001c0001t0002g0314others(9): Show | 12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9553_947+9556d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706412 | ||||||
| chr16:15706563
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.947+9703C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706563 | ||||||
| chr16:15706564
|
G | T | 2 | a0001c0001t0012g0312a0001c0001t0012g0313 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.947+9704G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706564 | ||||||
| chr16:15706587
|
A | C | 9 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(6): Show | 9 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+9727A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706587 | ||||||
| chr16:15706709
|
A | C | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+9849A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706709 | ||||||
| chr16:15706943
|
G | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.947+10083G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706943 | ||||||
| chr16:15707069
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.947+10209C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707069 | ||||||
| chr16:15707098
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.947+10238G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707098 | ||||||
| chr16:15707247
|
G | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.947+10387G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707247 | ||||||
| chr16:15707348
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.947+10488G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707348 | ||||||
| chr16:15707568
|
T | G | 1 | a0001c0001t0002g0339 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.947+10708T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707568 | ||||||
| chr16:15707573
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.947+10713T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707573 | ||||||
| chr16:15707625
|
G | T | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+10765G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707625 | ||||||
| chr16:15707729
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0211 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.947+10869G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707729 | ||||||
| chr16:15707745
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.947+10885G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707745 | ||||||
| chr16:15707756
|
G | T | 1 | a0001c0001t0003g0120 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.947+10896G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707756 | ||||||
| chr16:15707827
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.947+10967C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707827 | ||||||
| chr16:15707832
|
C | T | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+10972C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707832 | ||||||
| chr16:15707841
|
G | C | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+10981G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707841 | ||||||
| chr16:15707937
|
A | G | 15 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(12): Show | 15 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.947+11077A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707937 | ||||||
| chr16:15707959
|
CA | C | 87 | a0001c0001t0001g0257a0001c0001t0002g0012a0001c0001t0002g0039others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.947+11119delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | |||||
| chr16:15707959
|
CAA | C | 52 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0058others(49): Show | 52 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.947+11118_947+1111 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | |||||
| chr16:15707959
|
CAAA | C | 175 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 175 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.947+11117_947+1111 others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | |||||
| chr16:15707978
|
A | C | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+11118A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707978 | ||||||
| chr16:15707978
|
AAG | A | 12 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(9): Show | 12 | HG01261.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.947+11119_947+1112 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707978 | ||||||
| chr16:15707979
|
AG | A | 6 | a0001c0001t0004g0172a0001c0001t0004g0174a0001c0001t0004g0181others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+11120delG | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707979 | ||||||
| chr16:15708006
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+11146C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708006 | ||||||
| chr16:15708153
|
C | T | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.947+11293C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708153 | ||||||
| chr16:15708225
|
C | T | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947+11365C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708225 | ||||||
| chr16:15708292
|
G | A | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+11432G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708292 | ||||||
| chr16:15708351
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0090others(2): Show | 5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+11491G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708351 | ||||||
| chr16:15708423
|
G | T | 1 | a0001c0003t0006g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.947+11563G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708423 | ||||||
| chr16:15708477
|
C | T | 203 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(200): Show | 205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.947+11617C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708477 | ||||||
| chr16:15708747
|
CAGAAA | C | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+11893_947+1189 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15708747 | |||||
| chr16:15709089
|
G | T | 238 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(235): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.947+12229G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709089 | ||||||
| chr16:15709121
|
T | C | 10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.947+12261T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709121 | ||||||
| chr16:15709414
|
A | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+12554A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709414 | ||||||
| chr16:15709503
|
C | T | 1 | a0001c0001t0018g0227 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.947+12643C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709503 | ||||||
| chr16:15709606
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0331 | 2 | HG00735.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.947+12746C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709606 | ||||||
| chr16:15709610
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0061others(17): Show | 20 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.947+12750C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709610 | ||||||
| chr16:15709807
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.947+12947A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709807 | ||||||
| chr16:15709831
|
G | C | 1 | a0001c0001t0008g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.947+12971G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709831 | ||||||
| chr16:15709877
|
C | G | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+13017C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709877 | ||||||
| chr16:15710108
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.947+13248T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710108 | ||||||
| chr16:15710123
|
C | T | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+13263C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710123 | ||||||
| chr16:15710179
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.947+13319C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710179 | ||||||
| chr16:15710311
|
A | G | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+13451A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710311 | ||||||
| chr16:15710319
|
G | A | 14 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0005g0163others(11): Show | 14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.947+13459G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710319 | ||||||
| chr16:15710391
|
C | T | 3 | a0001c0001t0014g0344a0001c0001t0014g0345a0001c0001t0014g0346 | 3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.947+13531C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710391 | ||||||
| chr16:15710427
|
A | G | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+13567A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710427 | ||||||
| chr16:15710469
|
C | T | 4 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(1): Show | 4 | NA18998.hp2 NA19009.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+13609C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710469 | ||||||
| chr16:15710503
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0090others(2): Show | 5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+13643G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710503 | ||||||
| chr16:15710531
|
TAAAAA | T | 7 | a0001c0001t0001g0289a0001c0001t0001g0292a0001c0001t0001g0294others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-13659_948-1365 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710531 | ||||||
| chr16:15710669
|
C | G | 1 | a0001c0001t0004g0183 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.948-13522C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710669 | ||||||
| chr16:15710695
|
T | G | 22 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(19): Show | 22 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-13496T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710695 | ||||||
| chr16:15710699
|
G | T | 235 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(232): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.948-13492G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710699 | ||||||
| chr16:15710834
|
C | T | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-13357C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710834 | ||||||
| chr16:15710873
|
T | C | 11 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(8): Show | 11 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.948-13318T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710873 | ||||||
| chr16:15710967
|
C | T | 27 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(24): Show | 27 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-13224C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710967 | ||||||
| chr16:15711008
|
C | T | 1 | a0001c0001t0006g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.948-13183C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711008 | ||||||
| chr16:15711107
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02155.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-13084G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711107 | ||||||
| chr16:15711108
|
C | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-13083C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711108 | ||||||
| chr16:15711120
|
C | T | 1 | a0001c0001t0037g0088 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.948-13071C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711120 | ||||||
| chr16:15711155
|
C | T | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-13036C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711155 | ||||||
| chr16:15711199
|
C | T | 2 | a0001c0001t0006g0121a0001c0001t0006g0286 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.948-12992C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711199 | ||||||
| chr16:15711381
|
G | C | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-12810G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711381 | ||||||
| chr16:15711411
|
C | G | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.948-12780C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711411 | ||||||
| chr16:15711716
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.948-12475C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711716 | ||||||
| chr16:15711722
|
T | G | 48 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.948-12469T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711722 | ||||||
| chr16:15711725
|
G | C | 1 | a0001c0001t0018g0271 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.948-12466G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711725 | ||||||
| chr16:15711786
|
A | T | 3 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.948-12405A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711786 | ||||||
| chr16:15711795
|
C | T | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-12396C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711795 | ||||||
| chr16:15711816
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.948-12375C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711816 | ||||||
| chr16:15711941
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.948-12250C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711941 | ||||||
| chr16:15712066
|
G | T | 1 | a0001c0001t0002g0224 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.948-12125G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712066 | ||||||
| chr16:15712289
|
A | T | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-11902A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712289 | ||||||
| chr16:15712323
|
T | G | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11868T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712323 | ||||||
| chr16:15712344
|
C | T | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-11847C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712344 | ||||||
| chr16:15712346
|
C | T | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-11845C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712346 | ||||||
| chr16:15712373
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0037g0088 | 2 | NA18945.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.948-11818C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712373 | ||||||
| chr16:15712421
|
G | A | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11770G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712421 | ||||||
| chr16:15712477
|
A | G | 33 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(30): Show | 33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.948-11714A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712477 | ||||||
| chr16:15712505
|
A | C | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.948-11686A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712505 | ||||||
| chr16:15712593
|
C | T | 193 | a0001c0001t0001g0257a0001c0001t0002g0012a0001c0001t0002g0039others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.948-11598C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712593 | ||||||
| chr16:15712609
|
T | C | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11582T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712609 | ||||||
| chr16:15712655
|
G | T | 1 | a0003c0004t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.948-11536G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712655 | ||||||
| chr16:15712801
|
C | CTGGCCAT | 119 | a0001c0001t0001g0257a0001c0001t0002g0078a0001c0001t0002g0098others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.948-11388_948-1138 others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712801 | |||||
| chr16:15712872
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.948-11319T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712872 | ||||||
| chr16:15712878
|
TAC | T | 7 | a0001c0001t0002g0098a0001c0001t0002g0252a0001c0001t0002g0254others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11311_948-1131 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712878 | |||||
| chr16:15712881
|
A | AGTTTTTT others(2): Show |
10 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.948-11309_948-1130 others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712881 | |||||
| chr16:15712882
|
G | GTTTT | 11 | a0001c0001t0001g0013a0001c0001t0001g0288a0001c0001t0001g0290others(8): Show | 11 | HG00639.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.948-11299_948-1129 others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTT | 45 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0089others(42): Show | 46 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.948-11300_948-1129 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTT | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0303others(4): Show | 7 | HG00544.hp2 HG02055.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11301_948-1129 others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(2): Show |
8 | a0001c0001t0009g0354a0001c0001t0009g0356a0001c0001t0009g0357others(5): Show | 8 | HG02040.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.948-11304_948-1129 others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(3): Show |
19 | a0001c0001t0004g0105a0001c0001t0004g0167a0001c0001t0004g0170others(16): Show | 19 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-11305_948-1129 others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0008g0359a0001c0001t0008g0362 | 2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.948-11306_948-1129 others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0237 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.948-11307_948-1129 others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0010g0103 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.948-11296_948-1129 others(18): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(8): Show |
23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(20): Show | 23 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(19): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(9): Show |
5 | a0001c0001t0003g0119a0001c0001t0003g0120a0001c0001t0006g0106others(2): Show | 5 | HG00609.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(20): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(11): Show |
5 | a0001c0001t0002g0233a0001c0001t0011g0003a0001c0001t0011g0004others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(22): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0347a0001c0001t0004g0166 | 2 | HG02615.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(25): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(18): Show |
5 | a0001c0001t0004g0169a0001c0001t0004g0183a0001c0001t0004g0184others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(29): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(19): Show |
6 | a0001c0001t0004g0162a0001c0001t0004g0172a0001c0001t0004g0181others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(30): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(20): Show |
3 | a0001c0001t0002g0107a0001c0001t0002g0343a0001c0001t0004g0171 | 3 | HG02280.hp2 NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(31): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(21): Show |
27 | a0001c0001t0002g0078a0001c0001t0002g0098a0001c0001t0002g0217others(24): Show | 27 | HG00597.hp2 HG00621.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(32): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(22): Show |
23 | a0001c0001t0002g0154a0001c0001t0002g0226a0001c0001t0002g0232others(20): Show | 23 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(33): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(23): Show |
17 | a0001c0001t0002g0224a0001c0001t0002g0260a0001c0001t0002g0272others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(34): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(24): Show |
13 | a0001c0001t0002g0220a0001c0001t0002g0229a0001c0001t0002g0231others(10): Show | 13 | HG01175.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(35): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(25): Show |
6 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0273others(3): Show | 6 | HG02004.hp2 NA18979.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(36): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(26): Show |
4 | a0001c0001t0001g0257a0001c0001t0002g0228a0001c0001t0002g0265others(1): Show | 4 | HG00099.hp2 HG00140.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(37): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(27): Show |
1 | a0001c0001t0002g0340 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.948-11296_948-1129 others(38): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(28): Show |
1 | a0001c0001t0002g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.948-11296_948-1129 others(39): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(29): Show |
4 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0315others(1): Show | 4 | HG01934.hp1 NA18965.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(40): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712882
|
G | GTTTTTTT others(32): Show |
2 | a0001c0001t0002g0332a0001c0001t0002g0333 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(43): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | |||||
| chr16:15712989
|
A | G | 193 | a0001c0001t0001g0257a0001c0001t0002g0012a0001c0001t0002g0039others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.948-11202A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712989 | ||||||
| chr16:15713061
|
A | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11130A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713061 | ||||||
| chr16:15713220
|
C | T | 8 | a0001c0001t0005g0175a0001c0001t0005g0176a0001c0001t0005g0177others(5): Show | 8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.948-10971C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713220 | ||||||
| chr16:15713280
|
A | C | 33 | a0001c0001t0002g0277a0001c0001t0004g0105a0001c0001t0004g0162others(30): Show | 33 | HG00733.hp1 HG01255.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.948-10911A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713280 | ||||||
| chr16:15713291
|
A | G | 52 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(49): Show | 52 | HG00140.hp2 HG00733.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.948-10900A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713291 | ||||||
| chr16:15713295
|
TGAG | T | 27 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.948-10894_948-1089 others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15713295 | |||||
| chr16:15713318
|
G | A | 20 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(17): Show | 20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-10873G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713318 | ||||||
| chr16:15713409
|
A | G | 5 | a0001c0001t0001g0289a0001c0001t0001g0294a0001c0001t0001g0298others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-10782A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713409 | ||||||
| chr16:15713597
|
C | A | 17 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.948-10594C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713597 | ||||||
| chr16:15713601
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.948-10590T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713601 | ||||||
| chr16:15713614
|
G | C | 5 | a0001c0001t0009g0354a0001c0001t0009g0355a0001c0001t0009g0356others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-10577G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713614 | ||||||
| chr16:15713684
|
G | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0064others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-10507G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713684 | ||||||
| chr16:15713820
|
T | C | 118 | a0001c0001t0002g0078a0001c0001t0002g0098a0001c0001t0002g0107others(115): Show | 118 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.948-10371T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713820 | ||||||
| chr16:15713863
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.948-10328G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713863 | ||||||
| chr16:15714027
|
C | T | 4 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0139others(1): Show | 4 | HG02129.hp2 NA18949.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-10164C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714027 | ||||||
| chr16:15714078
|
C | T | 31 | a0001c0001t0003g0001a0001c0001t0003g0126a0001c0001t0003g0127others(28): Show | 32 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-10113C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714078 | ||||||
| chr16:15714166
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0033others(24): Show | 27 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-10025C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714166 | ||||||
| chr16:15714201
|
G | A | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-9990G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714201 | ||||||
| chr16:15714218
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0341 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.948-9973C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714218 | ||||||
| chr16:15714294
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0211 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.948-9897G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714294 | ||||||
| chr16:15714470
|
G | A | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-9721G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714470 | ||||||
| chr16:15714582
|
G | C | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.948-9609G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714582 | ||||||
| chr16:15714689
|
G | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-9502G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714689 | ||||||
| chr16:15714727
|
C | G | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.948-9464C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714727 | ||||||
| chr16:15714774
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.948-9417A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714774 | ||||||
| chr16:15714849
|
G | A | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-9342G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714849 | ||||||
| chr16:15714999
|
T | C | 2 | a0001c0001t0003g0001a0001c0001t0003g0148 | 3 | HG02135.hp1 NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.948-9192T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714999 | ||||||
| chr16:15715115
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-9076G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715115 | ||||||
| chr16:15715119
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-9072G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715119 | ||||||
| chr16:15715260
|
C | T | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-8931C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715260 | ||||||
| chr16:15715320
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.948-8871C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715320 | ||||||
| chr16:15715426
|
T | C | 1 | a0001c0001t0006g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.948-8765T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715426 | ||||||
| chr16:15715497
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-8694C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715497 | ||||||
| chr16:15715550
|
G | A | 2 | a0001c0001t0008g0350a0001c0001t0008g0351 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.948-8641G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715550 | ||||||
| chr16:15715562
|
G | C | 1 | a0001c0001t0003g0146 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.948-8629G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715562 | ||||||
| chr16:15715684
|
G | T | 1 | a0001c0001t0009g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.948-8507G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715684 | ||||||
| chr16:15715692
|
A | G | 2 | a0001c0001t0016g0015a0001c0001t0023g0014 | 2 | HG02040.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.948-8499A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715692 | ||||||
| chr16:15715697
|
T | G | 1 | a0003c0004t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.948-8494T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715697 | ||||||
| chr16:15715972
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.948-8219C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715972 | ||||||
| chr16:15716013
|
G | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.948-8178G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716013 | ||||||
| chr16:15716014
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.948-8177C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716014 | ||||||
| chr16:15716081
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-8110A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716081 | ||||||
| chr16:15716124
|
T | G | 22 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(19): Show | 22 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-8067T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716124 | ||||||
| chr16:15716201
|
G | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0258 | 2 | HG03225.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.948-7990G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716201 | ||||||
| chr16:15716354
|
G | A | 88 | a0001c0001t0002g0078a0001c0001t0002g0098a0001c0001t0002g0107others(85): Show | 88 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.948-7837G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716354 | ||||||
| chr16:15716410
|
A | G | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-7781A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716410 | ||||||
| chr16:15716445
|
C | G | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-7746C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716445 | ||||||
| chr16:15716445
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0090others(2): Show | 5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-7746C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716445 | ||||||
| chr16:15716524
|
G | T | 136 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0090others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.948-7667G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716524 | ||||||
| chr16:15716524
|
GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-7658_948-7649d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15716524 | |||||
| chr16:15716616
|
C | T | 1 | a0001c0001t0007g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.948-7575C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716616 | ||||||
| chr16:15716617
|
G | A | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-7574G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716617 | ||||||
| chr16:15716662
|
T | C | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-7529T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716662 | ||||||
| chr16:15716742
|
G | C | 5 | a0001c0001t0007g0109a0001c0001t0007g0157a0001c0001t0007g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-7449G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716742 | ||||||
| chr16:15716793
|
C | T | 1 | a0001c0001t0004g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.948-7398C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716793 | ||||||
| chr16:15716827
|
G | T | 6 | a0001c0001t0007g0323a0001c0001t0007g0324a0001c0001t0007g0325others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-7364G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716827 | ||||||
| chr16:15716872
|
G | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-7319G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716872 | ||||||
| chr16:15716915
|
T | G | 1 | a0001c0001t0003g0128 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.948-7276T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716915 | ||||||
| chr16:15716957
|
G | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0256 | 2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.948-7234G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716957 | ||||||
| chr16:15717025
|
G | C | 19 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(16): Show | 19 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-7166G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717025 | ||||||
| chr16:15717043
|
C | G | 1 | a0001c0002t0001g0329 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.948-7148C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717043 | ||||||
| chr16:15717166
|
C | T | 128 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(125): Show | 128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.948-7025C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717166 | ||||||
| chr16:15717205
|
C | T | 128 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(125): Show | 128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.948-6986C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717205 | ||||||
| chr16:15717274
|
G | A | 22 | a0001c0001t0001g0013a0001c0001t0001g0287a0001c0001t0001g0288others(19): Show | 22 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-6917G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717274 | ||||||
| chr16:15717314
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-6877C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717314 | ||||||
| chr16:15717351
|
G | C | 1 | a0001c0001t0002g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.948-6840G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717351 | ||||||
| chr16:15717397
|
G | C | 15 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(12): Show | 15 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.948-6794G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717397 | ||||||
| chr16:15717401
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.948-6790G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717401 | ||||||
| chr16:15717546
|
G | A | 2 | a0001c0001t0018g0227a0001c0001t0018g0271 | 2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.948-6645G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717546 | ||||||
| chr16:15717571
|
A | G | 51 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(48): Show | 51 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.948-6620A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717571 | ||||||
| chr16:15717620
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-6571C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717620 | ||||||
| chr16:15717652
|
G | A | 2 | a0001c0002t0001g0191a0001c0002t0001g0192 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.948-6539G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717652 | ||||||
| chr16:15717805
|
G | A | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-6386G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717805 | ||||||
| chr16:15717833
|
A | C | 1 | a0001c0001t0002g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.948-6358A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717833 | ||||||
| chr16:15717965
|
C | T | 1 | a0001c0001t0005g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.948-6226C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717965 | ||||||
| chr16:15718046
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.948-6145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718046 | ||||||
| chr16:15718072
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.948-6119G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718072 | ||||||
| chr16:15718239
|
G | A | 19 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(16): Show | 19 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-5952G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718239 | ||||||
| chr16:15718333
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-5858G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718333 | ||||||
| chr16:15718334
|
A | C | 1 | a0001c0001t0002g0228 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-5857A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718334 | ||||||
| chr16:15718452
|
G | A | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-5739G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718452 | ||||||
| chr16:15718497
|
C | A | 2 | a0001c0001t0002g0250a0001c0001t0002g0334 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.948-5694C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718497 | ||||||
| chr16:15718693
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-5498C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718693 | ||||||
| chr16:15718761
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.948-5430C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718761 | ||||||
| chr16:15718768
|
G | A | 1 | a0001c0001t0002g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.948-5423G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718768 | ||||||
| chr16:15718799
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | NA18959.hp2 NA19004.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-5392A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718799 | ||||||
| chr16:15718899
|
A | G | 18 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-5292A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718899 | ||||||
| chr16:15718925
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.948-5266C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718925 | ||||||
| chr16:15719116
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.948-5075A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719116 | ||||||
| chr16:15719134
|
A | C | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-5057A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719134 | ||||||
| chr16:15719138
|
A | T | 1 | a0001c0001t0035g0209 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.948-5053A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719138 | ||||||
| chr16:15719150
|
G | A | 1 | a0001c0001t0002g0200 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.948-5041G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719150 | ||||||
| chr16:15719156
|
C | T | 1 | a0001c0001t0031g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.948-5035C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719156 | ||||||
| chr16:15719159
|
G | A | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-5032G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719159 | ||||||
| chr16:15719233
|
T | G | 1 | a0001c0001t0003g0308 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.948-4958T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719233 | ||||||
| chr16:15719354
|
G | T | 102 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.948-4837G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719354 | ||||||
| chr16:15719541
|
G | A | 13 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(10): Show | 13 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.948-4650G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719541 | ||||||
| chr16:15719600
|
G | T | 1 | a0001c0001t0002g0244 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.948-4591G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719600 | ||||||
| chr16:15719776
|
G | A | 193 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(190): Show | 194 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.948-4415G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719776 | ||||||
| chr16:15719860
|
A | T | 1 | a0001c0001t0003g0146 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.948-4331A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719860 | ||||||
| chr16:15719874
|
G | A | 2 | a0001c0001t0002g0277a0001c0001t0027g0280 | 2 | HG00733.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.948-4317G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719874 | ||||||
| chr16:15719909
|
C | A | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-4282C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719909 | ||||||
| chr16:15719947
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.948-4244C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719947 | ||||||
| chr16:15720071
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.948-4120G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720071 | ||||||
| chr16:15720088
|
C | T | 239 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(236): Show | 240 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.948-4103C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720088 | ||||||
| chr16:15720265
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.948-3926G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720265 | ||||||
| chr16:15720420
|
A | G | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-3771A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720420 | ||||||
| chr16:15720587
|
G | GA | 40 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0002g0236others(37): Show | 41 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.948-3589dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720587 | |||||
| chr16:15720587
|
GA | G | 16 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(13): Show | 16 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.948-3589delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720587 | |||||
| chr16:15720613
|
A | G | 32 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(29): Show | 32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-3578A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720613 | ||||||
| chr16:15720625
|
G | A | 2 | a0001c0001t0002g0277a0001c0001t0004g0183 | 2 | HG00733.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.948-3566G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720625 | ||||||
| chr16:15720723
|
ACT | A | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-3465_948-3464d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720723 | |||||
| chr16:15720738
|
A | G | 3 | a0001c0001t0004g0162a0001c0001t0004g0168a0001c0001t0004g0174 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.948-3453A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720738 | ||||||
| chr16:15720742
|
T | TAAAAA | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3446_948-3445i others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720742 | |||||
| chr16:15720742
|
TAAAG | T | 38 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(35): Show | 39 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.948-3445_948-3442d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720742 | |||||
| chr16:15720770
|
A | G | 1 | a0001c0001t0038g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.948-3421A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720770 | ||||||
| chr16:15720825
|
C | G | 1 | a0001c0001t0003g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.948-3366C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720825 | ||||||
| chr16:15720835
|
G | A | 1 | a0001c0001t0030g0311 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.948-3356G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720835 | ||||||
| chr16:15721027
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.948-3164G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721027 | ||||||
| chr16:15721064
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-3127C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721064 | ||||||
| chr16:15721080
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3111A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721080 | ||||||
| chr16:15721191
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3000A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721191 | ||||||
| chr16:15721214
|
C | G | 1 | a0001c0001t0001g0347 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-2977C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721214 | ||||||
| chr16:15721320
|
C | T | 1 | a0001c0001t0029g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.948-2871C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721320 | ||||||
| chr16:15721403
|
A | G | 8 | a0001c0001t0005g0175a0001c0001t0005g0176a0001c0001t0005g0177others(5): Show | 8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.948-2788A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721403 | ||||||
| chr16:15721478
|
T | C | 1 | a0001c0001t0032g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-2713T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721478 | ||||||
| chr16:15721494
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0071others(1): Show | 4 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-2697G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721494 | ||||||
| chr16:15721762
|
G | GCTATGGG others(26): Show |
1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-2426_948-2394d others(35): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15721762 | |||||
| chr16:15721765
|
A | G | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-2426A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721765 | ||||||
| chr16:15721921
|
A | G | 7 | a0001c0001t0006g0121a0001c0001t0006g0286a0001c0001t0007g0109others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-2270A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721921 | ||||||
| chr16:15722090
|
C | G | 5 | a0001c0001t0001g0347a0001c0001t0011g0003a0001c0001t0011g0004others(2): Show | 5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-2101C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722090 | ||||||
| chr16:15722254
|
G | C | 14 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-1937G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722254 | ||||||
| chr16:15722289
|
T | C | 272 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(269): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.948-1902T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722289 | ||||||
| chr16:15722520
|
G | A | 39 | a0001c0001t0002g0252a0001c0001t0003g0001a0001c0001t0003g0022others(36): Show | 40 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.948-1671G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722520 | ||||||
| chr16:15722801
|
C | T | 4 | a0001c0001t0011g0003a0001c0001t0011g0004a0001c0001t0011g0005others(1): Show | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-1390C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722801 | ||||||
| chr16:15722831
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.948-1360C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722831 | ||||||
| chr16:15723024
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0193a0001c0001t0001g0199others(5): Show | 8 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.948-1167G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723024 | ||||||
| chr16:15723067
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.948-1124C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723067 | ||||||
| chr16:15723089
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.948-1102A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723089 | ||||||
| chr16:15723175
|
A | C | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-1016A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723175 | ||||||
| chr16:15723192
|
C | A | 3 | a0001c0001t0003g0111a0001c0001t0003g0118a0001c0001t0003g0120 | 3 | HG00408.hp2 NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.948-999C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723192 | ||||||
| chr16:15723315
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-876C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723315 | ||||||
| chr16:15723316
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-875A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723316 | ||||||
| chr16:15723333
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-858A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723333 | ||||||
| chr16:15723338
|
G | C | 85 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.948-853G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723338 | ||||||
| chr16:15723356
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-835A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723356 | ||||||
| chr16:15723367
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-824C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723367 | ||||||
| chr16:15723368
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-823C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723368 | ||||||
| chr16:15723389
|
A | G | 1 | a0001c0001t0002g0224 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.948-802A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723389 | ||||||
| chr16:15723401
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-790C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723401 | ||||||
| chr16:15723414
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-777A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723414 | ||||||
| chr16:15723417
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-774C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723417 | ||||||
| chr16:15723421
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-770C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723421 | ||||||
| chr16:15723422
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-769A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723422 | ||||||
| chr16:15723426
|
C | A | 1 | a0001c0001t0006g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.948-765C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723426 | ||||||
| chr16:15723426
|
C | T | 1 | a0001c0001t0006g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.948-765C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723426 | ||||||
| chr16:15723436
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-755C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723436 | ||||||
| chr16:15723443
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-748T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723443 | ||||||
| chr16:15723454
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-737C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723454 | ||||||
| chr16:15723470
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-721A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723470 | ||||||
| chr16:15723471
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-720A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723471 | ||||||
| chr16:15723472
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-719C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723472 | ||||||
| chr16:15723473
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-718C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723473 | ||||||
| chr16:15723480
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-711C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723480 | ||||||
| chr16:15723493
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-698A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723493 | ||||||
| chr16:15723508
|
ATAG | A | 12 | a0001c0001t0008g0348a0001c0001t0008g0349a0001c0001t0008g0350others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-681_948-679del others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15723508 | |||||
| chr16:15723522
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-669C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723522 | ||||||
| chr16:15723534
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-657C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723534 | ||||||
| chr16:15723539
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-652T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723539 | ||||||
| chr16:15723543
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-648A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723543 | ||||||
| chr16:15723556
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-635A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723556 | ||||||
| chr16:15723561
|
C | T | 2 | a0001c0001t0002g0332a0001c0001t0002g0333 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.948-630C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723561 | ||||||
| chr16:15723563
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-628C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723563 | ||||||
| chr16:15723565
|
T | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-626T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723565 | ||||||
| chr16:15723584
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-607T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723584 | ||||||
| chr16:15723585
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-606G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723585 | ||||||
| chr16:15723586
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-605C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723586 | ||||||
| chr16:15723589
|
G | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-602G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723589 | ||||||
| chr16:15723607
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-584C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723607 | ||||||
| chr16:15723619
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-572C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723619 | ||||||
| chr16:15723620
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-571T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723620 | ||||||
| chr16:15723621
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-570G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723621 | ||||||
| chr16:15723630
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-561A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723630 | ||||||
| chr16:15723631
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-560G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723631 | ||||||
| chr16:15723632
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-559C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723632 | ||||||
| chr16:15723633
|
T | C | 52 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0040others(49): Show | 52 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.948-558T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723633 | ||||||
| chr16:15723663
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-528A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723663 | ||||||
| chr16:15723664
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-527A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723664 | ||||||
| chr16:15723673
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-518A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723673 | ||||||
| chr16:15723750
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-441C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723750 | ||||||
| chr16:15723755
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-436A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723755 | ||||||
| chr16:15723772
|
T | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0341 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.948-419T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723772 | ||||||
| chr16:15723795
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-396A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723795 | ||||||
| chr16:15723805
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-386C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723805 | ||||||
| chr16:15723806
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-385T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723806 | ||||||
| chr16:15723808
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-383A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723808 | ||||||
| chr16:15723839
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-352A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723839 | ||||||
| chr16:15723851
|
T | C | 38 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(35): Show | 38 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.948-340T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723851 | ||||||
| chr16:15723864
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-327A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723864 | ||||||
| chr16:15723865
|
G | C | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-326G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723865 | ||||||
| chr16:15723867
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-324A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723867 | ||||||
| chr16:15723873
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-318T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723873 | ||||||
| chr16:15723875
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-316C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723875 | ||||||
| chr16:15723876
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-315C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723876 | ||||||
| chr16:15723878
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-313T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723878 | ||||||
| chr16:15723879
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-312C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723879 | ||||||
| chr16:15723880
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-311T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723880 | ||||||
| chr16:15723881
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-310T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723881 | ||||||
| chr16:15723885
|
G | C | 1 | a0001c0001t0004g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.948-306G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723885 | ||||||
| chr16:15723890
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-301A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723890 | ||||||
| chr16:15723892
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-299A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723892 | ||||||
| chr16:15723893
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-298C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723893 | ||||||
| chr16:15723894
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-297T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723894 | ||||||
| chr16:15723931
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-260C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723931 | ||||||
| chr16:15723936
|
A | C | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-255A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723936 | ||||||
| chr16:15723937
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-254C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723937 | ||||||
| chr16:15723938
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-253C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723938 | ||||||
| chr16:15723939
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-252C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723939 | ||||||
| chr16:15723940
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-251A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723940 | ||||||
| chr16:15723942
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-249A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723942 | ||||||
| chr16:15723963
|
T | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-228T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723963 | ||||||
| chr16:15723966
|
T | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-225T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723966 | ||||||
| chr16:15723985
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-206C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723985 | ||||||
| chr16:15724004
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-187C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724004 | ||||||
| chr16:15724021
|
A | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-170A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724021 | ||||||
| chr16:15724035
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-156C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724035 | ||||||
| chr16:15724138
|
G | A | 33 | a0001c0001t0004g0105a0001c0001t0004g0162a0001c0001t0004g0166others(30): Show | 33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.948-53G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724138 | ||||||
| chr16:15724151
|
C | T | 1 | a0001c0001t0025g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-40C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724151 |