| geneid | 221294 |
|---|---|
| ensemblid | ENSG00000178425.14 |
| hgncid | 21556 |
| symbol | NT5DC1 |
| name | 5'-nucleotidase domain containing 1 |
| refseq_nuc | NM_152729.3 |
| refseq_prot | NP_689942.2 |
| ensembl_nuc | ENST00000319550.9 |
| ensembl_prot | ENSP00000326858.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 116100853 |
| end | 116249497 |
| strand | + |
| ver | v1.2 |
| region | chr6:116100853-116249497 |
| region5000 | chr6:116095853-116254497 |
| regionname0 | NT5DC1_chr6_116100853_116249497 |
| regionname5000 | NT5DC1_chr6_116095853_116254497 |
| 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 | 1/1 | 455 | 297 | 92 | 55 | 104 | 12 | 32 | 92 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0002 | 0/0 | 455 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0003 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| 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 | 1/1 | 1368 | 296 | 91 | 55 | 104 | 12 | 32 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| c0002 | 0/0 | 1368 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| c0003 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| c0004 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| 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 | 5545 | 87 | 12 | 11 | 46 | 3 | 15 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0002 | 0/0 | 5552 | 57 | 19 | 20 | 9 | 4 | 5 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0003 | 0/1 | 5560 | 41 | 6 | 7 | 27 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0004 | 0/0 | 5562 | 16 | 1 | 3 | 7 | 2 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0005 | 0/0 | 5558 | 10 | 4 | 2 | 0 | 1 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0006 | 0/0 | 5564 | 10 | 4 | 1 | 4 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0007 | 0/0 | 5562 | 10 | 8 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0008 | 0/0 | 5564 | 9 | 1 | 3 | 5 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0009 | 0/0 | 5566 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0010 | 0/0 | 5564 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0011 | 0/0 | 5546 | 4 | 1 | 2 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0012 | 0/0 | 5541 | 4 | 0 | 0 | 4 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0013 | 0/0 | 5554 | 4 | 3 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0014 | 0/0 | 5558 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0015 | 0/0 | 5547 | 2 | 0 | 1 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0016 | 0/0 | 5572 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0017 | 0/0 | 5550 | 2 | 1 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0018 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0019 | 0/0 | 5552 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0020 | 0/0 | 5562 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0021 | 0/0 | 5546 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0022 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0023 | 0/0 | 5543 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0024 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0025 | 0/0 | 5574 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0026 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0027 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0028 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0029 | 0/0 | 5562 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0030 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0031 | 0/0 | 5562 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0032 | 0/0 | 5570 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0033 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0034 | 1/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0035 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0036 | 0/0 | 5564 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0037 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0038 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| t0039 | 0/0 | 5552 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| 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 | 1/1 | 1368 | 296 | 91 | 55 | 104 | 12 | 32 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0003 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0002c0002 | 0/0 | 1368 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0003c0004 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6912 | 87 | 12 | 11 | 46 | 3 | 15 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0002 | 0/0 | 6919 | 54 | 19 | 17 | 9 | 4 | 5 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0003 | 0/1 | 6927 | 41 | 6 | 7 | 27 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0004 | 0/0 | 6929 | 16 | 1 | 3 | 7 | 2 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0005 | 0/0 | 6925 | 10 | 4 | 2 | 0 | 1 | 3 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0006 | 0/0 | 6931 | 10 | 4 | 1 | 4 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0007 | 0/0 | 6929 | 10 | 8 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0008 | 0/0 | 6931 | 9 | 1 | 3 | 5 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0009 | 0/0 | 6933 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0010 | 0/0 | 6931 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0011 | 0/0 | 6913 | 4 | 1 | 2 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0012 | 0/0 | 6908 | 4 | 0 | 0 | 4 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0013 | 0/0 | 6921 | 4 | 3 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0014 | 0/0 | 6925 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0015 | 0/0 | 6914 | 2 | 0 | 1 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0016 | 0/0 | 6939 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0017 | 0/0 | 6917 | 2 | 1 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0018 | 0/0 | 6927 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0019 | 0/0 | 6919 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0020 | 0/0 | 6929 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0021 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0022 | 0/0 | 6912 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0023 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0024 | 0/0 | 6908 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0025 | 0/0 | 6941 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0026 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0027 | 0/0 | 6927 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0028 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0029 | 0/0 | 6929 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0030 | 0/0 | 6933 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0031 | 0/0 | 6929 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0032 | 0/0 | 6937 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0033 | 0/0 | 6918 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0034 | 1/0 | 6919 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0035 | 0/0 | 6933 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0036 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0037 | 0/0 | 6919 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0038 | 0/0 | 6917 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0001t0039 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0001c0003t0014 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0002c0002t0002 | 0/0 | 6919 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| a0003c0004t0002 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | copy fasta | chr6 | 116095853 | 116254497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0015g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0015g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0017g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0017g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0018g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0019g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0019g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0020g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0020g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0021g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0025g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0027g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0028g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0029g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0030g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0031g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0032g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0033g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0034g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0035g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0036g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0037g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0038g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0001t0039g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0001c0003t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| a0003c0004t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | GBR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0216 | EUR | GBR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0164 | EUR | FIN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0137 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0284 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01074 | hp1 | a0001 | c0001 | t0032 | g0243 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01106 | hp2 | a0001 | c0001 | t0029 | g0048 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01168 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01169 | hp2 | a0001 | c0001 | t0011 | g0090 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01175 | hp1 | a0001 | c0001 | t0031 | g0236 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0096 | AMR | PUR | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0249 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01361 | hp1 | a0003 | c0004 | t0002 | g0079 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0253 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0251 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01515 | hp1 | a0001 | c0001 | t0019 | g0149 | EUR | IBS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0103 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0116 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0123 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01934 | hp1 | a0001 | c0001 | t0019 | g0150 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0194 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01993 | hp2 | a0001 | c0001 | t0039 | g0078 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0006 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0276 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0059 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0250 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02451 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02630 | hp2 | a0001 | c0001 | t0026 | g0114 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02683 | hp1 | a0001 | c0001 | t0015 | g0289 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0109 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0062 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02723 | hp2 | a0001 | c0001 | t0024 | g0122 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0213 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02735 | hp2 | a0001 | c0001 | t0020 | g0238 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0247 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0246 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02886 | hp1 | a0001 | c0001 | t0030 | g0113 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0143 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02896 | hp1 | a0001 | c0001 | t0038 | g0141 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0278 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02922 | hp2 | a0001 | c0001 | t0036 | g0135 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0071 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0100 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0115 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03130 | hp1 | a0001 | c0001 | t0033 | g0281 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0244 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0104 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03225 | hp2 | a0001 | c0001 | t0035 | g0292 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0108 | AFR | ESN | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | GWD | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0117 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0232 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03704 | hp2 | a0001 | c0001 | t0021 | g0223 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | PJL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0252 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0262 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0139 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0161 | SAS | STU | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18941 | hp1 | a0001 | c0001 | t0012 | g0173 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18948 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18968 | hp2 | a0001 | c0001 | t0012 | g0171 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18969 | hp2 | a0001 | c0001 | t0028 | g0027 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19004 | hp1 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19007 | hp1 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0029 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19083 | hp2 | a0001 | c0001 | t0012 | g0169 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ASW | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0182 | AFR | ASW | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0128 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20805 | hp2 | a0001 | c0001 | t0017 | g0294 | EUR | TSI | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | GIH | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0270 | AMR | CLM | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | ACB | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | MSL | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| HG06807 | hp2 | a0001 | c0001 | t0037 | g0277 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | USA | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA21309 | hp1 | a0001 | c0003 | t0014 | g0060 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | LWK | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0049 | REF | REF | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0034 | g0142 | REF | REF | NT5DC1_chr6_116095853_116254497 | NT5DC1 | chr6 | 116095853 | 116254497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116106254
|
A | G | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.104A>G | p.Asn35Ser | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/12 | 182/6919 | 104/1368 | 35/455 | chr6 | 116106254 | ||
| chr6:116238243
|
T | G | 1 | a0002 | 2 | HG01168.hp1 HG01192.hp1 |
missense_variant | MODERATE | c.978T>G | p.Ser326Arg | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/12 | 1056/6919 | 978/1368 | 326/455 | chr6 | 116238243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116117881
|
A | G | 1 | a0001c0003 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.465A>G | p.Thr155Thr | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/12 | 543/6919 | 465/1368 | 155/455 | chr6 | 116117881 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116100890
|
C | T | 1 | a0001c0001t0039 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/12 | 41 | chr6 | 116100890 | |||||
| chr6:116244341
|
G | A | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 317 | chr6 | 116244341 | |||||
| chr6:116244562
|
C | A | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(12): Show | 100 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 538 | chr6 | 116244562 | |||||
| chr6:116244799
|
A | G | 2 | a0001c0001t0010a0001c0001t0032 | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*775A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 775 | chr6 | 116244799 | |||||
| chr6:116245033
|
CTATT | C | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1015delTTTA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1012 | INFO_REALIGN_3_PRIME | chr6 | 116245033 | ||||
| chr6:116245042
|
G | A | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(6): Show | 102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1018 | chr6 | 116245042 | |||||
| chr6:116245275
|
G | A | 1 | a0001c0001t0017 | 2 | HG02280.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1251G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1251 | chr6 | 116245275 | |||||
| chr6:116245473
|
C | CA | 2 | a0001c0001t0011a0001c0001t0021 | 5 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1457dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1458 | INFO_REALIGN_3_PRIME | chr6 | 116245473 | ||||
| chr6:116245617
|
A | C | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1593A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1593 | chr6 | 116245617 | |||||
| chr6:116245653
|
G | T | 1 | a0001c0001t0031 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1629 | chr6 | 116245653 | |||||
| chr6:116245682
|
C | T | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*1658C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1658 | chr6 | 116245682 | |||||
| chr6:116245802
|
CT | C | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(6): Show | 102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1780delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1780 | INFO_REALIGN_3_PRIME | chr6 | 116245802 | ||||
| chr6:116245885
|
T | C | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1861T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1861 | chr6 | 116245885 | |||||
| chr6:116246011
|
A | C | 1 | a0001c0001t0030 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1987A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 1987 | chr6 | 116246011 | |||||
| chr6:116246267
|
T | G | 1 | a0001c0001t0033 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2243 | chr6 | 116246267 | |||||
| chr6:116246298
|
C | T | 1 | a0001c0001t0029 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2274C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2274 | chr6 | 116246298 | |||||
| chr6:116246362
|
T | C | 1 | a0001c0001t0017 | 2 | HG02280.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2338T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2338 | chr6 | 116246362 | |||||
| chr6:116246468
|
T | TAC | 2 | a0001c0001t0013a0001c0001t0023 | 5 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470dupAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACAC | 5 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(2): Show | 97 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2467_*2470dupACAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACAC | 4 | a0001c0001t0005a0001c0001t0014a0001c0001t0015others(1): Show | 15 | HG00639.hp1 HG00738.hp1 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2465_*2470dupACAC others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(1): Show |
3 | a0001c0001t0003a0001c0001t0018a0001c0001t0027 | 44 | HG00408.hp2 HG00558.hp2 HG01081.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2463_*2470dupACAC others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(3): Show |
5 | a0001c0001t0004a0001c0001t0007a0001c0001t0020others(2): Show | 30 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2461_*2470dupACAC others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(5): Show |
4 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(1): Show | 27 | HG00642.hp2 HG01496.hp1 HG01884.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2459_*2470dupACAC others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(7): Show |
3 | a0001c0001t0009a0001c0001t0030a0001c0001t0035 | 9 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2457_*2470dupACAC others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(9): Show |
1 | a0001c0001t0026 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2455_*2470dupACAC others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(11): Show |
1 | a0001c0001t0032 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453_*2470dupACAC others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(13): Show |
1 | a0001c0001t0016 | 2 | HG01891.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2451_*2470dupACAC others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
T | TACACACA others(15): Show |
1 | a0001c0001t0025 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2449_*2470dupACAC others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2471 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246468
|
TAC | T | 2 | a0001c0001t0017a0001c0001t0038 | 3 | HG02280.hp1 HG02896.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470delAC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2469 | INFO_REALIGN_3_PRIME | chr6 | 116246468 | ||||
| chr6:116246523
|
A | C | 5 | a0001c0001t0009a0001c0001t0016a0001c0001t0025others(2): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2499A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2499 | chr6 | 116246523 | |||||
| chr6:116246535
|
T | C | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2511T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2511 | chr6 | 116246535 | |||||
| chr6:116246986
|
A | T | 1 | a0001c0001t0020 | 2 | HG02735.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2962A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 2962 | chr6 | 116246986 | |||||
| chr6:116247610
|
A | C | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3586A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3586 | chr6 | 116247610 | |||||
| chr6:116247664
|
T | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3640T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3640 | chr6 | 116247664 | |||||
| chr6:116247752
|
G | T | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3728G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3728 | chr6 | 116247752 | |||||
| chr6:116247821
|
CTT | C | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3798_*3799delTT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 3798 | chr6 | 116247821 | |||||
| chr6:116248123
|
A | C | 1 | a0001c0001t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4099A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4099 | chr6 | 116248123 | |||||
| chr6:116248123
|
A | G | 1 | a0001c0001t0033 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4099 | chr6 | 116248123 | |||||
| chr6:116248138
|
A | C | 5 | a0001c0001t0009a0001c0001t0016a0001c0001t0025others(2): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4114A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4114 | chr6 | 116248138 | |||||
| chr6:116248314
|
G | A | 1 | a0001c0001t0019 | 2 | HG01515.hp1 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4290G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4290 | chr6 | 116248314 | |||||
| chr6:116248770
|
G | A | 5 | a0001c0001t0009a0001c0001t0016a0001c0001t0025others(2): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4746G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4746 | chr6 | 116248770 | |||||
| chr6:116248799
|
A | T | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4775A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 4775 | chr6 | 116248799 | |||||
| chr6:116249173
|
GCTCT | G | 8 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5152_*5155delCTCT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5152 | INFO_REALIGN_3_PRIME | chr6 | 116249173 | ||||
| chr6:116249180
|
A | C | 1 | a0001c0001t0036 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5156 | chr6 | 116249180 | |||||
| chr6:116249275
|
TTTAA | T | 1 | a0001c0001t0012 | 4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5256_*5259delTTAA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5256 | INFO_REALIGN_3_PRIME | chr6 | 116249275 | ||||
| chr6:116249325
|
A | G | 16 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(13): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5301A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5301 | chr6 | 116249325 | |||||
| chr6:116249360
|
C | T | 1 | a0001c0001t0021 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5336 | chr6 | 116249360 | |||||
| chr6:116249434
|
T | C | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(6): Show | 102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5410T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 12/12 | 5410 | chr6 | 116249434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116101118
|
C | G | 56 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(53): Show | 56 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.93+95C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101118 | ||||||
| chr6:116101299
|
T | C | 1 | a0001c0001t0027g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.93+276T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101299 | ||||||
| chr6:116101310
|
T | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0002g0047others(63): Show | 68 | HG00408.hp2 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.93+287T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101310 | ||||||
| chr6:116101371
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0148a0001c0001t0001g0151others(129): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.93+348C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101371 | ||||||
| chr6:116101380
|
A | C | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.93+357A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101380 | ||||||
| chr6:116101446
|
AT | A | 28 | a0001c0001t0001g0075a0001c0001t0002g0004a0001c0001t0002g0063others(25): Show | 29 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+431delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116101446 | |||||
| chr6:116101553
|
A | G | 2 | a0001c0001t0002g0293a0001c0001t0017g0294 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.93+530A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101553 | ||||||
| chr6:116101601
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.93+578A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101601 | ||||||
| chr6:116101684
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(150): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.93+661G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101684 | ||||||
| chr6:116101718
|
G | A | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+695G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101718 | ||||||
| chr6:116101737
|
T | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.93+714T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101737 | ||||||
| chr6:116101765
|
C | A | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.93+742C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116101765 | ||||||
| chr6:116102081
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(216): Show | 223 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.93+1058T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102081 | ||||||
| chr6:116102136
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(218): Show | 225 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.93+1113T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102136 | ||||||
| chr6:116102214
|
GGCACCCG others(9): Show |
G | 12 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(9): Show | 12 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+1198_93+1213del others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116102214 | |||||
| chr6:116102289
|
C | T | 1 | a0001c0001t0031g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.93+1266C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102289 | ||||||
| chr6:116102316
|
A | T | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.93+1293A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102316 | ||||||
| chr6:116102609
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.93+1586A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102609 | ||||||
| chr6:116102628
|
CAA | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+1606_93+1607del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102628 | ||||||
| chr6:116102856
|
G | A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.93+1833G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116102856 | ||||||
| chr6:116103113
|
C | T | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2090C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103113 | ||||||
| chr6:116103321
|
C | CCACTGTT others(23): Show |
2 | a0001c0001t0003g0233a0001c0001t0020g0232 | 2 | HG02132.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.93+2306_93+2335dup others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr6 | 116103321 | |||||
| chr6:116103399
|
C | T | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2376C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103399 | ||||||
| chr6:116103461
|
T | C | 23 | a0001c0001t0001g0148a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.93+2438T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103461 | ||||||
| chr6:116103490
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(173): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.93+2467C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103490 | ||||||
| chr6:116103551
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(176): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.93+2528T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103551 | ||||||
| chr6:116103560
|
C | T | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.93+2537C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103560 | ||||||
| chr6:116103650
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.94-2594A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116103650 | ||||||
| chr6:116104031
|
T | G | 4 | a0001c0001t0002g0047a0001c0001t0003g0049a0001c0001t0004g0050others(1): Show | 4 | HG01099.hp2 HG01106.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-2213T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104031 | ||||||
| chr6:116104165
|
G | A | 9 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-2079G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104165 | ||||||
| chr6:116104253
|
T | C | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.94-1991T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104253 | ||||||
| chr6:116104260
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.94-1984C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104260 | ||||||
| chr6:116104336
|
A | T | 1 | a0001c0001t0035g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-1908A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104336 | ||||||
| chr6:116104442
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(178): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.94-1802T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104442 | ||||||
| chr6:116104443
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.94-1801G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104443 | ||||||
| chr6:116104465
|
A | G | 9 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-1779A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104465 | ||||||
| chr6:116104554
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-1690A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104554 | ||||||
| chr6:116104833
|
T | C | 10 | a0001c0001t0004g0249a0001c0001t0004g0252a0001c0001t0004g0254others(7): Show | 10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.94-1411T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104833 | ||||||
| chr6:116104907
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94-1337G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116104907 | ||||||
| chr6:116105002
|
A | T | 25 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0053others(22): Show | 25 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-1242A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105002 | ||||||
| chr6:116105246
|
C | T | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-998C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105246 | ||||||
| chr6:116105271
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | NA18947.hp2 NA19067.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-973G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105271 | ||||||
| chr6:116105819
|
C | T | 5 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-425C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105819 | ||||||
| chr6:116105870
|
T | G | 1 | a0001c0001t0010g0102 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-374T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116105870 | ||||||
| chr6:116106207
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.94-37G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 1/11 | chr6 | 116106207 | ||||||
| chr6:116106343
|
CT | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0075others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.185+27delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116106343 | |||||
| chr6:116106343
|
CTT | C | 15 | a0001c0001t0001g0156a0001c0001t0002g0047a0001c0001t0002g0051others(12): Show | 15 | HG00741.hp1 HG01069.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.185+26_185+27delTT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116106343 | |||||
| chr6:116106410
|
A | G | 2 | a0001c0001t0009g0144a0001c0001t0014g0143 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.185+75A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106410 | ||||||
| chr6:116106497
|
T | C | 1 | a0001c0001t0029g0048 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.185+162T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106497 | ||||||
| chr6:116106631
|
A | G | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.185+296A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106631 | ||||||
| chr6:116106651
|
G | A | 176 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0119others(173): Show | 180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.185+316G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106651 | ||||||
| chr6:116106983
|
G | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+648G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116106983 | ||||||
| chr6:116107044
|
T | C | 21 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(18): Show | 21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+709T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107044 | ||||||
| chr6:116107274
|
G | A | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+939G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107274 | ||||||
| chr6:116107423
|
C | A | 2 | a0001c0001t0002g0293a0001c0001t0017g0294 | 2 | HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.186-941C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107423 | ||||||
| chr6:116107471
|
C | T | 1 | a0001c0001t0002g0275 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.186-893C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107471 | ||||||
| chr6:116107540
|
T | TTTTTA | 108 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.186-779_186-775dup others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
T | TTTTTATT others(3): Show |
17 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146others(14): Show | 17 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.186-784_186-775dup others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
T | TTTTTATT others(8): Show |
10 | a0001c0001t0002g0111a0001c0001t0003g0112a0001c0001t0009g0107others(7): Show | 10 | HG01884.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-789_186-775dup others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
T | TTTTTATT others(13): Show |
3 | a0001c0001t0002g0106a0001c0001t0010g0102a0001c0001t0010g0244 | 3 | HG02451.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.186-794_186-775dup others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
TTTTTA | T | 46 | a0001c0001t0001g0075a0001c0001t0001g0222a0001c0001t0002g0004others(43): Show | 47 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.186-779_186-775del others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
TTTTTATT others(3): Show |
T | 29 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0053others(26): Show | 29 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.186-784_186-775del others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107540
|
TTTTTATT others(8): Show |
T | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-789_186-775del others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107540 | |||||
| chr6:116107560
|
A | ATTTTCT | 5 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | HG01175.hp2 HG01993.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-800_186-799ins others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107560 | |||||
| chr6:116107642
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-722G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107642 | ||||||
| chr6:116107672
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.186-692A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116107672 | ||||||
| chr6:116107990
|
A | ATG | 3 | a0001c0001t0001g0219a0001c0001t0015g0289a0001c0001t0035g0292 | 3 | HG02683.hp1 HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.186-356_186-355dup others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107990 | |||||
| chr6:116107990
|
ATGTGTGT others(1): Show |
A | 26 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(23): Show | 26 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-362_186-355del others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr6 | 116107990 | |||||
| chr6:116108242
|
A | G | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-122A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 2/11 | chr6 | 116108242 | ||||||
| chr6:116108460
|
T | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(178): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.257+25T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108460 | ||||||
| chr6:116108468
|
A | G | 22 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(19): Show | 22 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.257+33A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108468 | ||||||
| chr6:116108801
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(178): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.257+366A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108801 | ||||||
| chr6:116108812
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.257+377G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116108812 | ||||||
| chr6:116109219
|
G | A | 142 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0119others(139): Show | 146 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.257+784G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109219 | ||||||
| chr6:116109284
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.257+849C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109284 | ||||||
| chr6:116109370
|
G | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(176): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.257+935G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109370 | ||||||
| chr6:116109537
|
A | G | 27 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(24): Show | 27 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.257+1102A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109537 | ||||||
| chr6:116109575
|
T | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.257+1140T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109575 | ||||||
| chr6:116109640
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(178): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.257+1205G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109640 | ||||||
| chr6:116109720
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.258-1130C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109720 | ||||||
| chr6:116109817
|
C | T | 7 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-1033C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109817 | ||||||
| chr6:116109858
|
AAACTACA others(27): Show |
A | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.258-969_258-936del others(34): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr6 | 116109858 | |||||
| chr6:116109877
|
A | G | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.258-973A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109877 | ||||||
| chr6:116109995
|
A | G | 9 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-855A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116109995 | ||||||
| chr6:116110095
|
C | T | 22 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(19): Show | 22 | HG01074.hp1 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-755C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110095 | ||||||
| chr6:116110209
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(178): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.258-641G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110209 | ||||||
| chr6:116110263
|
C | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(176): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.258-587C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110263 | ||||||
| chr6:116110329
|
C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258-521C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110329 | ||||||
| chr6:116110453
|
C | T | 1 | a0001c0001t0031g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.258-397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110453 | ||||||
| chr6:116110706
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258-144A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110706 | ||||||
| chr6:116110740
|
C | A | 1 | a0001c0001t0003g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.258-110C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 3/11 | chr6 | 116110740 | ||||||
| chr6:116111038
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364+82C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111038 | ||||||
| chr6:116111274
|
C | T | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.364+318C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111274 | ||||||
| chr6:116111431
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.364+475A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111431 | ||||||
| chr6:116111473
|
T | G | 23 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.364+517T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111473 | ||||||
| chr6:116111489
|
A | G | 23 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.364+533A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111489 | ||||||
| chr6:116111540
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(155): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.364+584T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111540 | ||||||
| chr6:116111680
|
G | A | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+724G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111680 | ||||||
| chr6:116111826
|
A | G | 7 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0005g0134others(4): Show | 7 | HG00642.hp2 HG02922.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+870A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111826 | ||||||
| chr6:116111861
|
G | C | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.364+905G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111861 | ||||||
| chr6:116111901
|
A | T | 2 | a0001c0001t0001g0217a0001c0001t0020g0232 | 2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.364+945A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116111901 | ||||||
| chr6:116112102
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(152): Show | 157 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.364+1146C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112102 | ||||||
| chr6:116112172
|
G | A | 10 | a0001c0001t0004g0249a0001c0001t0004g0252a0001c0001t0004g0254others(7): Show | 10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+1216G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112172 | ||||||
| chr6:116112383
|
C | A | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+1427C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112383 | ||||||
| chr6:116112475
|
C | T | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.364+1519C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112475 | ||||||
| chr6:116112793
|
A | T | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.364+1837A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112793 | ||||||
| chr6:116112920
|
A | G | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.364+1964A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116112920 | ||||||
| chr6:116113252
|
A | C | 4 | a0001c0001t0002g0293a0001c0001t0005g0280a0001c0001t0008g0147others(1): Show | 4 | HG01981.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+2296A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113252 | ||||||
| chr6:116113454
|
G | A | 23 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.365-2237G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113454 | ||||||
| chr6:116113752
|
G | C | 10 | a0001c0001t0004g0249a0001c0001t0004g0252a0001c0001t0004g0254others(7): Show | 10 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-1939G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113752 | ||||||
| chr6:116113809
|
G | A | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104 | 3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-1882G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116113809 | ||||||
| chr6:116114355
|
A | C | 24 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0054others(21): Show | 24 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1336A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114355 | ||||||
| chr6:116114397
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-1294C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114397 | ||||||
| chr6:116114430
|
C | T | 8 | a0001c0001t0001g0283a0001c0001t0001g0285a0001c0001t0001g0286others(5): Show | 8 | HG00738.hp1 HG01081.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-1261C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114430 | ||||||
| chr6:116114431
|
G | A | 1 | a0001c0001t0006g0005 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.365-1260G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114431 | ||||||
| chr6:116114478
|
T | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365-1213T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114478 | ||||||
| chr6:116114531
|
GGGGGA | G | 22 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(19): Show | 22 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.365-1155_365-1151d others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114531 | |||||
| chr6:116114532
|
GGGGA | G | 58 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0151others(55): Show | 61 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.365-1155_365-1152d others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114532 | |||||
| chr6:116114533
|
GGGA | G | 42 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0002g0004others(39): Show | 43 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.365-1155_365-1153d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116114533 | |||||
| chr6:116114536
|
A | G | 4 | a0001c0001t0005g0280a0001c0001t0007g0246a0001c0001t0014g0247others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-1155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114536 | ||||||
| chr6:116114538
|
G | A | 17 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0054others(14): Show | 17 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.365-1153G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114538 | ||||||
| chr6:116114539
|
G | C | 2 | a0001c0001t0006g0005a0001c0001t0018g0127 | 3 | HG02451.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.365-1152G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114539 | ||||||
| chr6:116114541
|
G | T | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365-1150G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114541 | ||||||
| chr6:116114575
|
T | C | 162 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0075others(159): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.365-1116T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114575 | ||||||
| chr6:116114632
|
C | T | 103 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(100): Show | 107 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.365-1059C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114632 | ||||||
| chr6:116114648
|
G | A | 25 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(22): Show | 25 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.365-1043G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114648 | ||||||
| chr6:116114794
|
G | A | 104 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(101): Show | 108 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.365-897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114794 | ||||||
| chr6:116114854
|
G | A | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.365-837G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114854 | ||||||
| chr6:116114974
|
A | G | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365-717A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116114974 | ||||||
| chr6:116115156
|
G | T | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.365-535G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115156 | ||||||
| chr6:116115234
|
A | ATTTGTC | 198 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0119others(195): Show | 202 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.365-455_365-454ins others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr6 | 116115234 | |||||
| chr6:116115257
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-434A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115257 | ||||||
| chr6:116115370
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.365-321T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115370 | ||||||
| chr6:116115433
|
A | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.365-258A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115433 | ||||||
| chr6:116115679
|
G | T | 1 | a0001c0001t0007g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.365-12G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 4/11 | chr6 | 116115679 | ||||||
| chr6:116115781
|
A | T | 18 | a0001c0001t0003g0007a0001c0001t0003g0288a0001c0001t0004g0157others(15): Show | 18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.444+11A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116115781 | ||||||
| chr6:116115849
|
A | G | 13 | a0001c0001t0001g0282a0001c0001t0003g0291a0001c0001t0006g0005others(10): Show | 14 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+79A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116115849 | ||||||
| chr6:116116124
|
G | A | 52 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(49): Show | 54 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.444+354G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116124 | ||||||
| chr6:116116164
|
G | A | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.444+394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116164 | ||||||
| chr6:116116343
|
T | TAAAAATA others(305): Show |
1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.444+591_444+592ins others(312): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr6 | 116116343 | |||||
| chr6:116116343
|
T | TAAAAATA others(347): Show |
2 | a0001c0001t0001g0121a0001c0001t0024g0122 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.444+591_444+592ins others(354): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr6 | 116116343 | |||||
| chr6:116116365
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.444+595C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116365 | ||||||
| chr6:116116418
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.444+648C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116418 | ||||||
| chr6:116116421
|
A | G | 4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0052others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+651A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116421 | ||||||
| chr6:116116428
|
A | G | 58 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(55): Show | 60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.444+658A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116428 | ||||||
| chr6:116116458
|
A | G | 54 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(51): Show | 56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.444+688A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116458 | ||||||
| chr6:116116566
|
C | T | 2 | a0001c0001t0003g0291a0001c0001t0006g0118 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.444+796C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116566 | ||||||
| chr6:116116709
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.444+939A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116709 | ||||||
| chr6:116116752
|
T | C | 54 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(51): Show | 56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.444+982T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116752 | ||||||
| chr6:116116753
|
G | A | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.444+983G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116753 | ||||||
| chr6:116116877
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-984G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116116877 | ||||||
| chr6:116117151
|
T | C | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-710T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117151 | ||||||
| chr6:116117162
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.445-699A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117162 | ||||||
| chr6:116117199
|
A | G | 58 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(55): Show | 60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.445-662A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117199 | ||||||
| chr6:116117203
|
A | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.445-658A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117203 | ||||||
| chr6:116117242
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.445-619T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117242 | ||||||
| chr6:116117397
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.445-464A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117397 | ||||||
| chr6:116117506
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-355T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117506 | ||||||
| chr6:116117549
|
T | C | 1 | a0001c0001t0004g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445-312T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117549 | ||||||
| chr6:116117600
|
G | A | 1 | a0001c0001t0035g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.445-261G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117600 | ||||||
| chr6:116117602
|
C | G | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.445-259C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117602 | ||||||
| chr6:116117797
|
G | A | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445-64G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 5/11 | chr6 | 116117797 | ||||||
| chr6:116117972
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+27A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116117972 | ||||||
| chr6:116117997
|
G | T | 1 | a0001c0001t0002g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.529+52G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116117997 | ||||||
| chr6:116118015
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.529+70A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118015 | ||||||
| chr6:116118057
|
A | G | 183 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(180): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.529+112A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118057 | ||||||
| chr6:116118155
|
T | C | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+210T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118155 | ||||||
| chr6:116118331
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+386G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118331 | ||||||
| chr6:116118411
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.529+466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118411 | ||||||
| chr6:116118494
|
G | A | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+549G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118494 | ||||||
| chr6:116118581
|
C | CAT | 144 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(141): Show | 148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+637_529+638ins others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116118581 | |||||
| chr6:116118807
|
T | G | 7 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+862T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118807 | ||||||
| chr6:116118844
|
A | C | 58 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(55): Show | 60 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.529+899A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116118844 | ||||||
| chr6:116119031
|
T | C | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+1086T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119031 | ||||||
| chr6:116119047
|
C | T | 15 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0003g0049others(12): Show | 15 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.529+1102C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119047 | ||||||
| chr6:116119048
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+1103G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119048 | ||||||
| chr6:116119657
|
C | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+1712C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119657 | ||||||
| chr6:116119756
|
A | T | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529+1811A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119756 | ||||||
| chr6:116119757
|
A | AT | 12 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(9): Show | 12 | HG01099.hp2 HG01106.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.529+1822dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116119757 | |||||
| chr6:116119758
|
T | A | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529+1813T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119758 | ||||||
| chr6:116119827
|
A | G | 4 | a0001c0001t0002g0047a0001c0001t0003g0049a0001c0001t0004g0050others(1): Show | 4 | HG01099.hp2 HG01106.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+1882A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119827 | ||||||
| chr6:116119916
|
T | C | 2 | a0001c0001t0004g0157a0001c0001t0004g0183 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+1971T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119916 | ||||||
| chr6:116119960
|
C | T | 1 | a0001c0001t0003g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.529+2015C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116119960 | ||||||
| chr6:116120066
|
T | TGGG | 288 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(285): Show | 294 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.529+2122_529+2123i others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116120066 | |||||
| chr6:116120076
|
C | G | 1 | a0001c0001t0001g0222 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.529+2131C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120076 | ||||||
| chr6:116120189
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+2244C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120189 | ||||||
| chr6:116120265
|
A | G | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+2320A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120265 | ||||||
| chr6:116120281
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.529+2336A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120281 | ||||||
| chr6:116120295
|
C | A | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529+2350C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120295 | ||||||
| chr6:116120307
|
C | G | 5 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(2): Show | 5 | HG00738.hp1 HG02258.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+2362C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120307 | ||||||
| chr6:116120483
|
C | G | 77 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0053others(74): Show | 79 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.529+2538C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116120483 | ||||||
| chr6:116121383
|
G | T | 1 | a0001c0001t0006g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.529+3438G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121383 | ||||||
| chr6:116121491
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.529+3546C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121491 | ||||||
| chr6:116121734
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+3789C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121734 | ||||||
| chr6:116121972
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+4027C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116121972 | ||||||
| chr6:116122145
|
A | G | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+4200A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122145 | ||||||
| chr6:116122175
|
A | G | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+4230A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122175 | ||||||
| chr6:116122191
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529+4246A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122191 | ||||||
| chr6:116122221
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.529+4276T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122221 | ||||||
| chr6:116122376
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0184 | 2 | NA18991.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.529+4431G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122376 | ||||||
| chr6:116122385
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.529+4440G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122385 | ||||||
| chr6:116122572
|
T | A | 144 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(141): Show | 148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+4627T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122572 | ||||||
| chr6:116122577
|
C | A | 23 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.529+4632C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122577 | ||||||
| chr6:116122672
|
G | A | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+4727G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122672 | ||||||
| chr6:116122849
|
A | C | 3 | a0001c0001t0016g0116a0001c0001t0016g0117a0001c0001t0025g0115 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+4904A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122849 | ||||||
| chr6:116122901
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.529+4956A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122901 | ||||||
| chr6:116122903
|
A | C | 1 | a0001c0001t0006g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+4958A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122903 | ||||||
| chr6:116122922
|
G | C | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+4977G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122922 | ||||||
| chr6:116122954
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5009G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116122954 | ||||||
| chr6:116123005
|
A | C | 52 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(49): Show | 54 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.529+5060A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123005 | ||||||
| chr6:116123215
|
A | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5270A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123215 | ||||||
| chr6:116123444
|
T | A | 144 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(141): Show | 148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+5499T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123444 | ||||||
| chr6:116123486
|
G | A | 1 | a0001c0001t0003g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.529+5541G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123486 | ||||||
| chr6:116123630
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5685T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123630 | ||||||
| chr6:116123734
|
A | G | 2 | a0001c0001t0003g0014a0001c0001t0003g0041 | 2 | NA18942.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.529+5789A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123734 | ||||||
| chr6:116123922
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+5977G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123922 | ||||||
| chr6:116123990
|
A | G | 23 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(20): Show | 23 | HG01106.hp1 HG01123.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.529+6045A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116123990 | ||||||
| chr6:116124016
|
G | A | 1 | a0001c0003t0014g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+6071G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124016 | ||||||
| chr6:116124106
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529+6161T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124106 | ||||||
| chr6:116124560
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6615A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124560 | ||||||
| chr6:116124733
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.529+6788A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124733 | ||||||
| chr6:116124792
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6847T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124792 | ||||||
| chr6:116124842
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.529+6897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124842 | ||||||
| chr6:116124851
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+6906T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124851 | ||||||
| chr6:116124852
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+6907G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124852 | ||||||
| chr6:116124887
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+6942G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116124887 | ||||||
| chr6:116125009
|
A | G | 1 | a0001c0001t0003g0002 | 2 | NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.529+7064A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125009 | ||||||
| chr6:116125035
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.529+7090A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125035 | ||||||
| chr6:116125143
|
A | G | 1 | a0001c0001t0010g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.529+7198A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125143 | ||||||
| chr6:116125199
|
C | T | 1 | a0001c0001t0004g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.529+7254C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125199 | ||||||
| chr6:116125235
|
G | A | 8 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+7290G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125235 | ||||||
| chr6:116125296
|
A | G | 1 | a0001c0001t0017g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529+7351A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125296 | ||||||
| chr6:116125326
|
C | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+7381C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125326 | ||||||
| chr6:116125413
|
A | G | 144 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0136others(141): Show | 148 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.529+7468A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125413 | ||||||
| chr6:116125470
|
A | C | 2 | a0001c0001t0018g0276a0001c0001t0035g0292 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+7525A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125470 | ||||||
| chr6:116125562
|
AT | A | 9 | a0001c0001t0001g0282a0001c0001t0006g0161a0001c0001t0007g0129others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+7619delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116125562 | |||||
| chr6:116125936
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+7991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125936 | ||||||
| chr6:116125952
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.529+8007C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116125952 | ||||||
| chr6:116126193
|
C | G | 54 | a0001c0001t0001g0075a0001c0001t0001g0282a0001c0001t0002g0004others(51): Show | 56 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.529+8248C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126193 | ||||||
| chr6:116126355
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+8410C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126355 | ||||||
| chr6:116126411
|
A | G | 20 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0003g0049others(17): Show | 20 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.529+8466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126411 | ||||||
| chr6:116126449
|
G | A | 1 | a0001c0001t0006g0005 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+8504G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126449 | ||||||
| chr6:116126799
|
G | T | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+8854G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126799 | ||||||
| chr6:116126859
|
A | G | 5 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+8914A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126859 | ||||||
| chr6:116126859
|
A | T | 2 | a0001c0001t0007g0246a0001c0001t0014g0247 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.529+8914A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126859 | ||||||
| chr6:116126934
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+8989A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126934 | ||||||
| chr6:116126957
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0005g0095a0001c0001t0005g0097others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+9012G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116126957 | ||||||
| chr6:116127117
|
G | T | 1 | a0001c0001t0002g0279 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+9172G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127117 | ||||||
| chr6:116127196
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.529+9251A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127196 | ||||||
| chr6:116127333
|
A | G | 1 | a0001c0001t0002g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+9388A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127333 | ||||||
| chr6:116127480
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+9535A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127480 | ||||||
| chr6:116127813
|
G | A | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+9868G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116127813 | ||||||
| chr6:116128157
|
A | G | 9 | a0001c0001t0001g0282a0001c0001t0006g0161a0001c0001t0007g0129others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+10212A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128157 | ||||||
| chr6:116128185
|
G | T | 1 | a0001c0001t0005g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+10240G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128185 | ||||||
| chr6:116128192
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10247T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128192 | ||||||
| chr6:116128342
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01258.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.529+10397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128342 | ||||||
| chr6:116128393
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529+10448A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128393 | ||||||
| chr6:116128541
|
A | G | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+10596A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128541 | ||||||
| chr6:116128566
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10621T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128566 | ||||||
| chr6:116128720
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.529+10775C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128720 | ||||||
| chr6:116128814
|
G | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+10869G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116128814 | ||||||
| chr6:116129033
|
C | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.529+11088C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129033 | ||||||
| chr6:116129043
|
T | C | 3 | a0001c0001t0020g0232a0001c0001t0020g0238a0001c0001t0032g0243 | 3 | HG01074.hp1 HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+11098T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129043 | ||||||
| chr6:116129153
|
A | T | 3 | a0001c0001t0007g0246a0001c0001t0018g0276a0001c0001t0035g0292 | 3 | HG02145.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+11208A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129153 | ||||||
| chr6:116129252
|
T | C | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+11307T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129252 | ||||||
| chr6:116129515
|
A | G | 4 | a0001c0001t0011g0090a0001c0001t0011g0091a0001c0001t0011g0213others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+11570A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129515 | ||||||
| chr6:116129592
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+11647T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129592 | ||||||
| chr6:116129615
|
C | A | 3 | a0001c0001t0007g0246a0001c0001t0018g0276a0001c0001t0035g0292 | 3 | HG02145.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+11670C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129615 | ||||||
| chr6:116129909
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+11964G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129909 | ||||||
| chr6:116129976
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+12031A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116129976 | ||||||
| chr6:116130050
|
A | G | 14 | a0001c0001t0001g0282a0001c0001t0003g0291a0001c0001t0006g0005others(11): Show | 15 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.529+12105A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130050 | ||||||
| chr6:116130194
|
T | C | 1 | a0001c0001t0003g0012 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.529+12249T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130194 | ||||||
| chr6:116130279
|
A | G | 57 | a0001c0001t0001g0282a0001c0001t0002g0004a0001c0001t0002g0065others(54): Show | 59 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.529+12334A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130279 | ||||||
| chr6:116130339
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+12394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130339 | ||||||
| chr6:116130349
|
T | C | 93 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0053others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.529+12404T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130349 | ||||||
| chr6:116130449
|
G | GT | 21 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(18): Show | 22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+12512dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116130449 | |||||
| chr6:116130553
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.529+12608G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130553 | ||||||
| chr6:116130658
|
T | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+12713T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130658 | ||||||
| chr6:116130703
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0180a0001c0001t0001g0224others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+12758A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130703 | ||||||
| chr6:116130776
|
A | G | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+12831A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130776 | ||||||
| chr6:116130921
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.529+12976G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130921 | ||||||
| chr6:116130991
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13046G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116130991 | ||||||
| chr6:116131040
|
T | G | 150 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0001g0282others(147): Show | 154 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.529+13095T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131040 | ||||||
| chr6:116131106
|
C | T | 2 | a0001c0001t0004g0157a0001c0001t0004g0183 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+13161C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131106 | ||||||
| chr6:116131112
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13167T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131112 | ||||||
| chr6:116131223
|
A | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01258.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.529+13278A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131223 | ||||||
| chr6:116131261
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | NA18947.hp2 NA19067.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+13316G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131261 | ||||||
| chr6:116131270
|
A | G | 1 | a0001c0001t0006g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.529+13325A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131270 | ||||||
| chr6:116131355
|
T | G | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+13410T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131355 | ||||||
| chr6:116131383
|
T | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+13438T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131383 | ||||||
| chr6:116131385
|
T | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+13440T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131385 | ||||||
| chr6:116131398
|
A | G | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+13453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131398 | ||||||
| chr6:116131434
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+13489A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131434 | ||||||
| chr6:116131495
|
C | A | 151 | a0001c0001t0001g0043a0001c0001t0001g0282a0001c0001t0002g0004others(148): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.529+13550C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131495 | ||||||
| chr6:116131870
|
A | G | 1 | a0001c0001t0008g0008 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.529+13925A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131870 | ||||||
| chr6:116131878
|
A | G | 2 | a0001c0001t0019g0149a0001c0001t0019g0150 | 2 | HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.529+13933A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116131878 | ||||||
| chr6:116132003
|
T | A | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.529+14058T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132003 | ||||||
| chr6:116132068
|
T | C | 21 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(18): Show | 22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+14123T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132068 | ||||||
| chr6:116132144
|
G | T | 1 | a0001c0001t0004g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.529+14199G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132144 | ||||||
| chr6:116132666
|
G | C | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+14721G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132666 | ||||||
| chr6:116132805
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529+14860C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132805 | ||||||
| chr6:116132825
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0033g0281 | 3 | HG02074.hp2 HG03130.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.529+14880C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132825 | ||||||
| chr6:116132880
|
A | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+14935A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116132880 | ||||||
| chr6:116133007
|
T | C | 3 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0041 | 3 | NA18942.hp2 NA18983.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.529+15062T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133007 | ||||||
| chr6:116133028
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.529+15083G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133028 | ||||||
| chr6:116133262
|
C | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15317C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133262 | ||||||
| chr6:116133297
|
C | A | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15352C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133297 | ||||||
| chr6:116133425
|
G | A | 198 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0121others(195): Show | 202 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.529+15480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133425 | ||||||
| chr6:116133459
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+15514G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133459 | ||||||
| chr6:116133496
|
C | T | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+15551C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133496 | ||||||
| chr6:116133514
|
C | T | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+15569C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133514 | ||||||
| chr6:116133521
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+15576G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133521 | ||||||
| chr6:116133583
|
C | T | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+15638C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133583 | ||||||
| chr6:116133714
|
G | C | 2 | a0001c0001t0007g0270a0001c0001t0007g0271 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.529+15769G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133714 | ||||||
| chr6:116133768
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+15823A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133768 | ||||||
| chr6:116133823
|
C | G | 1 | a0001c0001t0006g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+15878C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133823 | ||||||
| chr6:116133916
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+15971T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116133916 | ||||||
| chr6:116134239
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+16294A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134239 | ||||||
| chr6:116134385
|
T | A | 91 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(88): Show | 93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+16440T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134385 | ||||||
| chr6:116134490
|
A | C | 1 | a0001c0003t0014g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+16545A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134490 | ||||||
| chr6:116134550
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+16605T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134550 | ||||||
| chr6:116134630
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+16685A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134630 | ||||||
| chr6:116134745
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.529+16800G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134745 | ||||||
| chr6:116134902
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG03654.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.529+16957A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134902 | ||||||
| chr6:116134937
|
A | G | 49 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(46): Show | 50 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.529+16992A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116134937 | ||||||
| chr6:116135052
|
T | C | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+17107T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135052 | ||||||
| chr6:116135172
|
G | A | 154 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(151): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.529+17227G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135172 | ||||||
| chr6:116135341
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17396T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135341 | ||||||
| chr6:116135385
|
AT | A | 4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0052others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17448delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135385 | |||||
| chr6:116135420
|
A | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17475A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135420 | ||||||
| chr6:116135431
|
T | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+17486T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135431 | ||||||
| chr6:116135440
|
C | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+17495C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135440 | ||||||
| chr6:116135441
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17496A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135441 | ||||||
| chr6:116135478
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.529+17533T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135478 | ||||||
| chr6:116135557
|
C | A | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+17612C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135557 | ||||||
| chr6:116135730
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529+17785A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135730 | ||||||
| chr6:116135734
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17789T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135734 | ||||||
| chr6:116135781
|
T | C | 3 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023 | 3 | NA18947.hp1 NA19088.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.529+17836T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135781 | ||||||
| chr6:116135834
|
G | GAT | 33 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0093others(30): Show | 35 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.529+17927_529+1792 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
G | GATAT | 22 | a0001c0001t0001g0094a0001c0001t0001g0136a0001c0001t0001g0148others(19): Show | 22 | HG00741.hp1 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+17925_529+1792 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
G | GATATATA others(3): Show |
4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00558.hp1 HG03704.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17919_529+1792 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
G | GATATATA others(5): Show |
1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.529+17917_529+1792 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
G | GATATATA others(53): Show |
1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529+17903_529+1790 others(64): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GAT | G | 18 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG01175.hp2 HG01346.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+17927_529+1792 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATAT | G | 41 | a0001c0001t0001g0043a0001c0001t0002g0098a0001c0001t0003g0002others(38): Show | 43 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.529+17925_529+1792 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATAT | G | 29 | a0001c0001t0002g0053a0001c0001t0002g0248a0001c0001t0002g0263others(26): Show | 29 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.529+17923_529+1792 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(1): Show |
G | 7 | a0001c0001t0001g0282a0001c0001t0002g0265a0001c0001t0002g0266others(4): Show | 7 | HG02055.hp2 HG04199.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+17921_529+1792 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(3): Show |
G | 3 | a0001c0001t0002g0264a0001c0001t0020g0232a0001c0001t0020g0238 | 3 | HG02735.hp2 HG03654.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.529+17919_529+1792 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(7): Show |
G | 13 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(10): Show | 13 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+17915_529+1792 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(9): Show |
G | 2 | a0001c0001t0001g0222a0001c0001t0009g0107 | 2 | HG02809.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.529+17913_529+1792 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(17): Show |
G | 1 | a0001c0001t0002g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529+17905_529+1792 others(28): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135834
|
GATATATA others(21): Show |
G | 12 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG00438.hp2 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.529+17901_529+1792 others(32): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135834 | |||||
| chr6:116135847
|
A | ATGTATAT others(59): Show |
1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+17903_529+1790 others(70): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135847 | |||||
| chr6:116135847
|
A | ATGTATAT others(55): Show |
1 | a0001c0001t0006g0005 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+17903_529+1790 others(66): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135847 | |||||
| chr6:116135847
|
A | G | 22 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(19): Show | 23 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.529+17902A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135847 | ||||||
| chr6:116135848
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0036g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.529+17905_529+1793 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135848 | |||||
| chr6:116135849
|
A | G | 11 | a0001c0001t0006g0118a0001c0001t0006g0161a0001c0001t0007g0129others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+17904A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135849 | ||||||
| chr6:116135852
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+17907T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135852 | ||||||
| chr6:116135853
|
A | G | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+17908A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135853 | ||||||
| chr6:116135857
|
A | G | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+17912A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135857 | ||||||
| chr6:116135864
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.529+17919T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135864 | ||||||
| chr6:116135864
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0002g0279a0001c0001t0015g0284a0001c0001t0015g0289 | 3 | HG00738.hp1 HG02486.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.529+17921_529+1793 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135864 | |||||
| chr6:116135866
|
T | C | 5 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0005g0134others(2): Show | 5 | HG03239.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+17921T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135866 | ||||||
| chr6:116135866
|
TATATATA others(1): Show |
T | 8 | a0001c0001t0001g0165a0001c0001t0002g0054a0001c0001t0002g0055others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+17923_529+1793 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135866 | |||||
| chr6:116135868
|
T | C | 66 | a0001c0001t0001g0043a0001c0001t0002g0098a0001c0001t0003g0002others(63): Show | 68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.529+17923T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135868 | ||||||
| chr6:116135868
|
TATATAC | T | 4 | a0001c0001t0007g0246a0001c0001t0010g0100a0001c0001t0010g0101others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+17925_529+1793 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135868 | |||||
| chr6:116135870
|
T | C | 89 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(86): Show | 91 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.529+17925T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135870 | ||||||
| chr6:116135870
|
TATAC | T | 15 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 16 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+17927_529+1793 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135870 | |||||
| chr6:116135872
|
T | C | 107 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(104): Show | 109 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.529+17927T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135872 | ||||||
| chr6:116135872
|
T | TATATACA others(5): Show |
1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+17928_529+1792 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135872 | |||||
| chr6:116135872
|
TAC | T | 35 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0177others(32): Show | 35 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.529+17933_529+1793 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116135872 | |||||
| chr6:116135874
|
C | T | 23 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0126others(20): Show | 24 | HG00642.hp1 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+17929C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135874 | ||||||
| chr6:116135880
|
T | C | 1 | a0001c0001t0027g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529+17935T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135880 | ||||||
| chr6:116135884
|
C | T | 1 | a0001c0001t0027g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529+17939C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135884 | ||||||
| chr6:116135903
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.529+17958A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116135903 | ||||||
| chr6:116136099
|
C | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+18154C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136099 | ||||||
| chr6:116136312
|
G | T | 5 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+18367G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136312 | ||||||
| chr6:116136468
|
G | GT | 90 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(87): Show | 92 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.529+18531dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116136468 | |||||
| chr6:116136476
|
T | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+18531T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136476 | ||||||
| chr6:116136511
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.529+18566C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136511 | ||||||
| chr6:116136551
|
G | T | 1 | a0001c0001t0010g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.529+18606G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136551 | ||||||
| chr6:116136767
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+18822G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116136767 | ||||||
| chr6:116137005
|
A | C | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.529+19060A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137005 | ||||||
| chr6:116137254
|
T | C | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+19309T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137254 | ||||||
| chr6:116137807
|
C | T | 2 | a0001c0001t0007g0270a0001c0001t0007g0271 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.529+19862C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137807 | ||||||
| chr6:116137855
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+19910A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137855 | ||||||
| chr6:116137952
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20007G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116137952 | ||||||
| chr6:116138027
|
A | G | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+20082A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138027 | ||||||
| chr6:116138046
|
C | CCCG | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+20104_529+2010 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116138046 | |||||
| chr6:116138048
|
C | T | 5 | a0001c0001t0002g0098a0001c0001t0005g0095a0001c0001t0005g0097others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+20103C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138048 | ||||||
| chr6:116138105
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20160A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138105 | ||||||
| chr6:116138195
|
C | T | 91 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(88): Show | 93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+20250C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138195 | ||||||
| chr6:116138324
|
A | C | 1 | a0001c0001t0035g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.529+20379A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138324 | ||||||
| chr6:116138607
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.529+20662A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138607 | ||||||
| chr6:116138614
|
T | C | 2 | a0001c0001t0003g0024a0001c0001t0003g0046 | 2 | NA18962.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.529+20669T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138614 | ||||||
| chr6:116138703
|
A | G | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+20758A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138703 | ||||||
| chr6:116138772
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+20827T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116138772 | ||||||
| chr6:116139032
|
A | G | 1 | a0001c0001t0004g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.529+21087A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139032 | ||||||
| chr6:116139099
|
A | C | 18 | a0001c0001t0003g0007a0001c0001t0003g0288a0001c0001t0004g0157others(15): Show | 18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+21154A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139099 | ||||||
| chr6:116139101
|
A | C | 18 | a0001c0001t0003g0007a0001c0001t0003g0288a0001c0001t0004g0157others(15): Show | 18 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+21156A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139101 | ||||||
| chr6:116139177
|
T | C | 14 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0003g0049others(11): Show | 14 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+21232T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139177 | ||||||
| chr6:116139256
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21311A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139256 | ||||||
| chr6:116139493
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21548A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139493 | ||||||
| chr6:116139571
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+21626A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139571 | ||||||
| chr6:116139657
|
T | C | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+21712T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139657 | ||||||
| chr6:116139670
|
A | G | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+21725A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139670 | ||||||
| chr6:116139926
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+21981G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116139926 | ||||||
| chr6:116140032
|
T | C | 1 | a0001c0001t0039g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.529+22087T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140032 | ||||||
| chr6:116140241
|
C | A | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+22296C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140241 | ||||||
| chr6:116140314
|
T | C | 178 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0047others(175): Show | 182 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.529+22369T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140314 | ||||||
| chr6:116140335
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.529+22390C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140335 | ||||||
| chr6:116140393
|
C | T | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+22448C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140393 | ||||||
| chr6:116140398
|
A | G | 1 | a0001c0003t0014g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+22453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140398 | ||||||
| chr6:116140451
|
G | A | 67 | a0001c0001t0001g0043a0001c0001t0002g0098a0001c0001t0003g0002others(64): Show | 69 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.529+22506G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140451 | ||||||
| chr6:116140465
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+22520A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140465 | ||||||
| chr6:116140475
|
C | T | 17 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0068others(14): Show | 17 | HG00642.hp1 HG00738.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.529+22530C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140475 | ||||||
| chr6:116140812
|
G | A | 1 | a0001c0001t0003g0046 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.529+22867G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140812 | ||||||
| chr6:116140920
|
A | C | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+22975A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140920 | ||||||
| chr6:116140947
|
T | C | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.529+23002T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140947 | ||||||
| chr6:116140995
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+23050A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116140995 | ||||||
| chr6:116141112
|
C | T | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+23167C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141112 | ||||||
| chr6:116141263
|
A | AT | 14 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241others(11): Show | 14 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+23330dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141263 | |||||
| chr6:116141397
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.529+23452T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141397 | ||||||
| chr6:116141489
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23544T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141489 | ||||||
| chr6:116141601
|
A | G | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+23656A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141601 | ||||||
| chr6:116141629
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23684T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141629 | ||||||
| chr6:116141759
|
G | GT | 10 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG00099.hp2 HG01891.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+23826dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141759 | |||||
| chr6:116141786
|
C | T | 1 | a0001c0001t0005g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.529+23841C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141786 | ||||||
| chr6:116141798
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+23853T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141798 | ||||||
| chr6:116141849
|
GTC | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+23906_529+2390 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141849 | |||||
| chr6:116141885
|
A | AAC | 44 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0125others(41): Show | 45 | HG00280.hp1 HG00738.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.529+23981_529+2398 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACAC | 21 | a0001c0001t0001g0121a0001c0001t0001g0148a0001c0001t0001g0186others(18): Show | 21 | HG00642.hp1 HG00642.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.529+23979_529+2398 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACAC | 14 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+23977_529+2398 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACACA others(1): Show |
8 | a0001c0001t0001g0126a0001c0001t0002g0279a0001c0001t0003g0291others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+23975_529+2398 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACACA others(7): Show |
1 | a0001c0001t0009g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.529+23969_529+2398 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACACA others(9): Show |
4 | a0001c0001t0003g0112a0001c0001t0009g0278a0001c0001t0009g0290others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+23967_529+2398 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACACA others(11): Show |
5 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0009g0107others(2): Show | 5 | HG02630.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+23965_529+2398 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
A | AACACACA others(13): Show |
1 | a0001c0001t0009g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.529+23963_529+2398 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
AAC | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0136a0001c0001t0001g0180others(4): Show | 7 | HG01074.hp2 HG02071.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+23981_529+2398 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
AACAC | A | 28 | a0001c0001t0001g0200a0001c0001t0002g0074a0001c0001t0002g0240others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.529+23979_529+2398 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141885
|
AACACAC | A | 63 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0193others(60): Show | 65 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.529+23977_529+2398 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116141885 | |||||
| chr6:116141915
|
C | A | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+23970C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141915 | ||||||
| chr6:116141926
|
A | T | 1 | a0001c0001t0001g0208 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.529+23981A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116141926 | ||||||
| chr6:116142059
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0024g0122 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.529+24114T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142059 | ||||||
| chr6:116142085
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.529+24140A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142085 | ||||||
| chr6:116142155
|
T | A | 117 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0054others(114): Show | 119 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.529+24210T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142155 | ||||||
| chr6:116142179
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.529+24234T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142179 | ||||||
| chr6:116142238
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+24293G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142238 | ||||||
| chr6:116142284
|
C | CT | 8 | a0001c0001t0002g0098a0001c0001t0005g0095a0001c0001t0005g0097others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+24348dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116142284 | |||||
| chr6:116142589
|
CTG | C | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+24648_529+2464 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116142589 | |||||
| chr6:116142724
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+24779T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142724 | ||||||
| chr6:116142931
|
A | C | 17 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(14): Show | 18 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+24986A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142931 | ||||||
| chr6:116142985
|
A | G | 1 | a0001c0001t0004g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.529+25040A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116142985 | ||||||
| chr6:116143056
|
A | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+25111A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143056 | ||||||
| chr6:116143069
|
C | T | 91 | a0001c0001t0001g0043a0001c0001t0002g0053a0001c0001t0002g0098others(88): Show | 93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+25124C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143069 | ||||||
| chr6:116143100
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+25155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143100 | ||||||
| chr6:116143113
|
G | A | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.529+25168G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143113 | ||||||
| chr6:116143250
|
C | T | 6 | a0001c0001t0003g0013a0001c0001t0003g0028a0001c0001t0003g0039others(3): Show | 6 | HG02055.hp2 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+25305C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143250 | ||||||
| chr6:116143337
|
A | G | 1 | a0001c0001t0003g0023 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.529+25392A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143337 | ||||||
| chr6:116143405
|
T | C | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+25460T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143405 | ||||||
| chr6:116143406
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+25461G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143406 | ||||||
| chr6:116143507
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.529+25562C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143507 | ||||||
| chr6:116143667
|
T | C | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+25722T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116143667 | ||||||
| chr6:116144177
|
A | G | 1 | a0001c0001t0005g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.529+26232A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144177 | ||||||
| chr6:116144241
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.529+26296C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144241 | ||||||
| chr6:116144257
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.529+26312C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144257 | ||||||
| chr6:116144271
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26326G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144271 | ||||||
| chr6:116144277
|
C | T | 1 | a0001c0001t0007g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.529+26332C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144277 | ||||||
| chr6:116144280
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26335A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144280 | ||||||
| chr6:116144366
|
T | C | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+26421T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144366 | ||||||
| chr6:116144451
|
ATGT | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(58): Show | 63 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.529+26510_529+2651 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144451 | |||||
| chr6:116144466
|
A | G | 3 | a0001c0001t0007g0130a0001c0001t0007g0131a0001c0001t0007g0132 | 3 | HG02559.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.529+26521A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144466 | ||||||
| chr6:116144489
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+26544G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144489 | ||||||
| chr6:116144495
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+26550G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144495 | ||||||
| chr6:116144499
|
C | CA | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02809.hp2 NA18947.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+26568dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144499 | |||||
| chr6:116144499
|
CA | C | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.529+26568delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116144499 | |||||
| chr6:116144512
|
A | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+26567A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144512 | ||||||
| chr6:116144525
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.529+26580G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144525 | ||||||
| chr6:116144575
|
T | C | 1 | a0001c0001t0006g0052 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.529+26630T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144575 | ||||||
| chr6:116144648
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+26703G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144648 | ||||||
| chr6:116144807
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+26862G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144807 | ||||||
| chr6:116144914
|
G | A | 8 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+26969G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116144914 | ||||||
| chr6:116145021
|
T | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+27076T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145021 | ||||||
| chr6:116145064
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27119T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145064 | ||||||
| chr6:116145066
|
T | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0156a0001c0001t0001g0159others(11): Show | 16 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(13): Show |
intron_variant | MODIFIER | c.529+27121T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145066 | ||||||
| chr6:116145091
|
T | C | 8 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+27146T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145091 | ||||||
| chr6:116145194
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+27249C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145194 | ||||||
| chr6:116145217
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27272A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145217 | ||||||
| chr6:116145506
|
G | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+27561G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145506 | ||||||
| chr6:116145681
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+27736C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145681 | ||||||
| chr6:116145827
|
G | A | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+27882G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145827 | ||||||
| chr6:116145941
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+27996A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145941 | ||||||
| chr6:116145948
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529+28003C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116145948 | ||||||
| chr6:116146013
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28068C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146013 | ||||||
| chr6:116146133
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28188A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146133 | ||||||
| chr6:116146211
|
G | A | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+28266G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146211 | ||||||
| chr6:116146262
|
C | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28317C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146262 | ||||||
| chr6:116146543
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.529+28598T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146543 | ||||||
| chr6:116146565
|
A | C | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+28620A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146565 | ||||||
| chr6:116146608
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+28663A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146608 | ||||||
| chr6:116146726
|
C | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529+28781C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146726 | ||||||
| chr6:116146817
|
T | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+28872T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146817 | ||||||
| chr6:116146827
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+28882A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116146827 | ||||||
| chr6:116147000
|
A | AAT | 177 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0047others(174): Show | 181 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.529+29068_529+2906 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116147000 | |||||
| chr6:116147049
|
G | A | 4 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0007g0246others(1): Show | 4 | HG02818.hp1 HG03225.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+29104G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147049 | ||||||
| chr6:116147113
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+29168A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147113 | ||||||
| chr6:116147152
|
A | T | 35 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(32): Show | 36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+29207A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147152 | ||||||
| chr6:116147247
|
G | A | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.529+29302G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147247 | ||||||
| chr6:116147336
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+29391G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147336 | ||||||
| chr6:116147456
|
A | T | 2 | a0001c0001t0003g0007a0001c0001t0008g0008 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+29511A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147456 | ||||||
| chr6:116147495
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.529+29550A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147495 | ||||||
| chr6:116147815
|
G | A | 7 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+29870G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147815 | ||||||
| chr6:116147850
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+29905G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147850 | ||||||
| chr6:116147941
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529+29996G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147941 | ||||||
| chr6:116147984
|
C | CA | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30051dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116147984 | |||||
| chr6:116147999
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+30054T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116147999 | ||||||
| chr6:116148000
|
G | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+30055G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148000 | ||||||
| chr6:116148046
|
G | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.529+30101G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148046 | ||||||
| chr6:116148089
|
G | A | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+30144G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148089 | ||||||
| chr6:116148146
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+30201A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148146 | ||||||
| chr6:116148213
|
T | G | 2 | a0001c0001t0003g0007a0001c0001t0008g0008 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+30268T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148213 | ||||||
| chr6:116148252
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(55): Show | 60 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.529+30307A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148252 | ||||||
| chr6:116148288
|
T | C | 14 | a0001c0001t0002g0053a0001c0001t0002g0263a0001c0001t0002g0264others(11): Show | 14 | HG01515.hp1 HG01934.hp1 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+30343T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148288 | ||||||
| chr6:116148338
|
A | C | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+30393A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148338 | ||||||
| chr6:116148421
|
A | G | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+30476A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148421 | ||||||
| chr6:116148429
|
A | G | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30484A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148429 | ||||||
| chr6:116148540
|
T | C | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+30595T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148540 | ||||||
| chr6:116148583
|
A | G | 1 | a0001c0001t0008g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+30638A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148583 | ||||||
| chr6:116148594
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+30649T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148594 | ||||||
| chr6:116148740
|
C | T | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+30795C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116148740 | ||||||
| chr6:116149288
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.529+31343A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149288 | ||||||
| chr6:116149398
|
A | G | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+31453A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149398 | ||||||
| chr6:116149462
|
A | G | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+31517A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149462 | ||||||
| chr6:116149604
|
T | G | 16 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(13): Show | 16 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.529+31659T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149604 | ||||||
| chr6:116149723
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+31778T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149723 | ||||||
| chr6:116149880
|
C | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(2): Show | 5 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+31935C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149880 | ||||||
| chr6:116149894
|
G | A | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+31949G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149894 | ||||||
| chr6:116149909
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+31964G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149909 | ||||||
| chr6:116149915
|
T | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+31970T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116149915 | ||||||
| chr6:116150207
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32262T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150207 | ||||||
| chr6:116150233
|
C | T | 1 | a0001c0001t0011g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.529+32288C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150233 | ||||||
| chr6:116150247
|
C | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32302C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150247 | ||||||
| chr6:116150266
|
G | GT | 18 | a0001c0001t0001g0138a0001c0001t0001g0154a0001c0001t0001g0209others(15): Show | 18 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+32331dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116150266 | |||||
| chr6:116150434
|
G | A | 1 | a0001c0001t0003g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.529+32489G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150434 | ||||||
| chr6:116150537
|
G | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+32592G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150537 | ||||||
| chr6:116150595
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+32650G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150595 | ||||||
| chr6:116150636
|
G | A | 2 | a0001c0001t0019g0149a0001c0001t0019g0150 | 2 | HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.529+32691G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150636 | ||||||
| chr6:116150656
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+32711A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150656 | ||||||
| chr6:116150761
|
G | A | 2 | a0001c0001t0002g0240a0001c0001t0002g0245 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.529+32816G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116150761 | ||||||
| chr6:116151071
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.529+33126T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151071 | ||||||
| chr6:116151079
|
TGAATTTG others(11): Show |
T | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+33143_529+3316 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116151079 | |||||
| chr6:116151082
|
A | G | 1 | a0001c0001t0005g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+33137A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151082 | ||||||
| chr6:116151105
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.529+33160C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151105 | ||||||
| chr6:116151154
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33209C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151154 | ||||||
| chr6:116151416
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33471C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151416 | ||||||
| chr6:116151449
|
A | G | 3 | a0001c0001t0016g0116a0001c0001t0016g0117a0001c0001t0025g0115 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+33504A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151449 | ||||||
| chr6:116151542
|
C | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+33597C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151542 | ||||||
| chr6:116151594
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33649A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151594 | ||||||
| chr6:116151605
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+33660G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151605 | ||||||
| chr6:116151746
|
A | C | 69 | a0001c0001t0001g0043a0001c0001t0002g0098a0001c0001t0003g0002others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.529+33801A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116151746 | ||||||
| chr6:116152025
|
A | T | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+34080A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152025 | ||||||
| chr6:116152104
|
G | T | 19 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(16): Show | 19 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+34159G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152104 | ||||||
| chr6:116152130
|
C | A | 4 | a0001c0001t0003g0002a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 5 | NA18947.hp1 NA18957.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+34185C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152130 | ||||||
| chr6:116152371
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+34426G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152371 | ||||||
| chr6:116152483
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.529+34538A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152483 | ||||||
| chr6:116152616
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+34671C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152616 | ||||||
| chr6:116152694
|
T | C | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+34749T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152694 | ||||||
| chr6:116152776
|
C | A | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+34831C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152776 | ||||||
| chr6:116152781
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+34836C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116152781 | ||||||
| chr6:116153323
|
A | G | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+35378A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153323 | ||||||
| chr6:116153340
|
GTT | G | 153 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(150): Show | 157 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.529+35399_529+3540 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116153340 | |||||
| chr6:116153366
|
A | G | 4 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+35421A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153366 | ||||||
| chr6:116153421
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.529+35476T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153421 | ||||||
| chr6:116153624
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529+35679G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153624 | ||||||
| chr6:116153648
|
A | G | 1 | a0001c0001t0004g0255 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.529+35703A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153648 | ||||||
| chr6:116153737
|
T | C | 22 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(19): Show | 22 | HG01515.hp1 HG01934.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+35792T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153737 | ||||||
| chr6:116153874
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529+35929G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153874 | ||||||
| chr6:116153913
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+35968G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116153913 | ||||||
| chr6:116154029
|
CT | C | 29 | a0001c0001t0001g0176a0001c0001t0001g0186a0001c0001t0001g0221others(26): Show | 29 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.529+36102delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116154029 | |||||
| chr6:116154085
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36140A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154085 | ||||||
| chr6:116154088
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.529+36143A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154088 | ||||||
| chr6:116154129
|
G | A | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.529+36184G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154129 | ||||||
| chr6:116154169
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+36224A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154169 | ||||||
| chr6:116154325
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.529+36380G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154325 | ||||||
| chr6:116154327
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.529+36382G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154327 | ||||||
| chr6:116154359
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36414C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154359 | ||||||
| chr6:116154394
|
T | G | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+36449T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154394 | ||||||
| chr6:116154431
|
G | C | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+36486G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154431 | ||||||
| chr6:116154658
|
AT | A | 38 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(35): Show | 40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+36715delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116154658 | |||||
| chr6:116154751
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+36806A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154751 | ||||||
| chr6:116154904
|
A | G | 8 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+36959A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116154904 | ||||||
| chr6:116155093
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.529+37148C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155093 | ||||||
| chr6:116155182
|
C | G | 7 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.529+37237C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155182 | ||||||
| chr6:116155246
|
TTA | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0283a0001c0001t0023g0123 | 3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+37306_529+3730 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155246 | |||||
| chr6:116155251
|
T | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0283a0001c0001t0023g0123 | 3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+37306T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155251 | ||||||
| chr6:116155409
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529+37464A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155409 | ||||||
| chr6:116155410
|
T | C | 2 | a0001c0001t0003g0291a0001c0001t0006g0118 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+37465T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155410 | ||||||
| chr6:116155437
|
G | A | 19 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(16): Show | 19 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.529+37492G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155437 | ||||||
| chr6:116155516
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37571G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155516 | ||||||
| chr6:116155541
|
C | T | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+37596C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155541 | ||||||
| chr6:116155605
|
G | A | 1 | a0003c0004t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.529+37660G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155605 | ||||||
| chr6:116155709
|
T | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+37764T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155709 | ||||||
| chr6:116155721
|
C | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | NA18942.hp1 NA19065.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.529+37776C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155721 | ||||||
| chr6:116155752
|
T | TA | 9 | a0001c0001t0001g0094a0001c0001t0001g0201a0001c0001t0003g0018others(6): Show | 9 | HG01346.hp2 HG02280.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37827dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155752 | |||||
| chr6:116155752
|
TA | T | 46 | a0001c0001t0001g0075a0001c0001t0001g0145a0001c0001t0001g0146others(43): Show | 46 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.529+37827delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116155752 | |||||
| chr6:116155776
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+37831G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155776 | ||||||
| chr6:116155844
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529+37899G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116155844 | ||||||
| chr6:116156115
|
C | T | 155 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(152): Show | 159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.529+38170C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156115 | ||||||
| chr6:116156330
|
A | C | 21 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(18): Show | 22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+38385A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156330 | ||||||
| chr6:116156334
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.529+38389C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156334 | ||||||
| chr6:116156355
|
C | T | 153 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(150): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.529+38410C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156355 | ||||||
| chr6:116156457
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.529+38512C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156457 | ||||||
| chr6:116156547
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.529+38602G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156547 | ||||||
| chr6:116156753
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0221 | 2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.529+38808C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156753 | ||||||
| chr6:116156826
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.529+38881C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156826 | ||||||
| chr6:116156890
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.529+38945T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156890 | ||||||
| chr6:116156936
|
C | A | 2 | a0001c0001t0002g0269a0001c0001t0002g0274 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.529+38991C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156936 | ||||||
| chr6:116156937
|
A | G | 2 | a0001c0001t0002g0269a0001c0001t0002g0274 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.529+38992A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116156937 | ||||||
| chr6:116157024
|
C | T | 154 | a0001c0001t0001g0043a0001c0001t0002g0004a0001c0001t0002g0053others(151): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.529+39079C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157024 | ||||||
| chr6:116157150
|
T | C | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+39205T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157150 | ||||||
| chr6:116157315
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+39370C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157315 | ||||||
| chr6:116157341
|
C | T | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529+39396C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157341 | ||||||
| chr6:116157367
|
A | G | 1 | a0001c0001t0008g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+39422A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157367 | ||||||
| chr6:116157558
|
G | A | 2 | a0001c0001t0007g0246a0001c0001t0035g0292 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529+39613G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157558 | ||||||
| chr6:116157718
|
A | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0026 | 2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.529+39773A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157718 | ||||||
| chr6:116157779
|
C | T | 1 | a0001c0001t0007g0271 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.529+39834C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157779 | ||||||
| chr6:116157788
|
C | G | 93 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0053others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.529+39843C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116157788 | ||||||
| chr6:116158008
|
G | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+40063G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158008 | ||||||
| chr6:116158086
|
C | G | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.529+40141C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158086 | ||||||
| chr6:116158138
|
A | C | 1 | a0001c0001t0002g0082 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.529+40193A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158138 | ||||||
| chr6:116158219
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.529+40274A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158219 | ||||||
| chr6:116158618
|
A | G | 1 | a0001c0001t0005g0134 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.529+40673A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158618 | ||||||
| chr6:116158793
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+40848T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158793 | ||||||
| chr6:116158834
|
G | A | 2 | a0001c0001t0032g0243a0001c0001t0033g0281 | 2 | HG01074.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.529+40889G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116158834 | ||||||
| chr6:116159145
|
C | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0188a0001c0001t0001g0197others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.529+41200C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159145 | ||||||
| chr6:116159154
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+41209A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159154 | ||||||
| chr6:116159295
|
A | G | 182 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(179): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.529+41350A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159295 | ||||||
| chr6:116159456
|
C | T | 2 | a0001c0001t0015g0284a0001c0001t0015g0289 | 2 | HG00738.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.529+41511C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159456 | ||||||
| chr6:116159574
|
G | A | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+41629G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159574 | ||||||
| chr6:116159724
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.529+41779A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159724 | ||||||
| chr6:116159782
|
C | T | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+41837C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159782 | ||||||
| chr6:116159870
|
T | C | 11 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(8): Show | 11 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+41925T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159870 | ||||||
| chr6:116159909
|
T | G | 1 | a0001c0001t0005g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.529+41964T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116159909 | ||||||
| chr6:116160107
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42162T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160107 | ||||||
| chr6:116160371
|
T | A | 1 | a0001c0001t0015g0289 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.529+42426T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160371 | ||||||
| chr6:116160437
|
TC | T | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.529+42494delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116160437 | |||||
| chr6:116160467
|
G | A | 4 | a0001c0001t0011g0090a0001c0001t0011g0091a0001c0001t0011g0213others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+42522G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160467 | ||||||
| chr6:116160526
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42581C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160526 | ||||||
| chr6:116160576
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+42631A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160576 | ||||||
| chr6:116160701
|
G | T | 1 | a0001c0001t0003g0046 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.529+42756G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160701 | ||||||
| chr6:116160779
|
T | A | 2 | a0001c0001t0009g0110a0001c0001t0030g0113 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.529+42834T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160779 | ||||||
| chr6:116160780
|
A | T | 2 | a0001c0001t0009g0110a0001c0001t0030g0113 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.529+42835A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160780 | ||||||
| chr6:116160907
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42962T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160907 | ||||||
| chr6:116160936
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0260 | 2 | HG02074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.529+42991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160936 | ||||||
| chr6:116160943
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+42998G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116160943 | ||||||
| chr6:116161152
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+43207G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161152 | ||||||
| chr6:116161198
|
G | A | 2 | a0001c0001t0003g0007a0001c0001t0008g0008 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.529+43253G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161198 | ||||||
| chr6:116161260
|
A | G | 1 | a0001c0001t0036g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.529+43315A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161260 | ||||||
| chr6:116161395
|
A | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0279others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+43450A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161395 | ||||||
| chr6:116161724
|
C | T | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+43779C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161724 | ||||||
| chr6:116161770
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+43825A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161770 | ||||||
| chr6:116161775
|
TAATTTGA others(7): Show |
T | 3 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212 | 3 | HG02074.hp2 HG02132.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.529+43831_529+4384 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161775 | ||||||
| chr6:116161784
|
G | A | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+43839G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161784 | ||||||
| chr6:116161851
|
T | C | 35 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(32): Show | 36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+43906T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161851 | ||||||
| chr6:116161894
|
A | G | 1 | a0001c0001t0012g0169 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.529+43949A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116161894 | ||||||
| chr6:116161979
|
TA | T | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0002c0002t0002g0069others(1): Show | 4 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+44037delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116161979 | |||||
| chr6:116162355
|
A | T | 1 | a0001c0001t0004g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.529+44410A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162355 | ||||||
| chr6:116162443
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.529+44498A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162443 | ||||||
| chr6:116162523
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.529+44578T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162523 | ||||||
| chr6:116162641
|
A | T | 20 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(17): Show | 20 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.529+44696A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162641 | ||||||
| chr6:116162847
|
G | A | 94 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.529+44902G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162847 | ||||||
| chr6:116162943
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0136 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.529+44998T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162943 | ||||||
| chr6:116162955
|
G | A | 1 | a0001c0001t0015g0289 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.529+45010G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116162955 | ||||||
| chr6:116163075
|
C | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45130C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163075 | ||||||
| chr6:116163082
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45137G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163082 | ||||||
| chr6:116163106
|
G | A | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+45161G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163106 | ||||||
| chr6:116163126
|
C | CAAAAA | 11 | a0001c0001t0002g0098a0001c0001t0003g0044a0001c0001t0003g0233others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+45193_529+4519 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | |||||
| chr6:116163126
|
C | CAAAAAA | 66 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0051others(63): Show | 68 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.529+45192_529+4519 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | |||||
| chr6:116163126
|
C | CAAAAAAA | 9 | a0001c0001t0002g0085a0001c0001t0003g0012a0001c0001t0003g0018others(6): Show | 9 | HG01346.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+45191_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163126 | |||||
| chr6:116163135
|
A | AATAT | 29 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(26): Show | 31 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.529+45191_529+4519 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | |||||
| chr6:116163135
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0159 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.529+45191_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | |||||
| chr6:116163135
|
A | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0210 | 2 | HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.529+45190A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163135 | ||||||
| chr6:116163135
|
AAAAAAAA others(9): Show |
A | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+45192_529+4520 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163135 | |||||
| chr6:116163137
|
A | AATAT | 10 | a0001c0001t0001g0094a0001c0001t0001g0188a0001c0001t0001g0200others(7): Show | 10 | HG00323.hp1 HG02300.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+45193_529+4519 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163137 | |||||
| chr6:116163137
|
A | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(42): Show | 47 | HG00408.hp1 HG00558.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.529+45192A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163137 | ||||||
| chr6:116163139
|
A | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0075others(83): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.529+45194A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163139 | ||||||
| chr6:116163141
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(21): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0009g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAAAA others(4): Show |
12 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(9): Show | 12 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0009g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAAAT | 17 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(14): Show | 18 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0279 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAATA others(23): Show |
1 | a0001c0001t0002g0293 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(34): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAATA others(39): Show |
1 | a0001c0001t0017g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(50): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAAT | 7 | a0001c0001t0002g0053a0001c0001t0002g0239a0001c0001t0002g0240others(4): Show | 7 | HG01515.hp1 HG01934.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAATAT | 9 | a0001c0001t0002g0047a0001c0001t0002g0263a0001c0001t0002g0264others(6): Show | 9 | HG01099.hp2 NA18953.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+45197_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0002g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0037g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAATATA others(13): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.529+45197_529+4519 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAAATATA others(19): Show |
1 | a0001c0001t0017g0294 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.529+45197_529+4519 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057 | 3 | HG01884.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.529+45197_529+4519 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0002g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.529+45197_529+4519 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AATATATA others(3): Show |
1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45209_529+4521 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AATATATA others(11): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+45201_529+4521 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AATATATA others(13): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0023g0123 | 3 | HG01891.hp2 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.529+45199_529+4521 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529+45197_529+4521 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116163141 | |||||
| chr6:116163141
|
A | ATATATAT | 5 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0007g0131others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+45196_529+4519 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | ||||||
| chr6:116163141
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0024g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.529+45196_529+4519 others(23): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | ||||||
| chr6:116163141
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0075others(88): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.529+45196A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163141 | ||||||
| chr6:116163143
|
T | A | 63 | a0001c0001t0002g0098a0001c0001t0003g0002a0001c0001t0003g0003others(60): Show | 65 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.529+45198T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163143 | ||||||
| chr6:116163145
|
T | A | 6 | a0001c0001t0003g0014a0001c0001t0003g0041a0001c0001t0003g0233others(3): Show | 6 | HG01884.hp1 HG02132.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+45200T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163145 | ||||||
| chr6:116163147
|
T | A | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.529+45202T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163147 | ||||||
| chr6:116163197
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.529+45252A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163197 | ||||||
| chr6:116163240
|
T | G | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529+45295T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163240 | ||||||
| chr6:116163290
|
A | G | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45345A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163290 | ||||||
| chr6:116163354
|
G | T | 2 | a0002c0002t0002g0069a0002c0002t0002g0081 | 2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.529+45409G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163354 | ||||||
| chr6:116163437
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+45492T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163437 | ||||||
| chr6:116163546
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+45601T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163546 | ||||||
| chr6:116163714
|
G | A | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+45769G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163714 | ||||||
| chr6:116163905
|
T | C | 11 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(8): Show | 11 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+45960T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163905 | ||||||
| chr6:116163957
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46012G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163957 | ||||||
| chr6:116163957
|
G | C | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+46012G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116163957 | ||||||
| chr6:116164256
|
T | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46311T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164256 | ||||||
| chr6:116164325
|
T | G | 1 | a0001c0001t0005g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.529+46380T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164325 | ||||||
| chr6:116164438
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+46493A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164438 | ||||||
| chr6:116164471
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.529+46526G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164471 | ||||||
| chr6:116164559
|
C | T | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+46614C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164559 | ||||||
| chr6:116164732
|
T | G | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104 | 3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.529+46787T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164732 | ||||||
| chr6:116164834
|
C | A | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529+46889C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164834 | ||||||
| chr6:116164927
|
T | A | 2 | a0001c0001t0009g0278a0001c0001t0009g0290 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.529+46982T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164927 | ||||||
| chr6:116164935
|
T | A | 1 | a0001c0001t0001g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.529+46990T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164935 | ||||||
| chr6:116164939
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.529+46994A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164939 | ||||||
| chr6:116164989
|
C | T | 38 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(35): Show | 40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.529+47044C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116164989 | ||||||
| chr6:116165061
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.529+47116C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165061 | ||||||
| chr6:116165075
|
C | T | 2 | a0001c0001t0006g0005a0001c0001t0014g0247 | 3 | HG02809.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+47130C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165075 | ||||||
| chr6:116165098
|
G | GAA | 21 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(18): Show | 21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.529+47172_529+4717 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAA | 81 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0066others(78): Show | 84 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.529+47171_529+4717 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAAA | 35 | a0001c0001t0002g0004a0001c0001t0002g0054a0001c0001t0002g0055others(32): Show | 36 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.529+47170_529+4717 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAAAA | 18 | a0001c0001t0002g0068a0001c0001t0002g0082a0001c0001t0002g0083others(15): Show | 18 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+47169_529+4717 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAAAAA | 11 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+47168_529+4717 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAAAAAA | 18 | a0001c0001t0001g0283a0001c0001t0001g0285a0001c0001t0001g0287others(15): Show | 18 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.529+47167_529+4717 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
G | GAAAAAAA others(1): Show |
9 | a0001c0001t0001g0286a0001c0001t0002g0051a0001c0001t0006g0009others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+47166_529+4717 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165098
|
GA | G | 6 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01168.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+47173delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116165098 | |||||
| chr6:116165121
|
A | C | 110 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(107): Show | 112 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.529+47176A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165121 | ||||||
| chr6:116165265
|
G | C | 1 | a0001c0001t0003g0038 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.529+47320G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165265 | ||||||
| chr6:116165293
|
A | G | 8 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.529+47348A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165293 | ||||||
| chr6:116165297
|
T | A | 94 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.529+47352T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165297 | ||||||
| chr6:116165342
|
C | T | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529+47397C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165342 | ||||||
| chr6:116165425
|
G | A | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+47480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165425 | ||||||
| chr6:116165481
|
G | T | 3 | a0001c0001t0003g0049a0001c0001t0004g0050a0001c0001t0029g0048 | 3 | HG01106.hp2 NA20905.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.529+47536G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165481 | ||||||
| chr6:116165584
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+47639C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165584 | ||||||
| chr6:116165629
|
C | A | 69 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.529+47684C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165629 | ||||||
| chr6:116165654
|
G | C | 9 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+47709G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165654 | ||||||
| chr6:116165797
|
G | T | 2 | a0001c0001t0015g0284a0001c0001t0015g0289 | 2 | HG00738.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.529+47852G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165797 | ||||||
| chr6:116165996
|
C | G | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+48051C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116165996 | ||||||
| chr6:116166052
|
T | C | 4 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0007g0131others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+48107T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166052 | ||||||
| chr6:116166053
|
A | G | 2 | a0001c0001t0003g0291a0001c0001t0006g0118 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+48108A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166053 | ||||||
| chr6:116166177
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+48232C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166177 | ||||||
| chr6:116166419
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+48474A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166419 | ||||||
| chr6:116166880
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.529+48935G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116166880 | ||||||
| chr6:116167093
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+49148G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167093 | ||||||
| chr6:116167206
|
A | AT | 64 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0154others(61): Show | 65 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.529+49286dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | |||||
| chr6:116167206
|
A | ATT | 24 | a0001c0001t0001g0178a0001c0001t0002g0066a0001c0001t0002g0068others(21): Show | 24 | HG00639.hp1 HG01069.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.529+49285_529+4928 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | |||||
| chr6:116167206
|
AT | A | 56 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0125others(53): Show | 56 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.529+49286delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116167206 | |||||
| chr6:116167252
|
C | T | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.529+49307C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167252 | ||||||
| chr6:116167374
|
G | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+49429G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167374 | ||||||
| chr6:116167403
|
A | G | 1 | a0001c0001t0006g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.529+49458A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167403 | ||||||
| chr6:116167414
|
G | A | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+49469G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167414 | ||||||
| chr6:116167445
|
C | T | 10 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.529+49500C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167445 | ||||||
| chr6:116167503
|
T | C | 2 | a0001c0001t0004g0157a0001c0001t0004g0183 | 2 | NA18991.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.529+49558T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167503 | ||||||
| chr6:116167551
|
G | T | 3 | a0001c0001t0016g0116a0001c0001t0016g0117a0001c0001t0025g0115 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529+49606G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167551 | ||||||
| chr6:116167581
|
A | G | 1 | a0001c0001t0008g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.529+49636A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167581 | ||||||
| chr6:116167646
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.529+49701C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167646 | ||||||
| chr6:116167692
|
C | T | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529+49747C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167692 | ||||||
| chr6:116167740
|
A | G | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.529+49795A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167740 | ||||||
| chr6:116167743
|
A | G | 182 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(179): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.529+49798A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167743 | ||||||
| chr6:116167762
|
G | A | 21 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(18): Show | 22 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.529+49817G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167762 | ||||||
| chr6:116167762
|
G | C | 2 | a0001c0001t0009g0278a0001c0001t0009g0290 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.529+49817G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167762 | ||||||
| chr6:116167848
|
G | C | 1 | a0001c0001t0006g0005 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+49903G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167848 | ||||||
| chr6:116167854
|
G | A | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.529+49909G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116167854 | ||||||
| chr6:116168083
|
CT | C | 76 | a0001c0001t0001g0011a0001c0001t0001g0168a0001c0001t0001g0192others(73): Show | 78 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.529+50157delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116168083 | |||||
| chr6:116168103
|
A | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+50158A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168103 | ||||||
| chr6:116168175
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+50230A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168175 | ||||||
| chr6:116168314
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+50369T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168314 | ||||||
| chr6:116168387
|
A | G | 24 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.529+50442A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168387 | ||||||
| chr6:116168450
|
A | G | 1 | a0001c0001t0037g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.529+50505A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168450 | ||||||
| chr6:116168628
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.529+50683A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168628 | ||||||
| chr6:116168691
|
T | C | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529+50746T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168691 | ||||||
| chr6:116168812
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.529+50867T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168812 | ||||||
| chr6:116168812
|
T | G | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+50867T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116168812 | ||||||
| chr6:116169006
|
T | C | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0279others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+51061T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169006 | ||||||
| chr6:116169163
|
C | CT | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+51219dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116169163 | |||||
| chr6:116169173
|
CT | C | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+51232delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116169173 | |||||
| chr6:116169376
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | NA18940.hp1 NA19004.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+51431T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169376 | ||||||
| chr6:116169396
|
C | G | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.529+51451C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169396 | ||||||
| chr6:116169539
|
G | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-51515G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169539 | ||||||
| chr6:116169566
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0019g0149a0001c0001t0019g0150 | 3 | HG01099.hp2 HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.530-51488C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169566 | ||||||
| chr6:116169660
|
T | G | 3 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023 | 3 | NA18947.hp1 NA19088.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.530-51394T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169660 | ||||||
| chr6:116169675
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-51379A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169675 | ||||||
| chr6:116169715
|
T | A | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.530-51339T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169715 | ||||||
| chr6:116169727
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.530-51327A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169727 | ||||||
| chr6:116169799
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-51255C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116169799 | ||||||
| chr6:116170139
|
G | A | 65 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(62): Show | 67 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.530-50915G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170139 | ||||||
| chr6:116170169
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.530-50885G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170169 | ||||||
| chr6:116170170
|
G | A | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-50884G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170170 | ||||||
| chr6:116170245
|
TC | T | 35 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(32): Show | 36 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.530-50805delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116170245 | |||||
| chr6:116170292
|
G | T | 16 | a0001c0001t0003g0007a0001c0001t0003g0288a0001c0001t0004g0157others(13): Show | 16 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.530-50762G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170292 | ||||||
| chr6:116170559
|
G | T | 1 | a0001c0001t0004g0254 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.530-50495G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170559 | ||||||
| chr6:116170693
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-50361G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170693 | ||||||
| chr6:116170838
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-50216C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116170838 | ||||||
| chr6:116171014
|
C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-50040C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171014 | ||||||
| chr6:116171062
|
G | A | 2 | a0001c0001t0002g0293a0001c0001t0017g0059 | 2 | HG01981.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.530-49992G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171062 | ||||||
| chr6:116171187
|
T | C | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-49867T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171187 | ||||||
| chr6:116171269
|
C | T | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-49785C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171269 | ||||||
| chr6:116171336
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-49718G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171336 | ||||||
| chr6:116171337
|
T | C | 94 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-49717T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171337 | ||||||
| chr6:116171395
|
A | G | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-49659A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171395 | ||||||
| chr6:116171553
|
A | G | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-49501A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171553 | ||||||
| chr6:116171561
|
G | A | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-49493G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171561 | ||||||
| chr6:116171562
|
G | T | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-49492G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171562 | ||||||
| chr6:116171695
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-49359G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116171695 | ||||||
| chr6:116172067
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-48987A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172067 | ||||||
| chr6:116172183
|
A | C | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-48871A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172183 | ||||||
| chr6:116172317
|
C | CT | 128 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0126others(125): Show | 131 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.530-48715dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | |||||
| chr6:116172317
|
C | CTT | 10 | a0001c0001t0002g0241a0001c0001t0003g0019a0001c0001t0003g0023others(7): Show | 10 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-48716_530-4871 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | |||||
| chr6:116172317
|
CT | C | 13 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0063others(10): Show | 13 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.530-48715delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | |||||
| chr6:116172317
|
CTT | C | 14 | a0001c0001t0002g0055a0001c0001t0002g0106a0001c0001t0002g0111others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-48716_530-4871 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116172317 | |||||
| chr6:116172367
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.530-48687G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172367 | ||||||
| chr6:116172396
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-48658G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172396 | ||||||
| chr6:116172611
|
C | T | 4 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262others(1): Show | 4 | HG02717.hp2 HG03239.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-48443C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172611 | ||||||
| chr6:116172646
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-48408A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116172646 | ||||||
| chr6:116173201
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-47853A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173201 | ||||||
| chr6:116173387
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.530-47667G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173387 | ||||||
| chr6:116173400
|
G | A | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-47654G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173400 | ||||||
| chr6:116173465
|
G | T | 1 | a0001c0001t0003g0191 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.530-47589G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173465 | ||||||
| chr6:116173674
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-47380T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173674 | ||||||
| chr6:116173777
|
A | G | 190 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0001g0160others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-47277A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116173777 | ||||||
| chr6:116174174
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-46880A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174174 | ||||||
| chr6:116174280
|
C | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.530-46774C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174280 | ||||||
| chr6:116174341
|
C | T | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-46713C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174341 | ||||||
| chr6:116174442
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-46612A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174442 | ||||||
| chr6:116174554
|
G | T | 138 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(135): Show | 142 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.530-46500G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174554 | ||||||
| chr6:116174706
|
C | G | 8 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(5): Show | 8 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-46348C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116174706 | ||||||
| chr6:116175001
|
G | A | 44 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0053others(41): Show | 44 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.530-46053G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175001 | ||||||
| chr6:116175387
|
T | C | 20 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(17): Show | 20 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.530-45667T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175387 | ||||||
| chr6:116175412
|
G | A | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.530-45642G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175412 | ||||||
| chr6:116175604
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530-45450C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175604 | ||||||
| chr6:116175619
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-45435T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175619 | ||||||
| chr6:116175736
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-45318A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175736 | ||||||
| chr6:116175762
|
T | C | 4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0052others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-45292T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116175762 | ||||||
| chr6:116176154
|
C | T | 66 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(63): Show | 68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.530-44900C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176154 | ||||||
| chr6:116176540
|
G | A | 1 | a0001c0001t0035g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.530-44514G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176540 | ||||||
| chr6:116176737
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.530-44317A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116176737 | ||||||
| chr6:116177223
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-43831A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177223 | ||||||
| chr6:116177249
|
C | T | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-43805C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177249 | ||||||
| chr6:116177277
|
C | G | 9 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(6): Show | 9 | NA18953.hp2 NA18954.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-43777C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177277 | ||||||
| chr6:116177464
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-43590C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177464 | ||||||
| chr6:116177747
|
T | TG | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0261 | 3 | HG01192.hp2 HG01243.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.530-43307_530-4330 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177747 | ||||||
| chr6:116177842
|
G | A | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017 | 3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.530-43212G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177842 | ||||||
| chr6:116177850
|
A | G | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-43204A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177850 | ||||||
| chr6:116177865
|
G | A | 4 | a0001c0001t0012g0169a0001c0001t0012g0170a0001c0001t0012g0171others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-43189G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177865 | ||||||
| chr6:116177880
|
A | C | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-43174A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177880 | ||||||
| chr6:116177949
|
A | G | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-43105A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116177949 | ||||||
| chr6:116178052
|
A | AGT | 42 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(39): Show | 44 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.530-42966_530-4296 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
A | AGTGT | 8 | a0001c0001t0001g0162a0001c0001t0001g0206a0001c0001t0001g0217others(5): Show | 8 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
A | AGTGTGT | 11 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0208others(8): Show | 11 | HG01074.hp2 HG01192.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0014g0143 | 3 | HG02886.hp2 HG03453.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.530-42972_530-4296 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0228a0001c0001t0007g0132 | 2 | HG02300.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.530-42974_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
AGT | A | 39 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0002g0293others(36): Show | 40 | HG00558.hp2 HG00639.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.530-42966_530-4296 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
AGTGT | A | 27 | a0001c0001t0001g0043a0001c0001t0003g0002a0001c0001t0003g0013others(24): Show | 29 | HG00099.hp2 HG01081.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
AGTGTGT | A | 5 | a0001c0001t0001g0136a0001c0001t0002g0239a0001c0001t0002g0240others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178052
|
AGTGTGTG others(3): Show |
A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.530-42974_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178052 | |||||
| chr6:116178068
|
T | C | 8 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42986T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178068 | ||||||
| chr6:116178070
|
TGTGTGTG others(19): Show |
T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42982_530-4295 others(30): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178070 | |||||
| chr6:116178080
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42974T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178080 | ||||||
| chr6:116178082
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42972T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178082 | ||||||
| chr6:116178082
|
TGTGTGTG others(3): Show |
T | 15 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0245others(12): Show | 15 | HG01099.hp2 HG01515.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-42970_530-4296 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178082 | |||||
| chr6:116178082
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0007g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.530-42970_530-4295 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178082 | |||||
| chr6:116178084
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-42970T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178084 | ||||||
| chr6:116178084
|
TGTGTGCG others(1): Show |
T | 4 | a0001c0001t0008g0258a0001c0001t0015g0284a0001c0001t0015g0289others(1): Show | 4 | HG00738.hp1 HG01934.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-42968_530-4296 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178084 | |||||
| chr6:116178084
|
TGTGTGCG others(5): Show |
T | 1 | a0001c0001t0035g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.530-42968_530-4295 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178084 | |||||
| chr6:116178086
|
T | C | 3 | a0001c0001t0002g0248a0001c0001t0005g0139a0001c0001t0005g0280 | 3 | HG02647.hp2 HG03516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-42968T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178086 | ||||||
| chr6:116178086
|
TGTGC | T | 3 | a0001c0001t0001g0172a0001c0001t0002g0076a0001c0001t0036g0135 | 3 | HG00642.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.530-42966_530-4296 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178086 | |||||
| chr6:116178086
|
TGTGCGCG others(3): Show |
T | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-42966_530-4295 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178086 | |||||
| chr6:116178088
|
T | C | 8 | a0001c0001t0002g0248a0001c0001t0003g0007a0001c0001t0003g0018others(5): Show | 8 | HG01346.hp2 HG02132.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-42966T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178088 | ||||||
| chr6:116178088
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0009g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.530-42965_530-4296 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178088 | |||||
| chr6:116178088
|
TGC | T | 12 | a0001c0001t0001g0075a0001c0001t0001g0119a0001c0001t0001g0121others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-42952_530-4295 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178088 | |||||
| chr6:116178090
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0092others(125): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.530-42964C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178090 | ||||||
| chr6:116178092
|
C | T | 48 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(45): Show | 49 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.530-42962C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178092 | ||||||
| chr6:116178094
|
C | T | 25 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0201others(22): Show | 25 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-42960C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178094 | ||||||
| chr6:116178096
|
C | T | 10 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0068others(7): Show | 10 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-42958C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178096 | ||||||
| chr6:116178096
|
CGCGCGCG others(1): Show |
C | 10 | a0001c0001t0004g0050a0001c0001t0006g0052a0001c0001t0006g0061others(7): Show | 10 | HG01106.hp1 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-42954_530-4294 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178096 | |||||
| chr6:116178098
|
C | T | 11 | a0001c0001t0002g0068a0001c0001t0002g0083a0001c0001t0003g0007others(8): Show | 11 | HG01081.hp1 HG01168.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-42956C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178098 | ||||||
| chr6:116178098
|
CGCGCGT | C | 6 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0058others(3): Show | 6 | HG02976.hp2 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.530-42952_530-4294 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178098 | |||||
| chr6:116178100
|
C | T | 71 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(68): Show | 73 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.530-42954C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178100 | ||||||
| chr6:116178102
|
C | T | 5 | a0001c0001t0003g0007a0001c0001t0004g0040a0001c0001t0005g0134others(2): Show | 5 | HG02895.hp1 HG03239.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-42952C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178102 | ||||||
| chr6:116178102
|
CGT | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0073a0001c0001t0002g0086others(2): Show | 6 | HG01071.hp2 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-42950_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178102 | |||||
| chr6:116178104
|
T | C | 38 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0201others(35): Show | 38 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.530-42950T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178104 | ||||||
| chr6:116178104
|
TGC | T | 8 | a0001c0001t0002g0239a0001c0001t0002g0293a0001c0001t0004g0257others(5): Show | 8 | HG01361.hp2 HG01981.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-42948_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178104 | |||||
| chr6:116178106
|
C | CGT | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-42946_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | |||||
| chr6:116178106
|
C | T | 66 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(63): Show | 68 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.530-42948C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178106 | ||||||
| chr6:116178106
|
CGTGCGT | C | 7 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0006g0005others(4): Show | 8 | HG00642.hp1 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-42944_530-4293 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | |||||
| chr6:116178106
|
CGTGCGTG others(3): Show |
C | 1 | a0001c0001t0008g0258 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.530-42944_530-4293 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178106 | |||||
| chr6:116178108
|
T | C | 10 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0068others(7): Show | 10 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-42946T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178108 | ||||||
| chr6:116178108
|
TGC | T | 29 | a0001c0001t0002g0053a0001c0001t0002g0106a0001c0001t0002g0111others(26): Show | 29 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(26): Show |
intron_variant | MODIFIER | c.530-42944_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178108 | |||||
| chr6:116178110
|
C | CGT | 4 | a0001c0001t0001g0152a0001c0001t0001g0189a0001c0001t0001g0224others(1): Show | 4 | HG01192.hp2 HG03041.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-42921_530-4292 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178110 | |||||
| chr6:116178110
|
C | T | 91 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(88): Show | 93 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.530-42944C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178110 | ||||||
| chr6:116178110
|
CGT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0119a0001c0001t0001g0145others(35): Show | 41 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.530-42921_530-4292 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178110 | |||||
| chr6:116178112
|
T | C | 2 | a0001c0001t0002g0065a0001c0001t0002g0082 | 2 | HG00738.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.530-42942T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178112 | ||||||
| chr6:116178112
|
T | TGC | 9 | a0001c0001t0001g0190a0001c0001t0001g0201a0001c0001t0002g0067others(6): Show | 9 | HG00408.hp1 HG01081.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.530-42941_530-4294 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116178112 | |||||
| chr6:116178114
|
T | C | 10 | a0001c0001t0001g0187a0001c0001t0001g0230a0001c0001t0006g0161others(7): Show | 10 | HG01496.hp2 HG02559.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-42940T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178114 | ||||||
| chr6:116178116
|
T | C | 3 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0018g0127 | 3 | HG02451.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.530-42938T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178116 | ||||||
| chr6:116178118
|
T | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.530-42936T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178118 | ||||||
| chr6:116178122
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.530-42932T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178122 | ||||||
| chr6:116178253
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.530-42801A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178253 | ||||||
| chr6:116178306
|
T | A | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-42748T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178306 | ||||||
| chr6:116178311
|
G | A | 1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.530-42743G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178311 | ||||||
| chr6:116178377
|
T | G | 1 | a0001c0001t0006g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.530-42677T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178377 | ||||||
| chr6:116178415
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42639C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178415 | ||||||
| chr6:116178675
|
T | C | 1 | a0001c0001t0006g0061 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.530-42379T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178675 | ||||||
| chr6:116178704
|
T | C | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-42350T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178704 | ||||||
| chr6:116178785
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02258.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530-42269A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178785 | ||||||
| chr6:116178912
|
G | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-42142G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116178912 | ||||||
| chr6:116179040
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530-42014G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179040 | ||||||
| chr6:116179264
|
A | G | 94 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-41790A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179264 | ||||||
| chr6:116179400
|
G | T | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-41654G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179400 | ||||||
| chr6:116179507
|
T | C | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-41547T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179507 | ||||||
| chr6:116179726
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-41328T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179726 | ||||||
| chr6:116179875
|
C | A | 30 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0003g0002others(27): Show | 32 | HG00408.hp2 HG00558.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.530-41179C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116179875 | ||||||
| chr6:116180017
|
ATCT | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-41035_530-4103 others(7): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116180017 | |||||
| chr6:116180340
|
G | A | 156 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(153): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.530-40714G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180340 | ||||||
| chr6:116180413
|
G | C | 1 | a0001c0001t0004g0254 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.530-40641G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180413 | ||||||
| chr6:116180820
|
G | A | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-40234G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180820 | ||||||
| chr6:116180848
|
T | A | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-40206T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180848 | ||||||
| chr6:116180938
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.530-40116G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116180938 | ||||||
| chr6:116181048
|
C | A | 4 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0007g0131others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-40006C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181048 | ||||||
| chr6:116181063
|
ATTTAC | A | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-39986_530-3998 others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116181063 | |||||
| chr6:116181110
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-39944A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181110 | ||||||
| chr6:116181242
|
A | G | 48 | a0001c0001t0002g0004a0001c0001t0002g0054a0001c0001t0002g0055others(45): Show | 50 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.530-39812A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181242 | ||||||
| chr6:116181520
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.530-39534G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181520 | ||||||
| chr6:116181680
|
T | C | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-39374T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181680 | ||||||
| chr6:116181775
|
C | CTA | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-39275_530-3927 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116181775 | |||||
| chr6:116181939
|
T | A | 1 | a0001c0001t0002g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.530-39115T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116181939 | ||||||
| chr6:116182005
|
C | T | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-39049C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182005 | ||||||
| chr6:116182039
|
C | T | 2 | a0001c0001t0009g0278a0001c0001t0009g0290 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.530-39015C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182039 | ||||||
| chr6:116182222
|
A | AGAGAGAG others(13): Show |
1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530-38831_530-3883 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGAGAG others(15): Show |
1 | a0001c0001t0020g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.530-38831_530-3883 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGAGTG others(9): Show |
3 | a0001c0001t0002g0266a0001c0001t0003g0013a0001c0001t0003g0042 | 3 | HG02965.hp1 NA18522.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.530-38831_530-3883 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGTGTG others(7): Show |
1 | a0001c0001t0004g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.530-38831_530-3883 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGTGTG others(9): Show |
79 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.530-38831_530-3883 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGTGTG others(11): Show |
9 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 10 | HG02896.hp1 HG03098.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-38831_530-3883 others(22): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGAGTGTG others(13): Show |
1 | a0001c0001t0005g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.530-38831_530-3883 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGT | 40 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0124others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.530-38801_530-3880 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGT | 5 | a0001c0001t0001g0125a0001c0001t0001g0217a0001c0001t0002g0076others(2): Show | 5 | HG00642.hp1 HG01258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-38803_530-3880 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGTGT | 4 | a0001c0001t0002g0248a0001c0001t0006g0005a0001c0001t0014g0247others(1): Show | 5 | HG02145.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-38805_530-3880 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGTGTG others(3): Show |
14 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0106others(11): Show | 14 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-38809_530-3880 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0005g0280 | 3 | HG01884.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.530-38811_530-3880 others(16): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGTGTG others(7): Show |
7 | a0001c0001t0002g0057a0001c0001t0002g0279a0001c0001t0003g0291others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-38813_530-3880 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
A | AGTGTGTG others(9): Show |
1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530-38815_530-3880 others(20): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
AGT | A | 19 | a0001c0001t0002g0051a0001c0001t0006g0052a0001c0001t0006g0058others(16): Show | 19 | HG00642.hp2 HG00741.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.530-38801_530-3880 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182222
|
AGTGTGT | A | 3 | a0001c0001t0002g0083a0001c0001t0009g0144a0003c0004t0002g0079 | 3 | HG01081.hp1 HG01361.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.530-38805_530-3880 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182222 | |||||
| chr6:116182235
|
G | A | 90 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(87): Show | 92 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.530-38819G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182235 | ||||||
| chr6:116182392
|
G | A | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-38662G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182392 | ||||||
| chr6:116182526
|
C | T | 38 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(35): Show | 40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-38528C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182526 | ||||||
| chr6:116182553
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.530-38501T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182553 | ||||||
| chr6:116182581
|
G | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-38473G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182581 | ||||||
| chr6:116182673
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.530-38381T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116182673 | ||||||
| chr6:116182746
|
TTGCTGAT others(1): Show |
T | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-38305_530-3829 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116182746 | |||||
| chr6:116183310
|
T | C | 93 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0053others(90): Show | 95 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.530-37744T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183310 | ||||||
| chr6:116183348
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.530-37706G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183348 | ||||||
| chr6:116183646
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.530-37408A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183646 | ||||||
| chr6:116183761
|
A | G | 1 | a0001c0001t0021g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.530-37293A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183761 | ||||||
| chr6:116183783
|
T | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-37271T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183783 | ||||||
| chr6:116183828
|
T | C | 1 | a0001c0001t0003g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.530-37226T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116183828 | ||||||
| chr6:116184048
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.530-37006G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184048 | ||||||
| chr6:116184124
|
T | C | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-36930T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184124 | ||||||
| chr6:116184222
|
A | G | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-36832A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184222 | ||||||
| chr6:116184451
|
G | C | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-36603G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184451 | ||||||
| chr6:116184455
|
A | G | 1 | a0001c0001t0004g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-36599A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184455 | ||||||
| chr6:116184506
|
C | T | 38 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(35): Show | 40 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-36548C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184506 | ||||||
| chr6:116184574
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0156a0001c0001t0001g0159others(11): Show | 16 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(13): Show |
intron_variant | MODIFIER | c.530-36480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184574 | ||||||
| chr6:116184632
|
G | A | 156 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0004others(153): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.530-36422G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184632 | ||||||
| chr6:116184776
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-36278T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116184776 | ||||||
| chr6:116184914
|
TG | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0156a0001c0001t0001g0159others(10): Show | 15 | HG00558.hp1 NA18942.hp1 NA18957.hp2 others(12): Show |
intron_variant | MODIFIER | c.530-36137delG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116184914 | |||||
| chr6:116185082
|
A | T | 45 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(42): Show | 47 | HG00408.hp2 HG00558.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.530-35972A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185082 | ||||||
| chr6:116185139
|
A | C | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-35915A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185139 | ||||||
| chr6:116185212
|
A | G | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-35842A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185212 | ||||||
| chr6:116185387
|
A | G | 3 | a0001c0001t0013g0070a0001c0001t0013g0071a0001c0001t0013g0072 | 3 | HG02615.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.530-35667A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185387 | ||||||
| chr6:116185437
|
C | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35617C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185437 | ||||||
| chr6:116185441
|
T | G | 1 | a0001c0001t0003g0191 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.530-35613T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185441 | ||||||
| chr6:116185558
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35496C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185558 | ||||||
| chr6:116185655
|
G | A | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.530-35399G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185655 | ||||||
| chr6:116185809
|
C | A | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.530-35245C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116185809 | ||||||
| chr6:116186039
|
T | C | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-35015T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186039 | ||||||
| chr6:116186043
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-35011G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186043 | ||||||
| chr6:116186080
|
G | A | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-34974G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186080 | ||||||
| chr6:116186450
|
C | T | 1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.530-34604C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186450 | ||||||
| chr6:116186468
|
T | C | 11 | a0001c0001t0003g0049a0001c0001t0004g0050a0001c0001t0006g0009others(8): Show | 11 | HG00642.hp2 HG01106.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-34586T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186468 | ||||||
| chr6:116186512
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.530-34542G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186512 | ||||||
| chr6:116186518
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.530-34536C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186518 | ||||||
| chr6:116186642
|
T | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-34412T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186642 | ||||||
| chr6:116186660
|
G | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-34394G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116186660 | ||||||
| chr6:116187042
|
T | C | 65 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0098others(62): Show | 67 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.530-34012T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187042 | ||||||
| chr6:116187150
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0239others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-33904A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187150 | ||||||
| chr6:116187207
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530-33847T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187207 | ||||||
| chr6:116187275
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-33779G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187275 | ||||||
| chr6:116187349
|
A | G | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-33705A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187349 | ||||||
| chr6:116187542
|
G | A | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-33512G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187542 | ||||||
| chr6:116187595
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-33459A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187595 | ||||||
| chr6:116187597
|
G | A | 2 | a0001c0001t0002g0264a0001c0001t0002g0275 | 2 | NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.530-33457G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187597 | ||||||
| chr6:116187620
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-33434G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187620 | ||||||
| chr6:116187812
|
T | C | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-33242T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187812 | ||||||
| chr6:116187855
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-33199T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187855 | ||||||
| chr6:116187880
|
G | A | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017 | 3 | HG01258.hp1 HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.530-33174G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116187880 | ||||||
| chr6:116188137
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.530-32917A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188137 | ||||||
| chr6:116188390
|
G | A | 10 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-32664G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188390 | ||||||
| chr6:116188439
|
T | A | 1 | a0001c0001t0003g0038 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.530-32615T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188439 | ||||||
| chr6:116188473
|
C | T | 94 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0002g0047others(91): Show | 96 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.530-32581C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188473 | ||||||
| chr6:116188477
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.530-32577A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188477 | ||||||
| chr6:116188513
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0211others(1): Show | 4 | HG01167.hp2 HG01261.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-32541A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188513 | ||||||
| chr6:116188526
|
C | A | 1 | a0001c0001t0003g0038 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.530-32528C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188526 | ||||||
| chr6:116188542
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-32512A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188542 | ||||||
| chr6:116188706
|
C | CT | 158 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0001g0201others(155): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.530-32335dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116188706 | |||||
| chr6:116188888
|
G | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-32166G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116188888 | ||||||
| chr6:116189177
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.530-31877C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189177 | ||||||
| chr6:116189229
|
A | G | 3 | a0001c0001t0006g0005a0001c0001t0014g0247a0001c0001t0018g0276 | 4 | HG02145.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-31825A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189229 | ||||||
| chr6:116189396
|
G | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-31658G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189396 | ||||||
| chr6:116189475
|
A | G | 1 | a0001c0001t0002g0275 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.530-31579A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189475 | ||||||
| chr6:116189779
|
C | G | 1 | a0001c0001t0005g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.530-31275C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189779 | ||||||
| chr6:116189844
|
A | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0279others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-31210A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116189844 | ||||||
| chr6:116190127
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.530-30927A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190127 | ||||||
| chr6:116190481
|
G | A | 11 | a0001c0001t0003g0291a0001c0001t0006g0118a0001c0001t0006g0161others(8): Show | 11 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-30573G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190481 | ||||||
| chr6:116190541
|
G | T | 1 | a0001c0001t0002g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.530-30513G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190541 | ||||||
| chr6:116190861
|
A | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0189 | 2 | NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.530-30193A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190861 | ||||||
| chr6:116190956
|
A | G | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-30098A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116190956 | ||||||
| chr6:116191032
|
C | T | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-30022C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191032 | ||||||
| chr6:116191177
|
C | G | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-29877C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191177 | ||||||
| chr6:116191459
|
G | A | 2 | a0001c0001t0003g0291a0001c0001t0006g0118 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.530-29595G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191459 | ||||||
| chr6:116191513
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.530-29541A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191513 | ||||||
| chr6:116191611
|
T | C | 7 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 8 | NA18947.hp1 NA18957.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-29443T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191611 | ||||||
| chr6:116191697
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.530-29357C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191697 | ||||||
| chr6:116191909
|
A | G | 1 | a0001c0001t0039g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.530-29145A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191909 | ||||||
| chr6:116191959
|
G | C | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-29095G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116191959 | ||||||
| chr6:116192065
|
G | T | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-28989G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192065 | ||||||
| chr6:116192157
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.530-28897G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192157 | ||||||
| chr6:116192321
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0003g0026 | 2 | NA18973.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.530-28733A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192321 | ||||||
| chr6:116192350
|
C | A | 14 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0003g0112others(11): Show | 14 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-28704C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192350 | ||||||
| chr6:116192501
|
T | C | 3 | a0001c0001t0002g0293a0001c0001t0017g0059a0001c0001t0017g0294 | 3 | HG01981.hp2 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-28553T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192501 | ||||||
| chr6:116192515
|
G | A | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0263others(20): Show | 24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-28539G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192515 | ||||||
| chr6:116192749
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.530-28305T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192749 | ||||||
| chr6:116192791
|
T | A | 161 | a0001c0001t0001g0043a0001c0001t0001g0119a0001c0001t0001g0121others(158): Show | 165 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.530-28263T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192791 | ||||||
| chr6:116192874
|
G | C | 1 | a0001c0001t0032g0243 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.530-28180G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192874 | ||||||
| chr6:116192883
|
C | A | 20 | a0001c0001t0001g0119a0001c0001t0002g0056a0001c0001t0005g0134others(17): Show | 20 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.530-28171C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116192883 | ||||||
| chr6:116193090
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0093others(255): Show | 264 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.530-27964A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193090 | ||||||
| chr6:116193104
|
T | C | 16 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-27950T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193104 | ||||||
| chr6:116193355
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-27699A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193355 | ||||||
| chr6:116193497
|
T | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | NA18947.hp2 NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.530-27557T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193497 | ||||||
| chr6:116193629
|
G | A | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-27425G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193629 | ||||||
| chr6:116193700
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.530-27354A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193700 | ||||||
| chr6:116193765
|
TTAAAAA | T | 165 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(162): Show | 168 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.530-27282_530-2727 others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116193765 | |||||
| chr6:116193837
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.530-27217G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193837 | ||||||
| chr6:116193899
|
A | G | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-27155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116193899 | ||||||
| chr6:116194029
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-27025A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194029 | ||||||
| chr6:116194061
|
C | A | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-26993C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194061 | ||||||
| chr6:116194170
|
T | G | 1 | a0001c0001t0004g0255 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530-26884T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194170 | ||||||
| chr6:116194499
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.530-26555T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194499 | ||||||
| chr6:116194607
|
G | A | 1 | a0001c0001t0007g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-26447G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194607 | ||||||
| chr6:116194626
|
A | G | 8 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-26428A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194626 | ||||||
| chr6:116194662
|
A | T | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.530-26392A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194662 | ||||||
| chr6:116194721
|
G | A | 23 | a0001c0001t0003g0007a0001c0001t0003g0288a0001c0001t0004g0155others(20): Show | 23 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-26333G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194721 | ||||||
| chr6:116194779
|
G | A | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.530-26275G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194779 | ||||||
| chr6:116194979
|
G | A | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-26075G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116194979 | ||||||
| chr6:116195282
|
C | T | 24 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(21): Show | 25 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-25772C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195282 | ||||||
| chr6:116195687
|
G | C | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0002c0002t0002g0069others(1): Show | 4 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-25367G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195687 | ||||||
| chr6:116195894
|
A | G | 8 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.530-25160A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195894 | ||||||
| chr6:116195998
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-25056G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116195998 | ||||||
| chr6:116196208
|
A | G | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-24846A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196208 | ||||||
| chr6:116196244
|
T | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(2): Show | 5 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-24810T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196244 | ||||||
| chr6:116196278
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-24776A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196278 | ||||||
| chr6:116196445
|
T | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-24609T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196445 | ||||||
| chr6:116196482
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530-24572G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196482 | ||||||
| chr6:116196521
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.530-24533G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196521 | ||||||
| chr6:116196588
|
A | G | 2 | a0001c0001t0017g0059a0001c0001t0017g0294 | 2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-24466A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196588 | ||||||
| chr6:116196688
|
T | C | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-24366T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196688 | ||||||
| chr6:116196772
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-24282A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196772 | ||||||
| chr6:116196791
|
G | C | 1 | a0001c0001t0017g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530-24263G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196791 | ||||||
| chr6:116196807
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.530-24247G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196807 | ||||||
| chr6:116196925
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-24129A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116196925 | ||||||
| chr6:116197032
|
C | T | 4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0052others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-24022C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197032 | ||||||
| chr6:116197440
|
G | A | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-23614G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197440 | ||||||
| chr6:116197450
|
G | A | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-23604G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197450 | ||||||
| chr6:116197663
|
G | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.530-23391G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197663 | ||||||
| chr6:116197821
|
A | G | 1 | a0001c0001t0004g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.530-23233A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197821 | ||||||
| chr6:116197889
|
CAT | C | 24 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(21): Show | 24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-23164_530-2316 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116197889 | ||||||
| chr6:116198030
|
A | T | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-23024A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198030 | ||||||
| chr6:116198281
|
T | C | 34 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0012others(31): Show | 36 | HG00408.hp2 HG00558.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.530-22773T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198281 | ||||||
| chr6:116198408
|
A | G | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-22646A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198408 | ||||||
| chr6:116198477
|
A | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-22577A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116198477 | ||||||
| chr6:116199024
|
A | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-22030A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199024 | ||||||
| chr6:116199150
|
G | A | 1 | a0001c0001t0006g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.530-21904G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199150 | ||||||
| chr6:116199185
|
C | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-21869C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199185 | ||||||
| chr6:116199822
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-21232G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199822 | ||||||
| chr6:116199996
|
A | AG | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-21058_530-2105 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199996 | ||||||
| chr6:116199997
|
A | AG | 23 | a0001c0001t0002g0239a0001c0001t0002g0266a0001c0001t0007g0140others(20): Show | 23 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-21056dupG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | |||||
| chr6:116199997
|
A | AGC | 6 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0007g0131others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-21056_530-2105 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | |||||
| chr6:116199997
|
A | AGG | 15 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(12): Show | 16 | HG00642.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-21056_530-2105 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116199997 | |||||
| chr6:116199997
|
A | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-21057A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199997 | ||||||
| chr6:116199998
|
GT | G | 26 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.530-21055delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199998 | ||||||
| chr6:116199999
|
T | G | 161 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0055others(158): Show | 164 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.530-21055T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116199999 | ||||||
| chr6:116200001
|
G | GC | 78 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(75): Show | 80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.530-21053_530-2105 others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200001 | ||||||
| chr6:116200001
|
G | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-21053G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200001 | ||||||
| chr6:116200023
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-21031G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200023 | ||||||
| chr6:116200027
|
G | A | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-21027G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200027 | ||||||
| chr6:116200499
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0189 | 2 | NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.530-20555A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200499 | ||||||
| chr6:116200858
|
C | A | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-20196C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116200858 | ||||||
| chr6:116201452
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-19602G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116201452 | ||||||
| chr6:116201672
|
C | A | 1 | a0001c0001t0003g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.530-19382C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116201672 | ||||||
| chr6:116202103
|
T | G | 1 | a0001c0001t0004g0249 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.530-18951T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202103 | ||||||
| chr6:116202292
|
C | T | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.530-18762C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202292 | ||||||
| chr6:116202477
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.530-18577A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202477 | ||||||
| chr6:116202685
|
A | T | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-18369A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202685 | ||||||
| chr6:116202747
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.530-18307T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116202747 | ||||||
| chr6:116203100
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-17954A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203100 | ||||||
| chr6:116203136
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.530-17918A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203136 | ||||||
| chr6:116203154
|
T | G | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-17900T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203154 | ||||||
| chr6:116203239
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0282 | 3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.530-17815C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203239 | ||||||
| chr6:116203363
|
A | G | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-17691A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203363 | ||||||
| chr6:116203440
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.530-17614T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203440 | ||||||
| chr6:116203454
|
T | C | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-17600T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203454 | ||||||
| chr6:116203518
|
A | G | 5 | a0001c0001t0003g0013a0001c0001t0003g0028a0001c0001t0003g0039others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-17536A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203518 | ||||||
| chr6:116203610
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0041 | 2 | NA18942.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.530-17444T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203610 | ||||||
| chr6:116203713
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0282 | 3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.530-17341A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116203713 | ||||||
| chr6:116204106
|
C | T | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-16948C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204106 | ||||||
| chr6:116204113
|
A | G | 1 | a0001c0001t0017g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530-16941A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204113 | ||||||
| chr6:116204138
|
A | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.530-16916A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204138 | ||||||
| chr6:116204260
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-16794A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204260 | ||||||
| chr6:116204346
|
T | C | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-16708T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204346 | ||||||
| chr6:116204426
|
C | T | 1 | a0001c0001t0007g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-16628C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204426 | ||||||
| chr6:116204442
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(286): Show | 295 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.530-16612C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204442 | ||||||
| chr6:116204490
|
A | G | 2 | a0002c0002t0002g0069a0002c0002t0002g0081 | 2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.530-16564A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204490 | ||||||
| chr6:116204589
|
A | G | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-16465A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204589 | ||||||
| chr6:116204605
|
G | A | 1 | a0001c0001t0019g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-16449G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204605 | ||||||
| chr6:116204757
|
C | T | 1 | a0001c0001t0006g0009 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.530-16297C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204757 | ||||||
| chr6:116204768
|
T | C | 4 | a0001c0001t0012g0169a0001c0001t0012g0170a0001c0001t0012g0171others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-16286T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116204768 | ||||||
| chr6:116205018
|
A | G | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-16036A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205018 | ||||||
| chr6:116205195
|
A | T | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-15859A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205195 | ||||||
| chr6:116205246
|
T | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-15808T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205246 | ||||||
| chr6:116205412
|
C | T | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.530-15642C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205412 | ||||||
| chr6:116205480
|
TA | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-15572delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116205480 | |||||
| chr6:116205599
|
T | TG | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-15448dupG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116205599 | |||||
| chr6:116205754
|
T | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-15300T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205754 | ||||||
| chr6:116205849
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0221 | 2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.530-15205A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205849 | ||||||
| chr6:116205957
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-15097A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205957 | ||||||
| chr6:116205981
|
C | T | 1 | a0001c0001t0003g0046 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.530-15073C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116205981 | ||||||
| chr6:116206369
|
T | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-14685T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206369 | ||||||
| chr6:116206422
|
T | C | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-14632T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206422 | ||||||
| chr6:116206571
|
T | A | 1 | a0001c0001t0003g0025 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.530-14483T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206571 | ||||||
| chr6:116206770
|
T | C | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-14284T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206770 | ||||||
| chr6:116206952
|
T | C | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-14102T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116206952 | ||||||
| chr6:116207018
|
GTC | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-14034_530-1403 others(6): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207018 | |||||
| chr6:116207035
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.530-14019A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207035 | ||||||
| chr6:116207298
|
ATAGAGTC | A | 138 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(135): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.530-13753_530-1374 others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207298 | |||||
| chr6:116207306
|
T | G | 138 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(135): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.530-13748T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207306 | ||||||
| chr6:116207370
|
C | CA | 288 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(285): Show | 294 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.530-13676dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116207370 | |||||
| chr6:116207430
|
A | G | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-13624A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207430 | ||||||
| chr6:116207485
|
G | A | 24 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(21): Show | 24 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.530-13569G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207485 | ||||||
| chr6:116207703
|
A | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-13351A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207703 | ||||||
| chr6:116207816
|
C | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-13238C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207816 | ||||||
| chr6:116207877
|
C | T | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-13177C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207877 | ||||||
| chr6:116207899
|
A | G | 2 | a0001c0001t0002g0269a0001c0001t0002g0274 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.530-13155A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207899 | ||||||
| chr6:116207951
|
T | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-13103T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116207951 | ||||||
| chr6:116208032
|
C | CT | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-13019dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116208032 | |||||
| chr6:116208529
|
G | A | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-12525G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116208529 | ||||||
| chr6:116208845
|
G | A | 1 | a0001c0001t0004g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-12209G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116208845 | ||||||
| chr6:116209038
|
G | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-12016G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209038 | ||||||
| chr6:116209141
|
C | T | 21 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(18): Show | 21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.530-11913C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209141 | ||||||
| chr6:116209344
|
A | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-11710A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209344 | ||||||
| chr6:116209604
|
T | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-11450T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209604 | ||||||
| chr6:116209632
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-11422A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209632 | ||||||
| chr6:116209693
|
G | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-11361G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209693 | ||||||
| chr6:116209819
|
C | G | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-11235C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116209819 | ||||||
| chr6:116210146
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.530-10908C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210146 | ||||||
| chr6:116210211
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.530-10843A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210211 | ||||||
| chr6:116210366
|
GA | G | 24 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-10677delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116210366 | |||||
| chr6:116210438
|
G | T | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-10616G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210438 | ||||||
| chr6:116210465
|
A | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-10589A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210465 | ||||||
| chr6:116210745
|
AAAAT | A | 24 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(21): Show | 25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.530-10304_530-1030 others(8): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116210745 | |||||
| chr6:116210781
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.530-10273A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210781 | ||||||
| chr6:116210905
|
G | T | 12 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(9): Show | 13 | HG00642.hp2 HG02717.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.530-10149G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116210905 | ||||||
| chr6:116211052
|
A | G | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.530-10002A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211052 | ||||||
| chr6:116211102
|
C | A | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.530-9952C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211102 | ||||||
| chr6:116211247
|
C | T | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-9807C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211247 | ||||||
| chr6:116211267
|
C | T | 26 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.530-9787C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211267 | ||||||
| chr6:116211696
|
C | T | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-9358C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211696 | ||||||
| chr6:116211937
|
G | A | 1 | a0001c0001t0013g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.530-9117G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211937 | ||||||
| chr6:116211951
|
C | T | 1 | a0001c0001t0006g0005 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.530-9103C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211951 | ||||||
| chr6:116211953
|
G | C | 208 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(205): Show | 212 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.530-9101G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116211953 | ||||||
| chr6:116212220
|
TATC | T | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.530-8831_530-8829d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116212220 | |||||
| chr6:116212466
|
G | A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-8588G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116212466 | ||||||
| chr6:116212848
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.530-8206G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116212848 | ||||||
| chr6:116213065
|
G | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-7989G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213065 | ||||||
| chr6:116213083
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-7971A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213083 | ||||||
| chr6:116213129
|
A | T | 1 | a0001c0001t0004g0255 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530-7925A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213129 | ||||||
| chr6:116213272
|
A | C | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530-7782A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213272 | ||||||
| chr6:116213434
|
C | T | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.530-7620C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213434 | ||||||
| chr6:116213464
|
C | G | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.530-7590C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213464 | ||||||
| chr6:116213548
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-7506A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213548 | ||||||
| chr6:116213665
|
T | C | 2 | a0001c0001t0007g0246a0001c0001t0035g0292 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.530-7389T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213665 | ||||||
| chr6:116213773
|
A | G | 1 | a0001c0001t0007g0131 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.530-7281A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213773 | ||||||
| chr6:116213887
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.530-7167T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116213887 | ||||||
| chr6:116214081
|
T | G | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.530-6973T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214081 | ||||||
| chr6:116214217
|
C | G | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.530-6837C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214217 | ||||||
| chr6:116214240
|
T | C | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-6814T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214240 | ||||||
| chr6:116214292
|
A | G | 7 | a0001c0001t0004g0155a0001c0001t0004g0164a0001c0001t0004g0166others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-6762A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214292 | ||||||
| chr6:116214470
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-6584A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214470 | ||||||
| chr6:116214535
|
C | G | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.530-6519C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214535 | ||||||
| chr6:116214808
|
C | T | 2 | a0001c0001t0002g0083a0003c0004t0002g0079 | 2 | HG01081.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.530-6246C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116214808 | ||||||
| chr6:116214820
|
TA | T | 11 | a0001c0001t0006g0118a0001c0001t0006g0161a0001c0001t0007g0129others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-6223delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116214820 | |||||
| chr6:116215088
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-5966A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215088 | ||||||
| chr6:116215449
|
T | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-5605T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215449 | ||||||
| chr6:116215591
|
T | A | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.530-5463T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215591 | ||||||
| chr6:116215761
|
C | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-5293C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215761 | ||||||
| chr6:116215861
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.530-5193G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215861 | ||||||
| chr6:116215946
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.530-5108G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116215946 | ||||||
| chr6:116216013
|
T | A | 1 | a0001c0001t0003g0019 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.530-5041T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216013 | ||||||
| chr6:116216075
|
C | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-4979C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216075 | ||||||
| chr6:116216155
|
A | T | 1 | a0001c0003t0014g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.530-4899A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216155 | ||||||
| chr6:116216326
|
T | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-4728T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216326 | ||||||
| chr6:116216335
|
T | A | 1 | a0001c0001t0008g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.530-4719T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216335 | ||||||
| chr6:116216392
|
T | TA | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-4651dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116216392 | |||||
| chr6:116216568
|
T | C | 7 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(4): Show | 7 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-4486T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216568 | ||||||
| chr6:116216587
|
A | G | 1 | a0001c0001t0020g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530-4467A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216587 | ||||||
| chr6:116216743
|
A | C | 1 | a0001c0001t0019g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-4311A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216743 | ||||||
| chr6:116216851
|
C | G | 2 | a0001c0001t0017g0059a0001c0001t0017g0294 | 2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.530-4203C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216851 | ||||||
| chr6:116216888
|
A | G | 1 | a0001c0001t0004g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.530-4166A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116216888 | ||||||
| chr6:116217022
|
C | T | 4 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-4032C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217022 | ||||||
| chr6:116217026
|
G | A | 1 | a0001c0001t0007g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-4028G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217026 | ||||||
| chr6:116217161
|
AATATTCA others(6): Show |
A | 2 | a0001c0001t0003g0191a0001c0001t0003g0205 | 2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.530-3891_530-3879d others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116217161 | |||||
| chr6:116217210
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.530-3844T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217210 | ||||||
| chr6:116217371
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530-3683G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217371 | ||||||
| chr6:116217923
|
T | C | 141 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(138): Show | 144 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.530-3131T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116217923 | ||||||
| chr6:116218227
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.530-2827C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218227 | ||||||
| chr6:116218228
|
G | A | 100 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(97): Show | 102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.530-2826G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218228 | ||||||
| chr6:116218469
|
G | T | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-2585G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218469 | ||||||
| chr6:116218538
|
A | T | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.530-2516A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218538 | ||||||
| chr6:116218803
|
C | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0002g0279 | 3 | HG02486.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.530-2251C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218803 | ||||||
| chr6:116218834
|
CA | C | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-2219delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218834 | ||||||
| chr6:116218954
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530-2100G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116218954 | ||||||
| chr6:116219041
|
G | A | 1 | a0001c0001t0018g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530-2013G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219041 | ||||||
| chr6:116219232
|
C | T | 23 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0066others(20): Show | 24 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.530-1822C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219232 | ||||||
| chr6:116219477
|
T | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.530-1577T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219477 | ||||||
| chr6:116219547
|
A | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.530-1507A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219547 | ||||||
| chr6:116219643
|
C | T | 3 | a0001c0001t0016g0116a0001c0001t0016g0117a0001c0001t0025g0115 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.530-1411C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219643 | ||||||
| chr6:116219679
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-1375A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219679 | ||||||
| chr6:116219719
|
G | A | 1 | a0001c0001t0006g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.530-1335G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219719 | ||||||
| chr6:116219894
|
G | A | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-1160G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219894 | ||||||
| chr6:116219961
|
C | CA | 53 | a0001c0001t0001g0043a0001c0001t0001g0092a0001c0001t0001g0093others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.530-1070dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | |||||
| chr6:116219961
|
CAA | C | 11 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-1071_530-1070d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | |||||
| chr6:116219961
|
CAAA | C | 7 | a0001c0001t0001g0165a0001c0001t0001g0212a0001c0001t0001g0285others(4): Show | 7 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-1072_530-1070d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219961 | |||||
| chr6:116219974
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0008g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530-1077_530-1067d others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219974 | |||||
| chr6:116219983
|
AAC | A | 27 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0061others(24): Show | 27 | HG00642.hp2 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.530-1069_530-1068d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116219983 | |||||
| chr6:116219984
|
AC | A | 40 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0055others(37): Show | 42 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.530-1069delC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219984 | ||||||
| chr6:116219985
|
C | A | 121 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(118): Show | 123 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.530-1069C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116219985 | ||||||
| chr6:116220002
|
G | A | 1 | a0001c0001t0007g0062 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530-1052G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220002 | ||||||
| chr6:116220049
|
C | T | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.530-1005C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220049 | ||||||
| chr6:116220122
|
C | CT | 27 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0121others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.530-909dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | CTT | 68 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0015others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.530-910_530-909dup others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | CTTT | 16 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0012others(13): Show | 17 | HG00438.hp2 HG01175.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.530-911_530-909dup others(3): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(2): Show | 5 | HG01884.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-918_530-909dup others(10): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0064a0001c0001t0002g0279 | 2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.530-919_530-909dup others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0002g0054a0001c0001t0002g0063a0001c0001t0002g0106others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-920_530-909dup others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220122
|
C | T | 10 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(7): Show | 11 | HG00642.hp2 HG02717.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.530-932C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220122 | ||||||
| chr6:116220122
|
CTT | C | 22 | a0001c0001t0002g0004a0001c0001t0002g0065a0001c0001t0002g0067others(19): Show | 23 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.530-910_530-909del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220122 | |||||
| chr6:116220213
|
C | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-841C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220213 | ||||||
| chr6:116220221
|
A | G | 29 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(26): Show | 30 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.530-833A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220221 | ||||||
| chr6:116220340
|
T | C | 189 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(186): Show | 193 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.530-714T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220340 | ||||||
| chr6:116220384
|
C | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.530-670C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220384 | ||||||
| chr6:116220556
|
C | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0240 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.530-498C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220556 | ||||||
| chr6:116220828
|
TAGCC | T | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.530-222_530-219del others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr6 | 116220828 | |||||
| chr6:116220844
|
T | C | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.530-210T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220844 | ||||||
| chr6:116220853
|
A | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-201A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220853 | ||||||
| chr6:116220865
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG00558.hp1 NA18961.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-189T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 6/11 | chr6 | 116220865 | ||||||
| chr6:116221337
|
T | C | 26 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.704+109T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221337 | ||||||
| chr6:116221479
|
C | G | 1 | a0001c0001t0006g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704+251C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221479 | ||||||
| chr6:116221816
|
A | G | 1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.704+588A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221816 | ||||||
| chr6:116221923
|
A | T | 1 | a0001c0001t0004g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.704+695A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116221923 | ||||||
| chr6:116222115
|
A | G | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704+887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222115 | ||||||
| chr6:116222263
|
G | T | 1 | a0001c0001t0010g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.705-771G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222263 | ||||||
| chr6:116222442
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.705-592G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222442 | ||||||
| chr6:116222485
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.705-549T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222485 | ||||||
| chr6:116222644
|
A | C | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.705-390A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222644 | ||||||
| chr6:116222661
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705-373C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222661 | ||||||
| chr6:116222684
|
A | G | 163 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(160): Show | 166 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.705-350A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222684 | ||||||
| chr6:116222720
|
A | C | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.705-314A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222720 | ||||||
| chr6:116222782
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.705-252A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222782 | ||||||
| chr6:116222872
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.705-162A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222872 | ||||||
| chr6:116222892
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0177a0001c0001t0001g0282 | 3 | HG03654.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.705-142T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222892 | ||||||
| chr6:116222931
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.705-103G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 7/11 | chr6 | 116222931 | ||||||
| chr6:116223450
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.802+319G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223450 | ||||||
| chr6:116223574
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+443G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223574 | ||||||
| chr6:116223579
|
G | A | 7 | a0001c0001t0004g0155a0001c0001t0004g0164a0001c0001t0004g0166others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+448G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223579 | ||||||
| chr6:116223587
|
T | A | 2 | a0001c0001t0002g0241a0001c0001t0002g0242 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.802+456T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116223587 | ||||||
| chr6:116224322
|
A | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.802+1191A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224322 | ||||||
| chr6:116224486
|
A | G | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.802+1355A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224486 | ||||||
| chr6:116224545
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.802+1414G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224545 | ||||||
| chr6:116224581
|
T | C | 1 | a0001c0001t0003g0291 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+1450T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224581 | ||||||
| chr6:116224607
|
T | C | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.802+1476T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224607 | ||||||
| chr6:116224749
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.802+1618G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224749 | ||||||
| chr6:116224749
|
G | T | 6 | a0001c0001t0002g0098a0001c0001t0002g0239a0001c0001t0002g0240others(3): Show | 6 | HG02109.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+1618G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224749 | ||||||
| chr6:116224844
|
G | A | 8 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+1713G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116224844 | ||||||
| chr6:116225093
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+1962A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225093 | ||||||
| chr6:116225119
|
C | T | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.802+1988C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225119 | ||||||
| chr6:116225330
|
T | C | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802+2199T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225330 | ||||||
| chr6:116225371
|
A | G | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+2240A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225371 | ||||||
| chr6:116225380
|
A | G | 26 | a0001c0001t0002g0004a0001c0001t0002g0051a0001c0001t0002g0065others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.802+2249A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225380 | ||||||
| chr6:116225689
|
G | C | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.802+2558G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225689 | ||||||
| chr6:116225703
|
G | T | 4 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+2572G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225703 | ||||||
| chr6:116225761
|
A | G | 190 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0051others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.802+2630A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225761 | ||||||
| chr6:116225803
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+2672A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225803 | ||||||
| chr6:116225806
|
G | A | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.802+2675G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225806 | ||||||
| chr6:116225849
|
T | A | 1 | a0001c0001t0005g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.802+2718T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225849 | ||||||
| chr6:116225936
|
G | C | 5 | a0001c0001t0003g0013a0001c0001t0003g0028a0001c0001t0003g0039others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+2805G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116225936 | ||||||
| chr6:116226045
|
A | T | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.802+2914A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226045 | ||||||
| chr6:116226077
|
T | C | 98 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(95): Show | 100 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.802+2946T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226077 | ||||||
| chr6:116226109
|
A | G | 16 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+2978A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226109 | ||||||
| chr6:116226307
|
C | T | 1 | a0001c0001t0008g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.802+3176C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226307 | ||||||
| chr6:116226412
|
GT | G | 11 | a0001c0001t0009g0107a0001c0001t0009g0109a0001c0001t0009g0110others(8): Show | 11 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+3289delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116226412 | |||||
| chr6:116226426
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.802+3295G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226426 | ||||||
| chr6:116226692
|
T | C | 1 | a0001c0001t0037g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802+3561T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226692 | ||||||
| chr6:116226806
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0212others(5): Show | 8 | HG00738.hp1 HG02074.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+3675G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226806 | ||||||
| chr6:116226878
|
A | C | 1 | a0001c0001t0026g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.802+3747A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116226878 | ||||||
| chr6:116227000
|
A | G | 2 | a0001c0001t0009g0107a0001c0001t0009g0144 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.802+3869A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227000 | ||||||
| chr6:116227065
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802+3934T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227065 | ||||||
| chr6:116227077
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+3946G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227077 | ||||||
| chr6:116227281
|
ATGT | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0222 | 3 | NA18959.hp1 NA19002.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.802+4154_802+4156d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116227281 | |||||
| chr6:116227665
|
A | ATGAGGTG others(22): Show |
1 | a0001c0001t0014g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.802+4537_802+4565d others(31): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116227665 | |||||
| chr6:116227728
|
T | C | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.802+4597T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227728 | ||||||
| chr6:116227733
|
C | T | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+4602C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227733 | ||||||
| chr6:116227781
|
G | C | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.802+4650G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227781 | ||||||
| chr6:116227866
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(96): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.802+4735A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227866 | ||||||
| chr6:116227945
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(78): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+4814G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227945 | ||||||
| chr6:116227948
|
G | A | 16 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+4817G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116227948 | ||||||
| chr6:116228118
|
A | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.802+4987A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228118 | ||||||
| chr6:116228228
|
G | T | 1 | a0001c0001t0006g0009 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.802+5097G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228228 | ||||||
| chr6:116228279
|
CG | C | 7 | a0001c0001t0006g0161a0001c0001t0007g0129a0001c0001t0007g0130others(4): Show | 7 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+5150delG | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116228279 | |||||
| chr6:116228341
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.802+5210T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228341 | ||||||
| chr6:116228368
|
C | A | 1 | a0001c0001t0004g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.802+5237C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228368 | ||||||
| chr6:116228411
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0033g0281 | 3 | HG00642.hp1 HG03130.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.802+5280G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228411 | ||||||
| chr6:116228452
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.802+5321G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228452 | ||||||
| chr6:116228508
|
CA | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(260): Show | 268 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.802+5388delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116228508 | |||||
| chr6:116228619
|
G | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(78): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+5488G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228619 | ||||||
| chr6:116228764
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0205 | 2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.802+5633A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228764 | ||||||
| chr6:116228801
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.802+5670C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228801 | ||||||
| chr6:116228968
|
G | A | 1 | a0001c0001t0028g0027 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.802+5837G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116228968 | ||||||
| chr6:116229010
|
G | A | 2 | a0001c0001t0003g0233a0001c0001t0004g0040 | 2 | HG02132.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.802+5879G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229010 | ||||||
| chr6:116229063
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.802+5932G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229063 | ||||||
| chr6:116229169
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.802+6038A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229169 | ||||||
| chr6:116229283
|
C | T | 2 | a0001c0001t0004g0257a0001c0001t0008g0258 | 2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.802+6152C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229283 | ||||||
| chr6:116229490
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.802+6359G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229490 | ||||||
| chr6:116229533
|
G | A | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.802+6402G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229533 | ||||||
| chr6:116229754
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(262): Show | 270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.802+6623A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229754 | ||||||
| chr6:116229807
|
G | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+6676G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229807 | ||||||
| chr6:116229904
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(78): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.802+6773C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229904 | ||||||
| chr6:116229970
|
C | G | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+6839C>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116229970 | ||||||
| chr6:116230320
|
C | A | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG01993.hp1 HG02300.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-6646C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230320 | ||||||
| chr6:116230440
|
C | T | 1 | a0001c0001t0003g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.803-6526C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230440 | ||||||
| chr6:116230458
|
A | C | 3 | a0001c0001t0010g0102a0001c0001t0010g0103a0001c0001t0010g0104 | 3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.803-6508A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230458 | ||||||
| chr6:116230475
|
C | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(260): Show | 268 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.803-6491C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230475 | ||||||
| chr6:116230836
|
G | A | 1 | a0001c0001t0014g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.803-6130G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230836 | ||||||
| chr6:116230914
|
A | G | 4 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0052others(1): Show | 4 | NA18971.hp2 NA18978.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-6052A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230914 | ||||||
| chr6:116230940
|
C | T | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-6026C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230940 | ||||||
| chr6:116230975
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.803-5991C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116230975 | ||||||
| chr6:116231106
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(91): Show | 96 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.803-5840dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | |||||
| chr6:116231106
|
CA | C | 138 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(135): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.803-5840delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | |||||
| chr6:116231106
|
CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-5850_803-5840d others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231106 | |||||
| chr6:116231148
|
T | TC | 106 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(103): Show | 108 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.803-5809dupC | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | |||||
| chr6:116231148
|
T | TCC | 101 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(98): Show | 102 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.803-5810_803-5809d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | |||||
| chr6:116231148
|
T | TCCC | 45 | a0001c0001t0002g0047a0001c0001t0002g0265a0001c0001t0002g0267others(42): Show | 47 | HG00408.hp2 HG00558.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.803-5811_803-5809d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116231148 | |||||
| chr6:116231395
|
A | G | 2 | a0001c0001t0007g0270a0001c0001t0007g0271 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.803-5571A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231395 | ||||||
| chr6:116231588
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.803-5378T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231588 | ||||||
| chr6:116231705
|
G | A | 6 | a0001c0001t0003g0049a0001c0001t0004g0050a0001c0001t0005g0095others(3): Show | 6 | HG01106.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-5261G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231705 | ||||||
| chr6:116231824
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-5142T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231824 | ||||||
| chr6:116231872
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.803-5094G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231872 | ||||||
| chr6:116231903
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(96): Show | 101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.803-5063G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231903 | ||||||
| chr6:116231933
|
G | T | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.803-5033G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231933 | ||||||
| chr6:116231971
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-4995C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116231971 | ||||||
| chr6:116232159
|
C | CTG | 265 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(262): Show | 270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.803-4806_803-4805i others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116232159 | |||||
| chr6:116232161
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.803-4805A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232161 | ||||||
| chr6:116232188
|
C | T | 8 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-4778C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232188 | ||||||
| chr6:116232286
|
A | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0162a0001c0001t0001g0224others(3): Show | 6 | HG01192.hp2 HG01243.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4680A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232286 | ||||||
| chr6:116232348
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.803-4618A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232348 | ||||||
| chr6:116232405
|
A | C | 1 | a0001c0001t0038g0141 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.803-4561A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232405 | ||||||
| chr6:116232411
|
T | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-4555T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232411 | ||||||
| chr6:116232525
|
GA | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-4434delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116232525 | |||||
| chr6:116232554
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.803-4412A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232554 | ||||||
| chr6:116232937
|
C | T | 1 | a0001c0001t0023g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-4029C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116232937 | ||||||
| chr6:116233019
|
T | C | 34 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(31): Show | 36 | HG00408.hp2 HG00558.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.803-3947T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233019 | ||||||
| chr6:116233182
|
A | T | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803-3784A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233182 | ||||||
| chr6:116233298
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.803-3668T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233298 | ||||||
| chr6:116233550
|
G | A | 4 | a0001c0001t0012g0169a0001c0001t0012g0170a0001c0001t0012g0171others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-3416G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233550 | ||||||
| chr6:116233625
|
A | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-3341A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233625 | ||||||
| chr6:116233916
|
C | T | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.803-3050C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116233916 | ||||||
| chr6:116233977
|
G | GT | 116 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(113): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.803-2971dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | |||||
| chr6:116233977
|
G | GTT | 107 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0226others(104): Show | 109 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.803-2972_803-2971d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | |||||
| chr6:116233977
|
GT | G | 14 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-2971delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116233977 | |||||
| chr6:116234012
|
C | T | 1 | a0001c0001t0017g0294 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.803-2954C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234012 | ||||||
| chr6:116234195
|
C | T | 1 | a0001c0001t0018g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.803-2771C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234195 | ||||||
| chr6:116234457
|
A | G | 2 | a0001c0001t0010g0100a0001c0001t0010g0101 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.803-2509A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234457 | ||||||
| chr6:116234715
|
T | C | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-2251T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234715 | ||||||
| chr6:116234813
|
C | T | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG01993.hp1 HG02300.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2153C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234813 | ||||||
| chr6:116234821
|
C | T | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-2145C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116234821 | ||||||
| chr6:116235035
|
GT | G | 12 | a0001c0001t0001g0094a0001c0001t0003g0032a0001c0001t0003g0288others(9): Show | 12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-1913delT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | |||||
| chr6:116235035
|
GTT | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(242): Show | 250 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.803-1914_803-1913d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | |||||
| chr6:116235035
|
GTTT | G | 8 | a0001c0001t0002g0265a0001c0001t0008g0258a0001c0001t0017g0059others(5): Show | 8 | HG02280.hp1 HG02630.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1915_803-1913d others(5): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235035 | |||||
| chr6:116235252
|
G | T | 2 | a0001c0001t0017g0059a0001c0001t0017g0294 | 2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.803-1714G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235252 | ||||||
| chr6:116235279
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.803-1687G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235279 | ||||||
| chr6:116235328
|
A | G | 21 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(18): Show | 21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-1638A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235328 | ||||||
| chr6:116235455
|
A | T | 1 | a0001c0001t0001g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.803-1511A>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235455 | ||||||
| chr6:116235731
|
T | C | 1 | a0001c0003t0014g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-1235T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235731 | ||||||
| chr6:116235835
|
A | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.803-1131A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116235835 | ||||||
| chr6:116235900
|
A | AGCCAATG | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-1065_803-1059d others(9): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr6 | 116235900 | |||||
| chr6:116236091
|
G | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0205 | 2 | HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.803-875G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236091 | ||||||
| chr6:116236159
|
A | G | 2 | a0001c0001t0007g0270a0001c0001t0007g0271 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.803-807A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236159 | ||||||
| chr6:116236498
|
G | C | 16 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(13): Show | 17 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-468G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236498 | ||||||
| chr6:116236786
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.803-180G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 8/11 | chr6 | 116236786 | ||||||
| chr6:116237408
|
G | T | 2 | a0001c0001t0014g0247a0001c0001t0018g0276 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.921+324G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237408 | ||||||
| chr6:116237445
|
C | A | 1 | a0001c0001t0003g0024 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.921+361C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237445 | ||||||
| chr6:116237576
|
G | A | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+492G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237576 | ||||||
| chr6:116237622
|
A | G | 8 | a0001c0001t0010g0100a0001c0001t0010g0101a0001c0001t0010g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+538A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237622 | ||||||
| chr6:116237773
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.922-414A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237773 | ||||||
| chr6:116237799
|
A | G | 23 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(20): Show | 23 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.922-388A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116237799 | ||||||
| chr6:116238161
|
A | G | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.922-26A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 9/11 | chr6 | 116238161 | ||||||
| chr6:116238409
|
A | G | 1 | a0001c0001t0007g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1083+61A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | chr6 | 116238409 | ||||||
| chr6:116238464
|
TA | T | 96 | a0001c0001t0001g0145a0001c0001t0001g0185a0001c0001t0001g0208others(93): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1083+136delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | |||||
| chr6:116238464
|
TAA | T | 33 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(30): Show | 33 | HG00639.hp1 HG01074.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1083+135_1083+136d others(4): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | |||||
| chr6:116238464
|
TAAAAAAA others(2): Show |
T | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1083+128_1083+136d others(11): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr6 | 116238464 | |||||
| chr6:116238862
|
G | C | 115 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(112): Show | 117 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1084-93G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 10/11 | chr6 | 116238862 | ||||||
| chr6:116239168
|
T | A | 15 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(12): Show | 15 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1252+45T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239168 | ||||||
| chr6:116239255
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1252+132T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239255 | ||||||
| chr6:116239260
|
C | A | 1 | a0001c0001t0005g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1252+137C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239260 | ||||||
| chr6:116239558
|
C | T | 25 | a0001c0001t0006g0005a0001c0001t0006g0009a0001c0001t0006g0010others(22): Show | 26 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1252+435C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239558 | ||||||
| chr6:116239603
|
G | A | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1252+480G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239603 | ||||||
| chr6:116239645
|
G | C | 3 | a0001c0001t0016g0116a0001c0001t0016g0117a0001c0001t0025g0115 | 3 | HG01891.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1252+522G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239645 | ||||||
| chr6:116239707
|
C | T | 1 | a0001c0001t0008g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1252+584C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239707 | ||||||
| chr6:116239708
|
A | G | 139 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1252+585A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239708 | ||||||
| chr6:116239904
|
T | G | 1 | a0001c0001t0002g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1252+781T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239904 | ||||||
| chr6:116239924
|
T | C | 25 | a0001c0001t0003g0288a0001c0001t0004g0155a0001c0001t0004g0157others(22): Show | 25 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1252+801T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116239924 | ||||||
| chr6:116240015
|
G | A | 1 | a0001c0001t0010g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1252+892G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240015 | ||||||
| chr6:116240158
|
G | C | 1 | a0001c0001t0002g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1252+1035G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240158 | ||||||
| chr6:116240548
|
T | A | 73 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(70): Show | 75 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1252+1425T>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240548 | ||||||
| chr6:116240646
|
T | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | NA18971.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1252+1523T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240646 | ||||||
| chr6:116240751
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1252+1628G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240751 | ||||||
| chr6:116240841
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0038g0141 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1252+1718A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240841 | ||||||
| chr6:116240901
|
T | G | 2 | a0001c0001t0007g0270a0001c0001t0007g0271 | 2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1252+1778T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116240901 | ||||||
| chr6:116241010
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(260): Show | 268 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1252+1887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241010 | ||||||
| chr6:116241141
|
C | CA | 28 | a0001c0001t0001g0209a0001c0001t0002g0051a0001c0001t0002g0241others(25): Show | 29 | HG00642.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1252+2036dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241141 | |||||
| chr6:116241141
|
CA | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1252+2036delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241141 | |||||
| chr6:116241478
|
G | T | 1 | a0001c0001t0008g0008 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1252+2355G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241478 | ||||||
| chr6:116241593
|
A | C | 1 | a0001c0001t0005g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1253-2316A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241593 | ||||||
| chr6:116241751
|
G | A | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1253-2158G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241751 | ||||||
| chr6:116241792
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0221 | 2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1253-2117G>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241792 | ||||||
| chr6:116241855
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0180 | 2 | HG02071.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1253-2054G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241855 | ||||||
| chr6:116241918
|
G | A | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1253-1991G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241918 | ||||||
| chr6:116241921
|
TCAAAAAA others(15): Show |
T | 40 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(37): Show | 40 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1253-1971_1253-195 others(26): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241921 | |||||
| chr6:116241922
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0002g0265 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1253-1972_1253-195 others(27): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241922 | |||||
| chr6:116241923
|
AAAAAAAA others(14): Show |
A | 75 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0007others(72): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1253-1966_1253-194 others(25): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241923 | |||||
| chr6:116241924
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0005g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1253-1970_1253-195 others(24): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241924 | |||||
| chr6:116241929
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0180a0001c0001t0011g0090 | 2 | HG01169.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(19): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241929 | |||||
| chr6:116241930
|
AAAAAAAA others(7): Show |
A | 82 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(79): Show | 84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(18): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241930 | |||||
| chr6:116241931
|
AAAAAAAA others(6): Show |
A | 15 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0151others(12): Show | 15 | HG00738.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1253-1970_1253-195 others(17): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241931 | |||||
| chr6:116241933
|
AAAAAACA others(4): Show |
A | 16 | a0001c0001t0002g0047a0001c0001t0002g0098a0001c0001t0002g0240others(13): Show | 16 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(15): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241933 | |||||
| chr6:116241934
|
AAAAACAA others(3): Show |
A | 6 | a0001c0001t0002g0053a0001c0001t0002g0241a0001c0001t0002g0264others(3): Show | 6 | HG03098.hp1 HG03130.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(14): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241934 | |||||
| chr6:116241935
|
AAAACAAA others(2): Show |
A | 17 | a0001c0001t0002g0239a0001c0001t0006g0005a0001c0001t0006g0009others(14): Show | 18 | HG00642.hp2 HG01106.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(13): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241935 | |||||
| chr6:116241936
|
AAACAAAA others(1): Show |
A | 9 | a0001c0001t0006g0052a0001c0001t0006g0058a0001c0001t0006g0161others(6): Show | 9 | HG01123.hp2 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253-1970_1253-196 others(12): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241936 | |||||
| chr6:116241944
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1253-1965C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241944 | ||||||
| chr6:116241944
|
CA | C | 13 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0076others(10): Show | 13 | HG00642.hp1 HG00738.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1253-1950delA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116241944 | |||||
| chr6:116241988
|
A | C | 1 | a0001c0001t0033g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1253-1921A>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116241988 | ||||||
| chr6:116242100
|
A | G | 164 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0054others(161): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1253-1809A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242100 | ||||||
| chr6:116242380
|
T | G | 3 | a0001c0001t0005g0134a0001c0001t0005g0139a0001c0001t0005g0262 | 3 | HG03239.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1253-1529T>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242380 | ||||||
| chr6:116242384
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(260): Show | 268 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1253-1525A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242384 | ||||||
| chr6:116242401
|
A | G | 2 | a0001c0001t0020g0232a0001c0001t0020g0238 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1253-1508A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242401 | ||||||
| chr6:116242482
|
C | CA | 14 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0124others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1253-1414dupA | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116242482 | |||||
| chr6:116242494
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1253-1415A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242494 | ||||||
| chr6:116242604
|
C | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(262): Show | 270 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1253-1305C>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242604 | ||||||
| chr6:116242662
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(263): Show | 271 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1253-1247T>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242662 | ||||||
| chr6:116242762
|
G | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(263): Show | 271 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1253-1147G>C | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242762 | ||||||
| chr6:116242808
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1253-1101C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242808 | ||||||
| chr6:116242948
|
A | G | 4 | a0001c0001t0011g0090a0001c0001t0011g0091a0001c0001t0011g0213others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1253-961A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116242948 | ||||||
| chr6:116243022
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1253-887A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243022 | ||||||
| chr6:116243050
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1253-859G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243050 | ||||||
| chr6:116243065
|
C | T | 12 | a0001c0001t0009g0107a0001c0001t0009g0108a0001c0001t0009g0109others(9): Show | 12 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1253-844C>T | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243065 | ||||||
| chr6:116243066
|
G | A | 1 | a0001c0001t0011g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1253-843G>A | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243066 | ||||||
| chr6:116243225
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0043others(257): Show | 265 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1253-684A>G | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243225 | ||||||
| chr6:116243437
|
A | AT | 21 | a0001c0001t0002g0047a0001c0001t0002g0053a0001c0001t0002g0098others(18): Show | 21 | HG01099.hp2 HG01515.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.1253-470dupT | NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr6 | 116243437 | |||||
| chr6:116243839
|
CAA | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0234a0001c0001t0001g0235 | 5 | NA18972.hp2 NA18973.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.1253-69_1253-68del others(2): Show |
NT5DC1 | ENSG00000178425.14 | transcript | ENST00000319550.9 | protein_coding | 11/11 | chr6 | 116243839 |