Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9348 |
|---|---|
| ensemblid | ENSG00000164100.9 |
| hgncid | 7682 |
| symbol | NDST3 |
| name | N-deacetylase and N-sulfotransferase 3 |
| refseq_nuc | NM_004784.3 |
| refseq_prot | NP_004775.1 |
| ensembl_nuc | ENST00000296499.6 |
| ensembl_prot | ENSP00000296499.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 118034486 |
| end | 118258634 |
| strand | + |
| ver | v1.2 |
| region | chr4:118034486-118258634 |
| region5000 | chr4:118029486-118263634 |
| regionname0 | NDST3_chr4_118034486_118258634 |
| regionname5000 | NDST3_chr4_118029486_118263634 |
| 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 | 873 | 216 | 62 | 38 | 92 | 2 | 20 | 76 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| 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 | 2622 | 112 | 22 | 15 | 69 | 1 | 3 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0002 | 0/0 | 2622 | 39 | 8 | 6 | 16 | 1 | 8 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0003 | 0/0 | 2622 | 29 | 3 | 13 | 6 | 0 | 7 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0004 | 0/0 | 2622 | 9 | 9 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0005 | 0/0 | 2622 | 5 | 5 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0006 | 0/0 | 2622 | 4 | 4 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0007 | 0/0 | 2622 | 4 | 3 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0008 | 0/0 | 2622 | 2 | 1 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0009 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0010 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0011 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0012 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0013 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0014 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0015 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0016 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0017 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| c0018 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| 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 | 1/1 | 3185 | 155 | 39 | 22 | 80 | 2 | 10 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0002 | 0/0 | 3185 | 29 | 4 | 13 | 7 | 0 | 5 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0003 | 0/0 | 3184 | 11 | 8 | 2 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0004 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0005 | 0/0 | 3185 | 2 | 1 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0006 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0007 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0008 | 0/0 | 3226 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0009 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0010 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0011 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0012 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0013 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0014 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0015 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0016 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0017 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0018 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0019 | 0/0 | 3184 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0020 | 0/0 | 3184 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| t0021 | 0/0 | 3184 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| 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 | 2622 | 112 | 22 | 15 | 69 | 1 | 3 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0002 | 0/0 | 2622 | 39 | 8 | 6 | 16 | 1 | 8 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0003 | 0/0 | 2622 | 29 | 3 | 13 | 6 | 0 | 7 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0004 | 0/0 | 2622 | 9 | 9 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0005 | 0/0 | 2622 | 5 | 5 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0006 | 0/0 | 2622 | 4 | 4 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0007 | 0/0 | 2622 | 4 | 3 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0008 | 0/0 | 2622 | 2 | 1 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0009 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0010 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0011 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0012 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0013 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0014 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0015 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0016 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0017 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0018 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5806 | 102 | 18 | 15 | 64 | 1 | 2 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0008 | 0/0 | 5847 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0010 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0012 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0013 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0014 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0015 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0016 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0017 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0018 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0001t0020 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0002t0001 | 0/0 | 5806 | 39 | 8 | 6 | 16 | 1 | 8 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0003t0002 | 0/0 | 5806 | 27 | 3 | 13 | 6 | 0 | 5 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0003t0006 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0003t0007 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0004t0001 | 0/0 | 5806 | 4 | 4 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0004t0002 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0004t0003 | 0/0 | 5805 | 3 | 3 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0004t0019 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0005t0001 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0005t0004 | 0/0 | 5806 | 3 | 3 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0006t0001 | 0/0 | 5806 | 3 | 3 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0006t0011 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0007t0001 | 0/0 | 5806 | 4 | 3 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0008t0003 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0008t0005 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0009t0003 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0009t0021 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0010t0003 | 0/0 | 5805 | 2 | 2 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0011t0009 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0012t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0013t0003 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0014t0003 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0015t0005 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0016t0003 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0017t0001 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| a0001c0018t0003 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | copy fasta | chr4 | 118029486 | 118263634 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0015g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0016g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0017g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0018g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0003t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0004t0019g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0005t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0005t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0005t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0006t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0006t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0007t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0008t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0008t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0009t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0009t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0010t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0010t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0011t0009g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0012t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0013t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0014t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0015t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0016t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0017t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| a0001c0018t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0083 | EUR | GBR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0188 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0189 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0074 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01074 | hp2 | a0001 | c0015 | t0005 | g0015 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01109 | hp2 | a0001 | c0016 | t0003 | g0215 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0190 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01243 | hp1 | a0001 | c0007 | t0001 | g0201 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0013 | AMR | PUR | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0209 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0018 | AMR | CLM | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0198 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0010 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0063 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02004 | hp2 | a0001 | c0003 | t0002 | g0034 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | KHV | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0020 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02148 | hp2 | a0001 | c0014 | t0003 | g0021 | AMR | PEL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02258 | hp2 | a0001 | c0008 | t0005 | g0177 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0200 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02451 | hp2 | a0001 | c0010 | t0003 | g0171 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0197 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02602 | hp1 | a0001 | c0003 | t0006 | g0023 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02615 | hp1 | a0001 | c0005 | t0004 | g0100 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0113 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0066 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0115 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02738 | hp2 | a0001 | c0003 | t0007 | g0017 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02809 | hp2 | a0001 | c0013 | t0003 | g0105 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02896 | hp2 | a0001 | c0009 | t0021 | g0067 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02922 | hp2 | a0001 | c0018 | t0003 | g0071 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02976 | hp1 | a0001 | c0004 | t0019 | g0195 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0007 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03041 | hp1 | a0001 | c0005 | t0004 | g0106 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03041 | hp2 | a0001 | c0001 | t0013 | g0119 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0162 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03130 | hp2 | a0001 | c0007 | t0001 | g0203 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0107 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03195 | hp1 | a0001 | c0005 | t0004 | g0108 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0204 | AFR | ESN | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0206 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0183 | SAS | PJL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03486 | hp1 | a0001 | c0017 | t0001 | g0207 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03486 | hp2 | a0001 | c0004 | t0003 | g0194 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0104 | AFR | GWD | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0103 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03579 | hp2 | a0001 | c0009 | t0003 | g0065 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | STU | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0062 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03942 | hp2 | a0001 | c0011 | t0009 | g0053 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0019 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0208 | SAS | STU | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG04204 | hp2 | a0001 | c0008 | t0003 | g0210 | SAS | STU | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | CHB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | CHB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18906 | hp2 | a0001 | c0006 | t0011 | g0102 | AFR | YRI | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18946 | hp2 | a0001 | c0001 | t0015 | g0049 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18947 | hp2 | a0001 | c0001 | t0014 | g0110 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18948 | hp2 | a0001 | c0001 | t0017 | g0036 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18957 | hp1 | a0001 | c0001 | t0010 | g0040 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18960 | hp1 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18973 | hp2 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19007 | hp1 | a0001 | c0012 | t0002 | g0027 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19030 | hp1 | a0001 | c0010 | t0003 | g0213 | AFR | LWK | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | LWK | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20129 | hp2 | a0001 | c0004 | t0003 | g0205 | AFR | ASW | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0016 | SAS | GIH | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | GIH | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0196 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0152 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | USA | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| NA21309 | hp2 | a0001 | c0005 | t0001 | g0109 | AFR | LWK | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0147 | REF | REF | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | NDST3_chr4_118029486_118263634 | NDST3 | chr4 | 118029486 | 118263634 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:118053928
|
G | A | 1 | a0001c0011 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.18G>A | p.Lys6Lys | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/14 | 280/5806 | 18/2622 | 6/873 | chr4 | 118053928 | ||
| chr4:118053991
|
C | T | 3 | a0001c0002a0001c0009a0001c0010 | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
synonymous_variant | LOW | c.81C>T | p.Ile27Ile | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/14 | 343/5806 | 81/2622 | 27/873 | chr4 | 118053991 | ||
| chr4:118054087
|
A | G | 5 | a0001c0004a0001c0007a0001c0016others(2): Show | 16 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(13): Show |
synonymous_variant | LOW | c.177A>G | p.Pro59Pro | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/14 | 439/5806 | 177/2622 | 59/873 | chr4 | 118054087 | ||
| chr4:118054495
|
T | C | 1 | a0001c0012 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.585T>C | p.Ile195Ile | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/14 | 847/5806 | 585/2622 | 195/873 | chr4 | 118054495 | ||
| chr4:118138134
|
T | C | 6 | a0001c0006a0001c0007a0001c0009others(3): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
synonymous_variant | LOW | c.1305T>C | p.Tyr435Tyr | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/14 | 1567/5806 | 1305/2622 | 435/873 | chr4 | 118138134 | ||
| chr4:118224523
|
T | C | 2 | a0001c0005a0001c0017 | 6 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.1572T>C | p.Tyr524Tyr | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/14 | 1834/5806 | 1572/2622 | 524/873 | chr4 | 118224523 | ||
| chr4:118224529
|
T | C | 1 | a0001c0013 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1578T>C | p.Asn526Asn | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/14 | 1840/5806 | 1578/2622 | 526/873 | chr4 | 118224529 | ||
| chr4:118233046
|
T | C | 1 | a0001c0008 | 2 | HG02258.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.1854T>C | p.His618His | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/14 | 2116/5806 | 1854/2622 | 618/873 | chr4 | 118233046 | ||
| chr4:118237190
|
C | T | 1 | a0001c0015 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.2088C>T | p.Asp696Asp | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/14 | 2350/5806 | 2088/2622 | 696/873 | chr4 | 118237190 | ||
| chr4:118240544
|
C | T | 6 | a0001c0009a0001c0010a0001c0013others(3): Show | 8 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
synonymous_variant | LOW | c.2139C>T | p.Asp713Asp | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/14 | 2401/5806 | 2139/2622 | 713/873 | chr4 | 118240544 | ||
| chr4:118240640
|
G | A | 2 | a0001c0003a0001c0012 | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
synonymous_variant | LOW | c.2235G>A | p.Pro745Pro | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/14 | 2497/5806 | 2235/2622 | 745/873 | chr4 | 118240640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:118053910
|
C | G | 1 | a0001c0005t0004 | 3 | HG02615.hp1 HG03041.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-1C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/14 | 1 | chr4 | 118053910 | |||||
| chr4:118255844
|
T | G | 1 | a0001c0003t0006 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 132 | chr4 | 118255844 | |||||
| chr4:118255849
|
C | T | 11 | a0001c0001t0020a0001c0004t0003a0001c0004t0019others(8): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 137 | chr4 | 118255849 | |||||
| chr4:118256095
|
C | T | 1 | a0001c0001t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 383 | chr4 | 118256095 | |||||
| chr4:118256576
|
A | C | 1 | a0001c0001t0017 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*864A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 864 | chr4 | 118256576 | |||||
| chr4:118256582
|
C | G | 1 | a0001c0001t0016 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 870 | chr4 | 118256582 | |||||
| chr4:118256814
|
T | C | 11 | a0001c0001t0020a0001c0004t0003a0001c0004t0019others(8): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1102T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1102 | chr4 | 118256814 | |||||
| chr4:118256917
|
G | A | 7 | a0001c0003t0002a0001c0003t0006a0001c0003t0007others(4): Show | 33 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1205G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1205 | chr4 | 118256917 | |||||
| chr4:118257012
|
A | ACAAAGAT others(34): Show |
1 | a0001c0001t0008 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1304_*1344dupAGAT others(37): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1345 | INFO_REALIGN_3_PRIME | chr4 | 118257012 | ||||
| chr4:118257139
|
AT | A | 11 | a0001c0001t0020a0001c0004t0003a0001c0004t0019others(8): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1438delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1438 | INFO_REALIGN_3_PRIME | chr4 | 118257139 | ||||
| chr4:118257188
|
G | C | 1 | a0001c0004t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1476G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1476 | chr4 | 118257188 | |||||
| chr4:118257378
|
C | A | 1 | a0001c0011t0009 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1666 | chr4 | 118257378 | |||||
| chr4:118257511
|
C | A | 1 | a0001c0004t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1799 | chr4 | 118257511 | |||||
| chr4:118257684
|
A | C | 2 | a0001c0008t0005a0001c0015t0005 | 2 | HG01074.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1972A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 1972 | chr4 | 118257684 | |||||
| chr4:118257722
|
T | C | 1 | a0001c0001t0010 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2010T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2010 | chr4 | 118257722 | |||||
| chr4:118257754
|
A | G | 1 | a0001c0001t0015 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2042 | chr4 | 118257754 | |||||
| chr4:118257806
|
A | T | 10 | a0001c0004t0003a0001c0004t0019a0001c0008t0003others(7): Show | 13 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2094A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2094 | chr4 | 118257806 | |||||
| chr4:118257940
|
A | T | 11 | a0001c0001t0020a0001c0004t0003a0001c0004t0019others(8): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2228A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2228 | chr4 | 118257940 | |||||
| chr4:118258101
|
G | A | 1 | a0001c0006t0011 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2389G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2389 | chr4 | 118258101 | |||||
| chr4:118258109
|
T | C | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2397T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2397 | chr4 | 118258109 | |||||
| chr4:118258263
|
A | G | 1 | a0001c0001t0014 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2551A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2551 | chr4 | 118258263 | |||||
| chr4:118258286
|
A | G | 1 | a0001c0003t0007 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2574A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2574 | chr4 | 118258286 | |||||
| chr4:118258347
|
A | G | 1 | a0001c0009t0021 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2635A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2635 | chr4 | 118258347 | |||||
| chr4:118258413
|
T | A | 11 | a0001c0001t0020a0001c0004t0003a0001c0004t0019others(8): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2701T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2701 | chr4 | 118258413 | |||||
| chr4:118258471
|
G | A | 1 | a0001c0001t0013 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2759G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 14/14 | 2759 | chr4 | 118258471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:118034996
|
A | G | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-156+404A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118034996 | ||||||
| chr4:118035429
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-156+837C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118035429 | ||||||
| chr4:118035439
|
G | GT | 20 | a0001c0001t0001g0212a0001c0002t0001g0211a0001c0003t0002g0208others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.-156+859dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118035439 | |||||
| chr4:118035439
|
GT | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 108 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-156+859delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118035439 | |||||
| chr4:118035952
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-156+1360T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118035952 | ||||||
| chr4:118036294
|
G | T | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-156+1702G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118036294 | ||||||
| chr4:118036612
|
C | A | 15 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-156+2020C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118036612 | ||||||
| chr4:118036745
|
T | G | 20 | a0001c0002t0001g0211a0001c0003t0002g0208a0001c0003t0002g0209others(17): Show | 20 | HG01109.hp2 HG01243.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.-156+2153T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118036745 | ||||||
| chr4:118036988
|
A | AT | 76 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0127others(73): Show | 77 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-156+2406dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118036988 | |||||
| chr4:118037190
|
C | T | 3 | a0001c0005t0001g0107a0001c0005t0004g0106a0001c0005t0004g0108 | 3 | HG03041.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-156+2598C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037190 | ||||||
| chr4:118037275
|
A | C | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156+2683A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037275 | ||||||
| chr4:118037308
|
T | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-156+2716T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037308 | ||||||
| chr4:118037434
|
C | G | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-156+2842C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037434 | ||||||
| chr4:118037609
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG01175.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-156+3017C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037609 | ||||||
| chr4:118037638
|
T | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(21): Show | 24 | HG00544.hp2 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-156+3046T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037638 | ||||||
| chr4:118037988
|
G | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-156+3396G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118037988 | ||||||
| chr4:118038014
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-156+3422G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038014 | ||||||
| chr4:118038221
|
C | A | 4 | a0001c0001t0016g0028a0001c0003t0002g0208a0001c0003t0002g0209others(1): Show | 4 | HG01361.hp1 HG04204.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+3629C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038221 | ||||||
| chr4:118038448
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-156+3856C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038448 | ||||||
| chr4:118038543
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-156+3951C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038543 | ||||||
| chr4:118038679
|
CCCA | C | 4 | a0001c0001t0001g0024a0001c0003t0002g0025a0001c0003t0002g0026others(1): Show | 4 | HG02602.hp1 NA19004.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+4089_-156+409 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118038679 | |||||
| chr4:118038710
|
G | C | 1 | a0001c0002t0001g0029 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-156+4118G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038710 | ||||||
| chr4:118038730
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG00558.hp2 NA18984.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-156+4138T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038730 | ||||||
| chr4:118038987
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+4395G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118038987 | ||||||
| chr4:118039272
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+4680A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118039272 | ||||||
| chr4:118039386
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-156+4794A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118039386 | ||||||
| chr4:118039479
|
A | G | 3 | a0001c0003t0002g0208a0001c0003t0002g0209a0001c0008t0003g0210 | 3 | HG01361.hp1 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-156+4887A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118039479 | ||||||
| chr4:118039691
|
G | C | 1 | a0001c0001t0001g0003 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-156+5099G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118039691 | ||||||
| chr4:118039788
|
A | G | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-156+5196A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118039788 | ||||||
| chr4:118040062
|
G | A | 3 | a0001c0003t0002g0208a0001c0003t0002g0209a0001c0008t0003g0210 | 3 | HG01361.hp1 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-156+5470G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118040062 | ||||||
| chr4:118040387
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-156+5795G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118040387 | ||||||
| chr4:118040770
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-156+6178C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118040770 | ||||||
| chr4:118040845
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-156+6273_-156+629 others(30): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040845 | |||||
| chr4:118040857
|
TTATATAT others(11): Show |
T | 62 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-156+6275_-156+629 others(22): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040857 | |||||
| chr4:118040863
|
ATT | A | 39 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(36): Show | 39 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-156+6275_-156+627 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040863 | |||||
| chr4:118040865
|
T | TTATATAT others(23): Show |
1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-156+6274_-156+627 others(34): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040865 | |||||
| chr4:118040867
|
T | A | 3 | a0001c0001t0001g0126a0001c0001t0020g0113a0001c0002t0001g0211 | 3 | HG02630.hp2 HG03098.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-156+6275T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118040867 | ||||||
| chr4:118040867
|
TTA | T | 3 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0013t0003g0105 | 3 | HG02809.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-156+6289_-156+629 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040867 | |||||
| chr4:118040869
|
A | ATATATAT others(23): Show |
1 | a0001c0005t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-156+6290_-156+631 others(34): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118040869 | |||||
| chr4:118040885
|
A | T | 1 | a0001c0008t0003g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-156+6293A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118040885 | ||||||
| chr4:118041011
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-156+6419G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041011 | ||||||
| chr4:118041251
|
C | T | 8 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(5): Show | 8 | HG02615.hp1 HG02809.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156+6659C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041251 | ||||||
| chr4:118041520
|
A | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-156+6928A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041520 | ||||||
| chr4:118041522
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-156+6930T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041522 | ||||||
| chr4:118041563
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-156+6971G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041563 | ||||||
| chr4:118041930
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-156+7338A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118041930 | ||||||
| chr4:118042218
|
A | G | 1 | a0001c0003t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-156+7626A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118042218 | ||||||
| chr4:118042572
|
A | C | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+7980A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118042572 | ||||||
| chr4:118042774
|
C | T | 1 | a0001c0002t0001g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-156+8182C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118042774 | ||||||
| chr4:118042862
|
ATC | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-156+8280_-156+828 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118042862 | |||||
| chr4:118043069
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-156+8477A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043069 | ||||||
| chr4:118043158
|
A | G | 1 | a0001c0003t0002g0022 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-156+8566A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043158 | ||||||
| chr4:118043197
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-156+8605A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043197 | ||||||
| chr4:118043229
|
A | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-156+8637A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043229 | ||||||
| chr4:118043582
|
C | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-156+8990C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043582 | ||||||
| chr4:118043895
|
A | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-156+9303A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118043895 | ||||||
| chr4:118044298
|
C | T | 3 | a0001c0003t0002g0208a0001c0003t0002g0209a0001c0008t0003g0210 | 3 | HG01361.hp1 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-155-9458C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044298 | ||||||
| chr4:118044514
|
C | T | 2 | a0001c0001t0001g0193a0001c0005t0001g0109 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-155-9242C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044514 | ||||||
| chr4:118044547
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-155-9209G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044547 | ||||||
| chr4:118044813
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-8943G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044813 | ||||||
| chr4:118044837
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-155-8919G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044837 | ||||||
| chr4:118044845
|
A | C | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-155-8911A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044845 | ||||||
| chr4:118044866
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG01175.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-155-8890T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118044866 | ||||||
| chr4:118045292
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-155-8464A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118045292 | ||||||
| chr4:118045444
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-155-8312A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118045444 | ||||||
| chr4:118045577
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-155-8179C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118045577 | ||||||
| chr4:118045783
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-155-7973C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118045783 | ||||||
| chr4:118045839
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-155-7917C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118045839 | ||||||
| chr4:118046004
|
A | G | 12 | a0001c0001t0001g0184a0001c0002t0001g0088a0001c0002t0001g0089others(9): Show | 12 | NA18747.hp2 NA18945.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-7752A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046004 | ||||||
| chr4:118046011
|
C | T | 1 | a0001c0001t0008g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-155-7745C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046011 | ||||||
| chr4:118046041
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-155-7715A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046041 | ||||||
| chr4:118046059
|
T | C | 1 | a0001c0008t0003g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-155-7697T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046059 | ||||||
| chr4:118046221
|
C | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-155-7535C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046221 | ||||||
| chr4:118046379
|
G | A | 1 | a0001c0004t0003g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-155-7377G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046379 | ||||||
| chr4:118046381
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-155-7375T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046381 | ||||||
| chr4:118046595
|
C | T | 1 | a0001c0002t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-155-7161C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046595 | ||||||
| chr4:118046612
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-155-7144C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046612 | ||||||
| chr4:118046706
|
G | A | 10 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-155-7050G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118046706 | ||||||
| chr4:118046922
|
A | AC | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-155-6833dupC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118046922 | |||||
| chr4:118047122
|
C | T | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-155-6634C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047122 | ||||||
| chr4:118047136
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-155-6620C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047136 | ||||||
| chr4:118047169
|
T | C | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-155-6587T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047169 | ||||||
| chr4:118047324
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-155-6432G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047324 | ||||||
| chr4:118047495
|
G | A | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-155-6261G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047495 | ||||||
| chr4:118047904
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-155-5852C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047904 | ||||||
| chr4:118047980
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-155-5776A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118047980 | ||||||
| chr4:118048203
|
T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-5553T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048203 | ||||||
| chr4:118048340
|
T | G | 5 | a0001c0001t0016g0028a0001c0003t0002g0034a0001c0003t0002g0035others(2): Show | 5 | HG01975.hp2 HG02004.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-5416T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048340 | ||||||
| chr4:118048684
|
C | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-155-5072C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048684 | ||||||
| chr4:118048729
|
C | A | 17 | a0001c0003t0002g0209a0001c0004t0001g0197a0001c0004t0001g0199others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-5027C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048729 | ||||||
| chr4:118048732
|
A | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-5024A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048732 | ||||||
| chr4:118048917
|
A | G | 1 | a0001c0002t0001g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-155-4839A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048917 | ||||||
| chr4:118048977
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-4779C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118048977 | ||||||
| chr4:118049140
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-4616G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049140 | ||||||
| chr4:118049162
|
T | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-4594T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049162 | ||||||
| chr4:118049438
|
G | A | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-155-4318G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049438 | ||||||
| chr4:118049460
|
C | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-4296C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049460 | ||||||
| chr4:118049480
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(30): Show | 33 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-155-4276A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049480 | ||||||
| chr4:118049662
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-155-4094C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049662 | ||||||
| chr4:118049677
|
T | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-155-4079T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049677 | ||||||
| chr4:118049732
|
TA | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(8): Show | 11 | HG00597.hp1 HG01070.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-155-4012delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 118049732 | |||||
| chr4:118049733
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-155-4023A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049733 | ||||||
| chr4:118049735
|
A | T | 16 | a0001c0002t0001g0211a0001c0004t0001g0197a0001c0004t0001g0199others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-155-4021A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049735 | ||||||
| chr4:118049794
|
G | C | 1 | a0001c0009t0003g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-155-3962G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049794 | ||||||
| chr4:118049842
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-155-3914C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049842 | ||||||
| chr4:118049904
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-155-3852T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049904 | ||||||
| chr4:118049966
|
T | C | 1 | a0001c0012t0002g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-155-3790T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049966 | ||||||
| chr4:118049971
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-3785G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049971 | ||||||
| chr4:118049991
|
A | T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-155-3765A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118049991 | ||||||
| chr4:118050145
|
C | T | 1 | a0001c0003t0002g0180 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-155-3611C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050145 | ||||||
| chr4:118050171
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-155-3585A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050171 | ||||||
| chr4:118050199
|
C | G | 1 | a0001c0002t0001g0178 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-155-3557C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050199 | ||||||
| chr4:118050317
|
G | T | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-155-3439G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050317 | ||||||
| chr4:118050600
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-3156A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050600 | ||||||
| chr4:118050717
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-155-3039A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050717 | ||||||
| chr4:118050788
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-155-2968G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050788 | ||||||
| chr4:118050903
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-155-2853G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050903 | ||||||
| chr4:118050918
|
T | A | 1 | a0001c0003t0002g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-155-2838T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050918 | ||||||
| chr4:118050973
|
C | A | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-155-2783C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118050973 | ||||||
| chr4:118051026
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-2730T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051026 | ||||||
| chr4:118051030
|
C | T | 7 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0081others(4): Show | 7 | HG00099.hp1 HG00735.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-2726C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051030 | ||||||
| chr4:118051146
|
G | A | 15 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-155-2610G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051146 | ||||||
| chr4:118051168
|
A | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-155-2588A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051168 | ||||||
| chr4:118051183
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-155-2573A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051183 | ||||||
| chr4:118051439
|
G | A | 2 | a0001c0003t0002g0209a0001c0008t0003g0210 | 2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-155-2317G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051439 | ||||||
| chr4:118051492
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-155-2264A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051492 | ||||||
| chr4:118051676
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-155-2080T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051676 | ||||||
| chr4:118051852
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-155-1904C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051852 | ||||||
| chr4:118051962
|
G | A | 15 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-155-1794G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118051962 | ||||||
| chr4:118052095
|
C | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-155-1661C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052095 | ||||||
| chr4:118052224
|
C | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-1532C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052224 | ||||||
| chr4:118052286
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-155-1470A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052286 | ||||||
| chr4:118052352
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-1404C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052352 | ||||||
| chr4:118052411
|
C | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-155-1345C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052411 | ||||||
| chr4:118052533
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-155-1223C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052533 | ||||||
| chr4:118052952
|
T | C | 9 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-155-804T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118052952 | ||||||
| chr4:118053391
|
T | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-365T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118053391 | ||||||
| chr4:118053586
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-155-170C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118053586 | ||||||
| chr4:118053634
|
C | T | 15 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-155-122C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118053634 | ||||||
| chr4:118053649
|
C | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-155-107C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118053649 | ||||||
| chr4:118053665
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.-155-91G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 1/13 | chr4 | 118053665 | ||||||
| chr4:118055075
|
A | G | 14 | a0001c0001t0001g0164a0001c0004t0001g0199a0001c0004t0001g0202others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+184A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055075 | ||||||
| chr4:118055097
|
G | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+206G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055097 | ||||||
| chr4:118055163
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.981+272C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055163 | ||||||
| chr4:118055266
|
T | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+375T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055266 | ||||||
| chr4:118055337
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+446A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055337 | ||||||
| chr4:118055434
|
A | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+543A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055434 | ||||||
| chr4:118055465
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+574C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055465 | ||||||
| chr4:118055639
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981+748A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055639 | ||||||
| chr4:118055673
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+782A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118055673 | ||||||
| chr4:118056086
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+1195C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056086 | ||||||
| chr4:118056116
|
T | A | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.981+1225T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056116 | ||||||
| chr4:118056330
|
C | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+1439C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056330 | ||||||
| chr4:118056425
|
T | G | 1 | a0001c0003t0002g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.981+1534T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056425 | ||||||
| chr4:118056442
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+1551G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056442 | ||||||
| chr4:118056466
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+1575A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056466 | ||||||
| chr4:118056533
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+1642T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056533 | ||||||
| chr4:118056786
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+1895A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056786 | ||||||
| chr4:118056821
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.981+1930T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056821 | ||||||
| chr4:118056833
|
A | G | 14 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+1942A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056833 | ||||||
| chr4:118056879
|
G | A | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+1988G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056879 | ||||||
| chr4:118056902
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+2011T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118056902 | ||||||
| chr4:118057611
|
T | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+2720T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118057611 | ||||||
| chr4:118057753
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+2862A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118057753 | ||||||
| chr4:118057943
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.981+3052C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118057943 | ||||||
| chr4:118058087
|
CACTTATG others(4): Show |
C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+3198_981+3208d others(13): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058087 | |||||
| chr4:118058139
|
A | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+3248A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058139 | ||||||
| chr4:118058257
|
A | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.981+3366A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058257 | ||||||
| chr4:118058337
|
T | C | 1 | a0001c0004t0001g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.981+3446T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058337 | ||||||
| chr4:118058349
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+3458A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058349 | ||||||
| chr4:118058430
|
C | CA | 9 | a0001c0001t0001g0130a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG01175.hp2 HG02027.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+3555dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058430 | |||||
| chr4:118058430
|
C | CAAA | 48 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.981+3553_981+3555d others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058430 | |||||
| chr4:118058430
|
CA | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.981+3555delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058430 | |||||
| chr4:118058594
|
A | AGT | 15 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0128others(12): Show | 15 | HG00544.hp1 HG01361.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+3743_981+3744d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058594 | |||||
| chr4:118058594
|
A | AGTGT | 2 | a0001c0001t0001g0125a0001c0001t0001g0127 | 2 | HG02809.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.981+3741_981+3744d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058594 | |||||
| chr4:118058594
|
AGT | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+3743_981+3744d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058594 | |||||
| chr4:118058594
|
AGTGT | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG00558.hp1 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+3741_981+3744d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058594 | |||||
| chr4:118058594
|
AGTGTGT | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+3739_981+3744d others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058594 | |||||
| chr4:118058620
|
TGTGTGTG others(17): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.981+3731_981+3754d others(26): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058620 | |||||
| chr4:118058622
|
TGTGTGTG others(15): Show |
T | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0041others(13): Show | 16 | HG00544.hp2 HG01070.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.981+3733_981+3754d others(24): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058622 | |||||
| chr4:118058624
|
TGTGTGTG others(7): Show |
T | 2 | a0001c0004t0019g0195a0001c0007t0001g0200 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.981+3735_981+3748d others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058624 | |||||
| chr4:118058624
|
TGTGTGTG others(13): Show |
T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0001g0170others(1): Show | 4 | HG02922.hp1 HG03471.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+3735_981+3754d others(22): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058624 | |||||
| chr4:118058626
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0004t0003g0205a0001c0005t0001g0109 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.981+3737_981+3748d others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058626 | |||||
| chr4:118058626
|
TGTGTGTG others(7): Show |
T | 9 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+3737_981+3750d others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058626 | |||||
| chr4:118058626
|
TGTGTGTG others(11): Show |
T | 21 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0038others(18): Show | 21 | HG00099.hp2 HG00735.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.981+3737_981+3754d others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058626 | |||||
| chr4:118058628
|
TGTGTGTG others(1): Show |
T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+3739_981+3746d others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058628 | |||||
| chr4:118058628
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0004t0003g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.981+3739_981+3750d others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058628 | |||||
| chr4:118058628
|
TGTGTGTG others(9): Show |
T | 39 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(36): Show | 39 | HG00558.hp2 HG00639.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+3739_981+3754d others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058628 | |||||
| chr4:118058630
|
TGTGTGCG others(7): Show |
T | 43 | a0001c0001t0001g0024a0001c0001t0001g0184a0001c0001t0020g0113others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.981+3741_981+3754d others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058630 | |||||
| chr4:118058632
|
TGTGCGCG others(5): Show |
T | 6 | a0001c0002t0001g0078a0001c0002t0001g0084a0001c0002t0001g0214others(3): Show | 6 | HG02602.hp2 HG02809.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+3743_981+3754d others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058632 | |||||
| chr4:118058634
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0149others(1): Show | 4 | NA18612.hp1 NA18954.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+3743T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058634 | ||||||
| chr4:118058634
|
TGCGCGCG others(3): Show |
T | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.981+3746_981+3755d others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118058634 | |||||
| chr4:118058785
|
C | A | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+3894C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058785 | ||||||
| chr4:118058886
|
C | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+3995C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058886 | ||||||
| chr4:118058945
|
C | T | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+4054C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118058945 | ||||||
| chr4:118059184
|
A | G | 1 | a0001c0005t0004g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.981+4293A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118059184 | ||||||
| chr4:118059485
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.981+4594G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118059485 | ||||||
| chr4:118059623
|
C | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+4732C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118059623 | ||||||
| chr4:118059647
|
CAGCTAAG others(3): Show |
C | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.981+4760_981+4769d others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118059647 | |||||
| chr4:118059654
|
G | GC | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+4763_981+4764i others(3): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118059654 | ||||||
| chr4:118060255
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.981+5364G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118060255 | ||||||
| chr4:118060604
|
T | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.981+5713T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118060604 | ||||||
| chr4:118060772
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.981+5881A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118060772 | ||||||
| chr4:118060814
|
C | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+5923C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118060814 | ||||||
| chr4:118060925
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.981+6034A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118060925 | ||||||
| chr4:118061076
|
C | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+6185C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061076 | ||||||
| chr4:118061353
|
C | T | 1 | a0001c0006t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.981+6462C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061353 | ||||||
| chr4:118061474
|
T | C | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+6583T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061474 | ||||||
| chr4:118061498
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+6607T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061498 | ||||||
| chr4:118061501
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.981+6610C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061501 | ||||||
| chr4:118061744
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+6853G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061744 | ||||||
| chr4:118061831
|
T | C | 13 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0088others(10): Show | 13 | HG00597.hp1 NA18747.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+6940T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061831 | ||||||
| chr4:118061868
|
G | A | 2 | a0001c0001t0020g0113a0001c0003t0002g0007 | 2 | HG02630.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.981+6977G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118061868 | ||||||
| chr4:118062070
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+7179G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062070 | ||||||
| chr4:118062407
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.981+7516T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062407 | ||||||
| chr4:118062412
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA18956.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.981+7521T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062412 | ||||||
| chr4:118062636
|
A | T | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+7745A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062636 | ||||||
| chr4:118062650
|
C | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+7759C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062650 | ||||||
| chr4:118062674
|
AG | A | 52 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(49): Show | 52 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.981+7786delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118062674 | |||||
| chr4:118062794
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+7903G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118062794 | ||||||
| chr4:118063021
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | NA18941.hp2 NA18946.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+8130T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063021 | ||||||
| chr4:118063057
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+8166G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063057 | ||||||
| chr4:118063186
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+8295G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063186 | ||||||
| chr4:118063189
|
TA | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.981+8315delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118063189 | |||||
| chr4:118063375
|
C | T | 56 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(53): Show | 56 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.981+8484C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063375 | ||||||
| chr4:118063480
|
G | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+8589G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063480 | ||||||
| chr4:118063637
|
A | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.981+8746A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063637 | ||||||
| chr4:118063949
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+9058T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063949 | ||||||
| chr4:118063950
|
G | A | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.981+9059G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118063950 | ||||||
| chr4:118064019
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.981+9128C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064019 | ||||||
| chr4:118064104
|
T | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+9213T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064104 | ||||||
| chr4:118064453
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+9562G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064453 | ||||||
| chr4:118064599
|
T | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+9708T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064599 | ||||||
| chr4:118064728
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+9837C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064728 | ||||||
| chr4:118064795
|
C | T | 13 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0088others(10): Show | 13 | HG00597.hp1 NA18747.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+9904C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118064795 | ||||||
| chr4:118065151
|
G | A | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.981+10260G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118065151 | ||||||
| chr4:118065204
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.981+10313A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118065204 | ||||||
| chr4:118065415
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+10524A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118065415 | ||||||
| chr4:118065853
|
C | T | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.981+10962C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118065853 | ||||||
| chr4:118066082
|
A | ATTATATA others(23): Show |
1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.981+11245_981+1127 others(34): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066082 | |||||
| chr4:118066082
|
ATTATATA others(23): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.981+11245_981+1127 others(34): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066082 | |||||
| chr4:118066120
|
T | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+11229T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066120 | ||||||
| chr4:118066120
|
TTATATAT others(25): Show |
T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.981+11237_981+1126 others(36): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066120 | |||||
| chr4:118066130
|
TATATA | T | 8 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+11245_981+1124 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066130 | |||||
| chr4:118066131
|
ATATAATA others(28): Show |
A | 5 | a0001c0004t0003g0205a0001c0004t0019g0195a0001c0016t0003g0215others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+11245_981+1127 others(39): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066131 | |||||
| chr4:118066136
|
A | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.981+11245A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066136 | ||||||
| chr4:118066142
|
TTTATATA others(39): Show |
T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+11265_981+1131 others(50): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066142 | |||||
| chr4:118066150
|
TTA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(10): Show | 13 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+11267_981+1126 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066150 | |||||
| chr4:118066156
|
ATATTATA others(25): Show |
A | 105 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0024others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.981+11267_981+1129 others(36): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066156 | |||||
| chr4:118066158
|
A | C | 2 | a0001c0001t0001g0141a0001c0001t0018g0162 | 2 | HG03130.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.981+11267A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066158 | ||||||
| chr4:118066166
|
T | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0121others(7): Show | 11 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11275T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066166 | ||||||
| chr4:118066172
|
T | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.981+11281T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066172 | ||||||
| chr4:118066173
|
T | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(10): Show | 13 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+11282T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066173 | ||||||
| chr4:118066182
|
ATATATCT | A | 9 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11297_981+1130 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066182 | |||||
| chr4:118066185
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11294T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066185 | ||||||
| chr4:118066186
|
ATC | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0058others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+11297_981+1129 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066186 | |||||
| chr4:118066188
|
C | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(36): Show | 40 | HG00544.hp2 HG00597.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.981+11297C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066188 | ||||||
| chr4:118066189
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11298T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066189 | ||||||
| chr4:118066192
|
T | C | 9 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11301T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066192 | ||||||
| chr4:118066195
|
A | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11304A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066195 | ||||||
| chr4:118066196
|
T | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(21): Show | 24 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.981+11305T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066196 | ||||||
| chr4:118066202
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11311T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066202 | ||||||
| chr4:118066203
|
T | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.981+11312T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066203 | ||||||
| chr4:118066206
|
T | C | 2 | a0001c0004t0003g0194a0001c0004t0003g0196 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.981+11315T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066206 | ||||||
| chr4:118066211
|
TATACATA | T | 10 | a0001c0001t0001g0121a0001c0004t0001g0197a0001c0004t0001g0199others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+11324_981+1133 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066211 | |||||
| chr4:118066213
|
TACATA | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11324_981+1132 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066213 | |||||
| chr4:118066215
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11324C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066215 | ||||||
| chr4:118066218
|
A | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11327A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066218 | ||||||
| chr4:118066219
|
A | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11328A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066219 | ||||||
| chr4:118066220
|
T | C | 10 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0005t0001g0107others(7): Show | 10 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+11329T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066220 | ||||||
| chr4:118066225
|
T | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11334T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066225 | ||||||
| chr4:118066226
|
A | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11335A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066226 | ||||||
| chr4:118066232
|
A | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(17): Show | 20 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.981+11341A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066232 | ||||||
| chr4:118066233
|
T | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 15 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11342T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066233 | ||||||
| chr4:118066233
|
TTATATAT others(18): Show |
T | 2 | a0001c0001t0001g0141a0001c0001t0001g0157 | 2 | HG00544.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.981+11387_981+1141 others(29): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066233 | |||||
| chr4:118066236
|
T | C | 5 | a0001c0004t0003g0205a0001c0004t0019g0195a0001c0016t0003g0215others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+11345T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066236 | ||||||
| chr4:118066243
|
T | TACATA | 5 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01433.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11353_981+1135 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066243 | |||||
| chr4:118066249
|
T | TTA | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+11364_981+1136 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066249 | |||||
| chr4:118066252
|
T | C | 1 | a0001c0004t0003g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.981+11361T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066252 | ||||||
| chr4:118066254
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.981+11363T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066254 | ||||||
| chr4:118066257
|
T | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(26): Show | 29 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.981+11366T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066257 | ||||||
| chr4:118066258
|
A | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(26): Show | 29 | HG00544.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.981+11367A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066258 | ||||||
| chr4:118066259
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.981+11368T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066259 | ||||||
| chr4:118066265
|
TTA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(10): Show | 13 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+11382_981+1138 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066265 | |||||
| chr4:118066266
|
T | A | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0005t0001g0109 | 3 | HG01070.hp1 HG01071.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.981+11375T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066266 | ||||||
| chr4:118066267
|
A | T | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0005t0001g0109 | 3 | HG01070.hp1 HG01071.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.981+11376A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066267 | ||||||
| chr4:118066267
|
ATATATAT | A | 3 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0108 | 3 | HG02615.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.981+11391_981+1139 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066267 | |||||
| chr4:118066273
|
A | G | 1 | a0001c0003t0002g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.981+11382A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066273 | ||||||
| chr4:118066273
|
A | T | 1 | a0001c0004t0003g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.981+11382A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066273 | ||||||
| chr4:118066274
|
T | A | 1 | a0001c0004t0003g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.981+11383T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066274 | ||||||
| chr4:118066278
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(45): Show | 49 | HG00558.hp1 HG00597.hp2 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.981+11387A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066278 | ||||||
| chr4:118066280
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(10): Show | 13 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+11389A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066280 | ||||||
| chr4:118066281
|
TTA | T | 3 | a0001c0004t0001g0197a0001c0004t0002g0198a0001c0016t0003g0215 | 3 | HG01109.hp2 HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+11398_981+1139 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066281 | |||||
| chr4:118066282
|
T | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.981+11391T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066282 | ||||||
| chr4:118066283
|
A | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 87 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.981+11392A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066283 | ||||||
| chr4:118066285
|
A | ATGT | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.981+11395_981+1139 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066285 | |||||
| chr4:118066287
|
A | G | 1 | a0001c0003t0002g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.981+11396A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066287 | ||||||
| chr4:118066288
|
TATTA | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(11): Show | 14 | HG00544.hp2 HG01071.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.981+11398_981+1140 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066288 | ||||||
| chr4:118066289
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+11398A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066289 | ||||||
| chr4:118066290
|
TTA | T | 10 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0196others(7): Show | 10 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+11407_981+1140 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066290 | |||||
| chr4:118066290
|
TTATATAT others(36): Show |
T | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11407_981+1144 others(47): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066290 | |||||
| chr4:118066291
|
T | A | 30 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(27): Show | 30 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.981+11400T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066291 | ||||||
| chr4:118066292
|
A | ATATAT | 33 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0024others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.981+11402_981+1140 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066292 | |||||
| chr4:118066292
|
A | T | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.981+11401A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066292 | ||||||
| chr4:118066294
|
ATATATTA others(27): Show |
A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+11407_981+1144 others(38): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066294 | |||||
| chr4:118066296
|
ATATTATG others(57): Show |
A | 1 | a0001c0002t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.981+11407_981+1147 others(68): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066296 | |||||
| chr4:118066297
|
TATTATGT others(4): Show |
T | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG00099.hp2 HG00558.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+11407_981+1141 others(15): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066297 | ||||||
| chr4:118066297
|
TATTATGT others(29): Show |
T | 20 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0079others(17): Show | 20 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.981+11407_981+1144 others(40): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066297 | ||||||
| chr4:118066298
|
A | G | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(45): Show | 48 | HG00544.hp2 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.981+11407A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066298 | ||||||
| chr4:118066298
|
A | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(10): Show | 13 | HG00639.hp2 HG01070.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+11407A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066298 | ||||||
| chr4:118066299
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(12): Show | 15 | HG00639.hp2 HG01070.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+11408T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066299 | ||||||
| chr4:118066299
|
TTATGTAT others(2): Show |
T | 3 | a0001c0003t0002g0020a0001c0004t0001g0197a0001c0004t0002g0198 | 3 | HG01884.hp1 HG02148.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+11412_981+1142 others(13): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066299 | |||||
| chr4:118066299
|
TTATGTAT others(27): Show |
T | 5 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0172others(2): Show | 5 | HG00639.hp1 HG02055.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11412_981+1144 others(38): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066299 | |||||
| chr4:118066303
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(87): Show | 90 | HG00544.hp2 HG00735.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.981+11412G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066303 | ||||||
| chr4:118066305
|
A | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG00639.hp2 HG01070.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11414A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066305 | ||||||
| chr4:118066306
|
T | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG00639.hp2 HG01070.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11415T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066306 | ||||||
| chr4:118066306
|
TTA | T | 2 | a0001c0004t0003g0194a0001c0005t0004g0108 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.981+11423_981+1142 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066306 | |||||
| chr4:118066307
|
T | A | 10 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0196others(7): Show | 10 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+11416T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066307 | ||||||
| chr4:118066308
|
A | T | 10 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0196others(7): Show | 10 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+11417A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066308 | ||||||
| chr4:118066310
|
A | AT | 11 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG00639.hp2 HG01070.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11420dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066310 | |||||
| chr4:118066310
|
A | ATGT | 33 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0024others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.981+11420_981+1142 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066310 | |||||
| chr4:118066313
|
TATTA | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(36): Show | 39 | HG00544.hp2 HG00738.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+11423_981+1142 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066313 | ||||||
| chr4:118066314
|
A | G | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 13 | HG00099.hp2 HG00558.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.981+11423A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066314 | ||||||
| chr4:118066316
|
T | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(41): Show | 44 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.981+11425T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066316 | ||||||
| chr4:118066316
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+11425T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066316 | ||||||
| chr4:118066317
|
A | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(41): Show | 44 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.981+11426A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066317 | ||||||
| chr4:118066322
|
TATTATGT others(4): Show |
T | 2 | a0001c0005t0001g0107a0001c0005t0004g0100 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.981+11432_981+1144 others(15): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066322 | ||||||
| chr4:118066323
|
A | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(43): Show | 47 | HG00558.hp1 HG00597.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.981+11432A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066323 | ||||||
| chr4:118066323
|
A | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(13): Show | 16 | HG00099.hp2 HG00558.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.981+11432A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066323 | ||||||
| chr4:118066324
|
T | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0030others(60): Show | 64 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.981+11433T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066324 | ||||||
| chr4:118066324
|
TTATGTAT others(2): Show |
T | 20 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(17): Show | 20 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.981+11437_981+1144 others(13): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066324 | |||||
| chr4:118066325
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+11434T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066325 | ||||||
| chr4:118066326
|
ATG | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0038others(25): Show | 28 | HG00544.hp2 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.981+11437_981+1143 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066326 | |||||
| chr4:118066327
|
T | TATC | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(42): Show | 46 | HG00558.hp1 HG00597.hp2 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.981+11436_981+1143 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066327 | ||||||
| chr4:118066327
|
T | TATCATAT others(24): Show |
1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.981+11436_981+1143 others(35): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066327 | ||||||
| chr4:118066328
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 102 | HG00558.hp1 HG00597.hp2 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.981+11437G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066328 | ||||||
| chr4:118066329
|
TATTA | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG00099.hp2 HG00558.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+11439_981+1144 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066329 | ||||||
| chr4:118066330
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+11439A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066330 | ||||||
| chr4:118066331
|
TTA | T | 4 | a0001c0002t0001g0078a0001c0002t0001g0170a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG02922.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+11448_981+1144 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066331 | |||||
| chr4:118066332
|
T | A | 2 | a0001c0001t0001g0121a0001c0004t0001g0206 | 2 | HG01975.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.981+11441T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066332 | ||||||
| chr4:118066332
|
T | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 75 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.981+11441T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066332 | ||||||
| chr4:118066333
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.981+11541_981+1156 others(32): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066333 | |||||
| chr4:118066333
|
A | ATATGT | 33 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0024others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.981+11445_981+1144 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066333 | |||||
| chr4:118066333
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 75 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.981+11442A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066333 | ||||||
| chr4:118066333
|
ATATATAT others(21): Show |
A | 4 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0165others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+11541_981+1156 others(32): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066333 | |||||
| chr4:118066336
|
T | C | 2 | a0001c0004t0003g0194a0001c0005t0001g0109 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.981+11445T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066336 | ||||||
| chr4:118066340
|
T | TTATATAT others(20): Show |
1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.981+11451_981+1147 others(31): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066340 | |||||
| chr4:118066346
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.981+11455A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066346 | ||||||
| chr4:118066348
|
C | A | 12 | a0001c0001t0001g0122a0001c0004t0001g0199a0001c0004t0001g0202others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11457C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066348 | ||||||
| chr4:118066348
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.981+11457C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066348 | ||||||
| chr4:118066349
|
A | T | 12 | a0001c0001t0001g0122a0001c0004t0001g0199a0001c0004t0001g0202others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11458A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066349 | ||||||
| chr4:118066349
|
ATATATCA others(5): Show |
A | 2 | a0001c0004t0003g0205a0001c0016t0003g0215 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.981+11464_981+1147 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066349 | |||||
| chr4:118066352
|
TATC | T | 12 | a0001c0001t0001g0122a0001c0004t0001g0199a0001c0004t0001g0202others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11464_981+1146 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066352 | |||||
| chr4:118066353
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.981+11462A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066353 | ||||||
| chr4:118066355
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.981+11464C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066355 | ||||||
| chr4:118066355
|
CAT | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+11467_981+1146 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066355 | |||||
| chr4:118066356
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.981+11465A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066356 | ||||||
| chr4:118066360
|
G | A | 2 | a0001c0001t0001g0121a0001c0004t0001g0206 | 2 | HG01975.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.981+11469G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066360 | ||||||
| chr4:118066360
|
G | T | 12 | a0001c0001t0001g0122a0001c0004t0001g0199a0001c0004t0001g0202others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11469G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066360 | ||||||
| chr4:118066361
|
T | A | 12 | a0001c0001t0001g0122a0001c0004t0001g0199a0001c0004t0001g0202others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11470T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066361 | ||||||
| chr4:118066364
|
T | C | 12 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+11473T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066364 | ||||||
| chr4:118066367
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.981+11476A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066367 | ||||||
| chr4:118066374
|
A | G | 63 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.981+11483A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066374 | ||||||
| chr4:118066376
|
C | A | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+11485C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066376 | ||||||
| chr4:118066376
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+11485C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066376 | ||||||
| chr4:118066377
|
A | T | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+11486A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066377 | ||||||
| chr4:118066381
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.981+11490A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066381 | ||||||
| chr4:118066383
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.981+11492C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066383 | ||||||
| chr4:118066388
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.981+11497G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066388 | ||||||
| chr4:118066388
|
G | T | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+11497G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066388 | ||||||
| chr4:118066389
|
T | A | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+11498T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066389 | ||||||
| chr4:118066392
|
T | C | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981+11501T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066392 | ||||||
| chr4:118066395
|
A | G | 23 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(20): Show | 23 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.981+11504A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066395 | ||||||
| chr4:118066397
|
TATATATC | T | 29 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0069others(26): Show | 29 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.981+11518_981+1152 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066397 | |||||
| chr4:118066402
|
A | G | 9 | a0001c0001t0014g0110a0001c0001t0017g0036a0001c0002t0001g0084others(6): Show | 9 | HG02602.hp2 HG02615.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+11511A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066402 | ||||||
| chr4:118066404
|
C | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 60 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.981+11513C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066404 | ||||||
| chr4:118066404
|
C | T | 44 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.981+11513C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066404 | ||||||
| chr4:118066409
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.981+11518A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066409 | ||||||
| chr4:118066410
|
TCA | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA18956.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.981+11520_981+1152 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066410 | ||||||
| chr4:118066411
|
C | A | 21 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(18): Show | 21 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.981+11520C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066411 | ||||||
| chr4:118066411
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.981+11520C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066411 | ||||||
| chr4:118066416
|
G | A | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.981+11525G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066416 | ||||||
| chr4:118066423
|
A | G | 27 | a0001c0001t0001g0176a0001c0001t0020g0113a0001c0002t0001g0002others(24): Show | 27 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.981+11532A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066423 | ||||||
| chr4:118066430
|
A | G | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+11539A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066430 | ||||||
| chr4:118066431
|
T | TA | 11 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0117others(8): Show | 12 | HG00558.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+11540_981+1154 others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066431 | ||||||
| chr4:118066432
|
C | A | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.981+11541C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066432 | ||||||
| chr4:118066432
|
C | T | 32 | a0001c0001t0001g0176a0001c0001t0014g0110a0001c0001t0020g0113others(29): Show | 32 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.981+11541C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066432 | ||||||
| chr4:118066434
|
TA | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0117others(8): Show | 12 | HG00558.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+11544delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066434 | ||||||
| chr4:118066437
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.981+11546A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066437 | ||||||
| chr4:118066438
|
TC | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0117others(8): Show | 12 | HG00558.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+11548delC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066438 | ||||||
| chr4:118066439
|
C | A | 24 | a0001c0001t0001g0176a0001c0001t0020g0113a0001c0002t0001g0002others(21): Show | 24 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.981+11548C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066439 | ||||||
| chr4:118066439
|
C | CATATGTT others(20): Show |
2 | a0001c0001t0001g0086a0001c0006t0001g0066 | 2 | HG02074.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.981+11634_981+1166 others(31): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066439 | |||||
| chr4:118066439
|
C | CATATGTT others(48): Show |
1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.981+11568_981+1156 others(59): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066439 | |||||
| chr4:118066439
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.981+11548C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066439 | ||||||
| chr4:118066439
|
CATATGTT others(20): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.981+11634_981+1166 others(31): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066439 | |||||
| chr4:118066451
|
A | G | 27 | a0001c0001t0001g0176a0001c0001t0020g0113a0001c0002t0001g0002others(24): Show | 27 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.981+11560A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066451 | ||||||
| chr4:118066457
|
TATACATT others(142): Show |
T | 2 | a0001c0005t0004g0100a0001c0005t0004g0108 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.981+11569_981+1171 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066457 | |||||
| chr4:118066458
|
A | AT | 5 | a0001c0001t0020g0113a0001c0004t0001g0206a0001c0005t0001g0107others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11568dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066458 | |||||
| chr4:118066458
|
A | G | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.981+11567A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066458 | ||||||
| chr4:118066459
|
T | TA | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0014g0110others(1): Show | 4 | HG03017.hp2 NA18947.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+11569dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066459 | |||||
| chr4:118066460
|
ACATTAT | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.981+11570_981+1157 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066460 | ||||||
| chr4:118066460
|
ACATTATA others(53): Show |
A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.981+11570_981+1162 others(64): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066460 | ||||||
| chr4:118066461
|
C | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0176others(7): Show | 10 | HG02258.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.981+11570C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066461 | ||||||
| chr4:118066464
|
T | A | 5 | a0001c0001t0020g0113a0001c0004t0001g0206a0001c0005t0001g0107others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11573T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066464 | ||||||
| chr4:118066464
|
T | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0014g0110others(1): Show | 4 | HG03017.hp2 NA18947.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+11573T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066464 | ||||||
| chr4:118066465
|
A | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0014g0110others(6): Show | 9 | HG02258.hp2 HG02630.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+11574A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066465 | ||||||
| chr4:118066465
|
ATATATGT others(18): Show |
A | 1 | a0001c0002t0001g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.981+11580_981+1160 others(29): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066465 | |||||
| chr4:118066466
|
T | A | 2 | a0001c0001t0020g0113a0001c0004t0001g0206 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.981+11575T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066466 | ||||||
| chr4:118066470
|
TGTTATAT others(205): Show |
T | 19 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(16): Show | 19 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+11580_981+1179 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066470 | ||||||
| chr4:118066478
|
A | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.981+11587A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066478 | ||||||
| chr4:118066486
|
T | TA | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11596dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066486 | |||||
| chr4:118066487
|
ACATTAT | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18972.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.981+11597_981+1160 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066487 | ||||||
| chr4:118066488
|
C | T | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11597C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066488 | ||||||
| chr4:118066490
|
T | TTA | 94 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.981+11605_981+1160 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066490 | |||||
| chr4:118066491
|
T | G | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11600T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066491 | ||||||
| chr4:118066492
|
A | T | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11601A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066492 | ||||||
| chr4:118066493
|
T | TATATAAT others(62): Show |
1 | a0001c0001t0001g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.981+11606_981+1160 others(73): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066493 | |||||
| chr4:118066493
|
TATATGTT others(52): Show |
T | 2 | a0001c0004t0019g0195a0001c0007t0001g0203 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.981+11634_981+1169 others(63): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066493 | |||||
| chr4:118066495
|
TATGTTAT others(84): Show |
T | 9 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11634_981+1172 others(95): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066495 | |||||
| chr4:118066495
|
TATGTTAT others(212): Show |
T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.981+11634_981+1185 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066495 | |||||
| chr4:118066497
|
TGTTATAT others(15): Show |
T | 2 | a0001c0004t0003g0194a0001c0017t0001g0207 | 2 | HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.981+11607_981+1162 others(26): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066497 | ||||||
| chr4:118066505
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.981+11614A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066505 | ||||||
| chr4:118066511
|
TATACATT others(120): Show |
T | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.981+11623_981+1174 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066511 | |||||
| chr4:118066514
|
ACATTAT | A | 2 | a0001c0001t0014g0110a0001c0003t0002g0007 | 2 | HG03017.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.981+11624_981+1162 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066514 | ||||||
| chr4:118066520
|
T | A | 2 | a0001c0004t0003g0194a0001c0017t0001g0207 | 2 | HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.981+11629T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066520 | ||||||
| chr4:118066520
|
T | TATATA | 7 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0140others(4): Show | 7 | HG01884.hp1 HG02004.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+11633_981+1163 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066520 | |||||
| chr4:118066520
|
T | TATATAAT others(30): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.981+11633_981+1163 others(41): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066520 | |||||
| chr4:118066520
|
T | TATATAAT others(94): Show |
1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.981+11633_981+1163 others(105): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066520 | |||||
| chr4:118066520
|
T | TATATGTT others(25): Show |
8 | a0001c0001t0001g0114a0001c0001t0001g0128a0001c0001t0001g0131others(5): Show | 8 | HG01891.hp2 NA18612.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+11663_981+1169 others(36): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066520 | |||||
| chr4:118066522
|
T | TATAATAT others(30): Show |
1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.981+11633_981+1163 others(41): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066522 | |||||
| chr4:118066522
|
T | TATAATAT others(126): Show |
1 | a0001c0001t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.981+11633_981+1163 others(137): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066522 | |||||
| chr4:118066522
|
T | TATGTTAT others(57): Show |
1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981+11662_981+1166 others(68): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066522 | |||||
| chr4:118066524
|
TGTTATAT others(214): Show |
T | 1 | a0001c0002t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.981+11634_981+1185 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066524 | ||||||
| chr4:118066532
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.981+11641A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066532 | ||||||
| chr4:118066538
|
TATAC | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(5): Show | 8 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+11650_981+1165 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066538 | |||||
| chr4:118066547
|
TATATA | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0165others(1): Show | 4 | HG01433.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+11661_981+1166 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066547 | |||||
| chr4:118066549
|
TATAATAT others(62): Show |
T | 1 | a0001c0008t0003g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.981+11661_981+1172 others(73): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066549 | |||||
| chr4:118066554
|
T | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0175a0001c0001t0001g0187others(2): Show | 5 | HG00558.hp1 HG01175.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+11663T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066554 | ||||||
| chr4:118066554
|
T | TATGTTAT others(89): Show |
1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.981+11971_981+1206 others(100): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
T | TATGTTAT others(57): Show |
1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.981+11694_981+1169 others(68): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
T | TATGTTAT others(89): Show |
1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.981+11694_981+1169 others(100): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
T | TATGTTAT others(89): Show |
1 | a0001c0001t0008g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.981+11694_981+1169 others(100): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
TATGTTAT others(25): Show |
T | 3 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0012g0115 | 3 | HG02647.hp2 NA19068.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.981+12035_981+1206 others(36): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
TATGTTAT others(89): Show |
T | 2 | a0001c0004t0002g0198a0001c0005t0001g0109 | 2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.981+11971_981+1206 others(100): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066554
|
TATGTTAT others(156): Show |
T | 1 | a0001c0005t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.981+11664_981+1182 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066554 | ||||||
| chr4:118066554
|
TATGTTAT others(185): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.981+11875_981+1206 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066554 | |||||
| chr4:118066564
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11673A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066564 | ||||||
| chr4:118066583
|
TAAC | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.981+11694_981+1169 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066583 | |||||
| chr4:118066584
|
AAC | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0024others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.981+11695_981+1169 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066584 | |||||
| chr4:118066584
|
AACATGTT others(155): Show |
A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+11695_981+1185 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066584 | |||||
| chr4:118066585
|
ACAT | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG01169.hp2 HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.981+11695_981+1169 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066585 | ||||||
| chr4:118066586
|
C | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.981+11695C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066586 | ||||||
| chr4:118066589
|
G | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG01169.hp2 HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.981+11698G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066589 | ||||||
| chr4:118066590
|
TTA | T | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.981+11705_981+1170 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066590 | |||||
| chr4:118066591
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.981+11700T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066591 | ||||||
| chr4:118066593
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.981+11702T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066593 | ||||||
| chr4:118066596
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(5): Show | 8 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+11705A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066596 | ||||||
| chr4:118066598
|
T | A | 2 | a0001c0001t0001g0117a0001c0003t0002g0018 | 2 | HG01433.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.981+11707T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066598 | ||||||
| chr4:118066613
|
TATAAC | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0057others(2): Show | 5 | HG02602.hp1 NA18947.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11725_981+1172 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066613 | |||||
| chr4:118066615
|
TAAC | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0017g0036 | 3 | HG00558.hp2 HG01192.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.981+11726_981+1172 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066615 | |||||
| chr4:118066616
|
AAC | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.981+11727_981+1172 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066616 | |||||
| chr4:118066618
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0116others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.981+11727C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066618 | ||||||
| chr4:118066621
|
GT | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.981+11732delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066621 | |||||
| chr4:118066622
|
TTA | T | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.981+11737_981+1173 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066622 | |||||
| chr4:118066627
|
TATTATAT others(100): Show |
T | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.981+11747_981+1185 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066627 | |||||
| chr4:118066628
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0057a0001c0001t0014g0110others(3): Show | 6 | HG01192.hp2 HG02615.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.981+11737A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066628 | ||||||
| chr4:118066630
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.981+11739T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066630 | ||||||
| chr4:118066645
|
TATAAC | T | 2 | a0001c0001t0001g0033a0001c0001t0017g0036 | 2 | HG01192.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.981+11757_981+1176 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066645 | |||||
| chr4:118066645
|
TATAACAT others(190): Show |
T | 1 | a0001c0002t0001g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.981+11757_981+1195 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066645 | |||||
| chr4:118066647
|
TAA | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG00558.hp2 HG02602.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+11757_981+1175 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066647 | ||||||
| chr4:118066647
|
TAAC | T | 2 | a0001c0005t0004g0100a0001c0005t0004g0108 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.981+11758_981+1176 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066647 | |||||
| chr4:118066647
|
TAACATGT others(220): Show |
T | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.981+11758_981+1198 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066647 | |||||
| chr4:118066648
|
AAC | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 68 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.981+11759_981+1176 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066648 | |||||
| chr4:118066650
|
C | T | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.981+11759C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066650 | ||||||
| chr4:118066653
|
GT | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 67 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.981+11764delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066653 | |||||
| chr4:118066660
|
A | G | 5 | a0001c0001t0001g0057a0001c0001t0017g0036a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+11769A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066660 | ||||||
| chr4:118066677
|
TATAAC | T | 3 | a0001c0001t0017g0036a0001c0005t0004g0100a0001c0005t0004g0108 | 3 | HG02615.hp1 HG03195.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.981+11789_981+1179 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066677 | |||||
| chr4:118066677
|
TATAACAT others(94): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.981+11789_981+1188 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066677 | |||||
| chr4:118066679
|
TAACATGT others(188): Show |
T | 22 | a0001c0001t0001g0121a0001c0002t0001g0061a0001c0002t0001g0081others(19): Show | 22 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+11790_981+1198 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066679 | |||||
| chr4:118066680
|
AAC | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(8): Show | 11 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11791_981+1179 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066680 | |||||
| chr4:118066682
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(81): Show | 84 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.981+11791C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066682 | ||||||
| chr4:118066685
|
GT | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0054others(3): Show | 6 | HG03017.hp2 NA18960.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.981+11796delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066685 | |||||
| chr4:118066691
|
T | C | 1 | a0001c0003t0002g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.981+11800T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066691 | ||||||
| chr4:118066692
|
A | G | 21 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(18): Show | 21 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.981+11801A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066692 | ||||||
| chr4:118066699
|
A | G | 9 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0196others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11808A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066699 | ||||||
| chr4:118066705
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.981+11814T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066705 | ||||||
| chr4:118066709
|
TATAAC | T | 21 | a0001c0001t0001g0055a0001c0001t0001g0176a0001c0002t0001g0002others(18): Show | 21 | HG00738.hp2 HG01070.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.981+11821_981+1182 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066709 | |||||
| chr4:118066709
|
TATAACAT others(30): Show |
T | 1 | a0001c0011t0009g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.981+11821_981+1185 others(41): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066709 | |||||
| chr4:118066709
|
TATAACAT others(62): Show |
T | 5 | a0001c0001t0015g0049a0001c0003t0002g0019a0001c0003t0002g0020others(2): Show | 5 | HG02004.hp2 HG02148.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+11821_981+1188 others(73): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066709 | |||||
| chr4:118066709
|
TATAACAT others(94): Show |
T | 49 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(46): Show | 49 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.981+11821_981+1192 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066709 | |||||
| chr4:118066711
|
TAACATGT others(156): Show |
T | 6 | a0001c0001t0001g0184a0001c0002t0001g0069a0001c0002t0001g0070others(3): Show | 6 | HG00639.hp1 HG02055.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+11822_981+1198 others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066711 | |||||
| chr4:118066712
|
AAC | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.981+11823_981+1182 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066712 | |||||
| chr4:118066714
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0045others(24): Show | 27 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.981+11823C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066714 | ||||||
| chr4:118066717
|
GT | G | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG01192.hp2 HG02602.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+11828delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066717 | |||||
| chr4:118066724
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.981+11833A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066724 | ||||||
| chr4:118066727
|
ATATATAC others(87): Show |
A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.981+11843_981+1193 others(98): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066727 | |||||
| chr4:118066728
|
T | C | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.981+11837T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066728 | ||||||
| chr4:118066731
|
A | G | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.981+11840A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066731 | ||||||
| chr4:118066741
|
TATAACAT others(30): Show |
T | 1 | a0001c0001t0001g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.981+11853_981+1188 others(41): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066741 | |||||
| chr4:118066741
|
TATAACAT others(62): Show |
T | 6 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(3): Show | 6 | HG01192.hp1 NA18960.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.981+11853_981+1192 others(73): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066741 | |||||
| chr4:118066744
|
AAC | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 12 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+11855_981+1185 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066744 | |||||
| chr4:118066746
|
C | A | 1 | a0001c0002t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.981+11855C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066746 | ||||||
| chr4:118066746
|
C | T | 39 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(36): Show | 39 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.981+11855C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066746 | ||||||
| chr4:118066749
|
GT | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG00558.hp2 HG01192.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+11860delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066749 | |||||
| chr4:118066766
|
C | A | 1 | a0001c0005t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.981+11875C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066766 | ||||||
| chr4:118066776
|
AAC | A | 24 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(21): Show | 24 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.981+11887_981+1188 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066776 | |||||
| chr4:118066778
|
C | T | 30 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 30 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.981+11887C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066778 | ||||||
| chr4:118066781
|
G | T | 1 | a0001c0002t0001g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.981+11890G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066781 | ||||||
| chr4:118066781
|
GT | G | 5 | a0001c0002t0001g0078a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+11892delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066781 | |||||
| chr4:118066790
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.981+11899T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066790 | ||||||
| chr4:118066796
|
T | C | 1 | a0001c0001t0001g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.981+11905T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066796 | ||||||
| chr4:118066805
|
TATAAC | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00099.hp2 HG00558.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+11917_981+1192 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066805 | |||||
| chr4:118066808
|
AAC | A | 25 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(22): Show | 25 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+11919_981+1192 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066808 | |||||
| chr4:118066810
|
C | T | 29 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0125others(26): Show | 29 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.981+11919C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066810 | ||||||
| chr4:118066813
|
GT | G | 25 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(22): Show | 25 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+11924delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066813 | |||||
| chr4:118066837
|
TATAAC | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0185others(1): Show | 4 | HG00099.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+11949_981+1195 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066837 | |||||
| chr4:118066842
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.981+11951C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066842 | ||||||
| chr4:118066846
|
T | G | 1 | a0001c0009t0003g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.981+11955T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066846 | ||||||
| chr4:118066860
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0147 | 3 | HG01256.hp1 HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.981+11969T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066860 | ||||||
| chr4:118066871
|
TAAC | T | 26 | a0001c0001t0001g0176a0001c0002t0001g0002a0001c0002t0001g0029others(23): Show | 26 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.981+11982_981+1198 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118066871 | |||||
| chr4:118066874
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 93 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.981+11983C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066874 | ||||||
| chr4:118066886
|
TATATATA others(55): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.981+11996_981+1205 others(66): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066886 | ||||||
| chr4:118066906
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.981+12015C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066906 | ||||||
| chr4:118066938
|
C | A | 1 | a0001c0002t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.981+12047C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066938 | ||||||
| chr4:118066938
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.981+12047C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066938 | ||||||
| chr4:118066951
|
A | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.981+12060A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118066951 | ||||||
| chr4:118067034
|
C | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+12143C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067034 | ||||||
| chr4:118067155
|
T | C | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.981+12264T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067155 | ||||||
| chr4:118067273
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.981+12382T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067273 | ||||||
| chr4:118067462
|
T | A | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981+12571T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067462 | ||||||
| chr4:118067525
|
T | C | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.981+12634T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067525 | ||||||
| chr4:118067544
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.981+12653A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067544 | ||||||
| chr4:118067635
|
A | C | 1 | a0001c0003t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.981+12744A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067635 | ||||||
| chr4:118067854
|
C | A | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.981+12963C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067854 | ||||||
| chr4:118067867
|
C | A | 4 | a0001c0007t0001g0200a0001c0007t0001g0201a0001c0007t0001g0203others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+12976C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067867 | ||||||
| chr4:118067959
|
G | C | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+13068G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118067959 | ||||||
| chr4:118068166
|
C | CT | 62 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(59): Show | 62 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.981+13299dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118068166 | |||||
| chr4:118068166
|
C | CTT | 9 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0044others(6): Show | 9 | HG00099.hp2 HG01169.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+13298_981+1329 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118068166 | |||||
| chr4:118068166
|
CT | C | 56 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0001g0127others(53): Show | 56 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.981+13299delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118068166 | |||||
| chr4:118068312
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+13421G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118068312 | ||||||
| chr4:118068488
|
A | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+13597A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118068488 | ||||||
| chr4:118068988
|
C | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+14097C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118068988 | ||||||
| chr4:118069117
|
G | A | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.981+14226G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069117 | ||||||
| chr4:118069143
|
GATCA | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.981+14253_981+1425 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069143 | ||||||
| chr4:118069204
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.981+14313T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069204 | ||||||
| chr4:118069276
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.981+14385A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069276 | ||||||
| chr4:118069355
|
C | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+14464C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069355 | ||||||
| chr4:118069791
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+14900C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069791 | ||||||
| chr4:118069813
|
C | CCAAT | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+14924_981+1492 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118069813 | |||||
| chr4:118069867
|
TTTG | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+14982_981+1498 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118069867 | |||||
| chr4:118069937
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+15046A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118069937 | ||||||
| chr4:118070036
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+15145C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118070036 | ||||||
| chr4:118070145
|
C | G | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.981+15254C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118070145 | ||||||
| chr4:118070647
|
C | CT | 11 | a0001c0002t0001g0068a0001c0002t0001g0173a0001c0005t0001g0107others(8): Show | 11 | HG00738.hp2 HG02615.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+15770dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118070647 | |||||
| chr4:118070647
|
CT | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0111a0001c0001t0015g0049others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+15770delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118070647 | |||||
| chr4:118070916
|
C | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0185others(1): Show | 4 | HG00099.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+16025C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118070916 | ||||||
| chr4:118070993
|
C | T | 1 | a0001c0003t0007g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.981+16102C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118070993 | ||||||
| chr4:118071040
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+16149G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071040 | ||||||
| chr4:118071118
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+16227C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071118 | ||||||
| chr4:118071212
|
G | A | 1 | a0001c0003t0002g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.981+16321G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071212 | ||||||
| chr4:118071243
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+16352T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071243 | ||||||
| chr4:118071270
|
T | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+16379T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071270 | ||||||
| chr4:118071294
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.981+16403G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071294 | ||||||
| chr4:118071490
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+16599C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071490 | ||||||
| chr4:118071687
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+16796T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071687 | ||||||
| chr4:118071788
|
G | A | 2 | a0001c0002t0001g0087a0001c0005t0004g0106 | 2 | HG03041.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.981+16897G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071788 | ||||||
| chr4:118071912
|
T | C | 1 | a0001c0001t0013g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.981+17021T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118071912 | ||||||
| chr4:118072328
|
A | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+17437A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118072328 | ||||||
| chr4:118073011
|
T | A | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.981+18120T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118073011 | ||||||
| chr4:118073067
|
G | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.981+18176G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118073067 | ||||||
| chr4:118073233
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+18342A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118073233 | ||||||
| chr4:118073565
|
A | G | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.981+18674A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118073565 | ||||||
| chr4:118074240
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+19349C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074240 | ||||||
| chr4:118074456
|
A | C | 1 | a0001c0002t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.981+19565A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074456 | ||||||
| chr4:118074666
|
T | C | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.981+19775T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074666 | ||||||
| chr4:118074745
|
G | T | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+19854G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074745 | ||||||
| chr4:118074781
|
G | T | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981+19890G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074781 | ||||||
| chr4:118074950
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+20059A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074950 | ||||||
| chr4:118074960
|
G | C | 12 | a0001c0001t0001g0024a0001c0003t0002g0012a0001c0003t0002g0013others(9): Show | 12 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+20069G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118074960 | ||||||
| chr4:118075071
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+20180G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118075071 | ||||||
| chr4:118075527
|
GTTC | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+20639_981+2064 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118075527 | |||||
| chr4:118075749
|
GATT | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+20859_981+2086 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118075749 | ||||||
| chr4:118076147
|
G | T | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.981+21256G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118076147 | ||||||
| chr4:118076439
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+21548C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118076439 | ||||||
| chr4:118076467
|
A | AT | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+21578dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118076467 | |||||
| chr4:118076667
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+21776C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118076667 | ||||||
| chr4:118076830
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+21939C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118076830 | ||||||
| chr4:118076899
|
C | T | 1 | a0001c0001t0018g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.981+22008C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118076899 | ||||||
| chr4:118077057
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.981+22166G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077057 | ||||||
| chr4:118077070
|
A | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.981+22179A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077070 | ||||||
| chr4:118077136
|
T | C | 1 | a0001c0003t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.981+22245T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077136 | ||||||
| chr4:118077435
|
C | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+22544C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077435 | ||||||
| chr4:118077479
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+22588G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077479 | ||||||
| chr4:118077509
|
G | T | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.981+22618G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077509 | ||||||
| chr4:118077519
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.981+22628G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077519 | ||||||
| chr4:118077601
|
A | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+22710A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077601 | ||||||
| chr4:118077623
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+22732A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077623 | ||||||
| chr4:118077639
|
C | T | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+22748C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077639 | ||||||
| chr4:118077643
|
G | A | 52 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(49): Show | 52 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.981+22752G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077643 | ||||||
| chr4:118077714
|
C | T | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.981+22823C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077714 | ||||||
| chr4:118077896
|
C | T | 1 | a0001c0002t0001g0096 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.981+23005C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077896 | ||||||
| chr4:118077897
|
T | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.981+23006T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118077897 | ||||||
| chr4:118078144
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.981+23253G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078144 | ||||||
| chr4:118078248
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+23357T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078248 | ||||||
| chr4:118078302
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+23411G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078302 | ||||||
| chr4:118078325
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+23434G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078325 | ||||||
| chr4:118078410
|
G | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.981+23519G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078410 | ||||||
| chr4:118078518
|
G | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+23627G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078518 | ||||||
| chr4:118078681
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+23790A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078681 | ||||||
| chr4:118078744
|
G | GA | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.981+23868dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118078744 | |||||
| chr4:118078878
|
A | T | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.981+23987A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118078878 | ||||||
| chr4:118079141
|
A | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.981+24250A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079141 | ||||||
| chr4:118079221
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.981+24330C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079221 | ||||||
| chr4:118079264
|
G | A | 1 | a0001c0003t0002g0169 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.981+24373G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079264 | ||||||
| chr4:118079279
|
G | A | 2 | a0001c0010t0003g0171a0001c0010t0003g0213 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.981+24388G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079279 | ||||||
| chr4:118079336
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.981+24445G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079336 | ||||||
| chr4:118079507
|
C | T | 16 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.981+24616C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079507 | ||||||
| chr4:118079645
|
C | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.981+24754C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079645 | ||||||
| chr4:118079678
|
G | T | 18 | a0001c0004t0001g0197a0001c0004t0001g0199a0001c0004t0001g0202others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.981+24787G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079678 | ||||||
| chr4:118079731
|
G | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+24840G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118079731 | ||||||
| chr4:118080105
|
T | G | 1 | a0001c0001t0001g0050 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.982-24913T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080105 | ||||||
| chr4:118080154
|
C | T | 1 | a0001c0001t0018g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.982-24864C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080154 | ||||||
| chr4:118080169
|
A | C | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.982-24849A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080169 | ||||||
| chr4:118080292
|
G | A | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.982-24726G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080292 | ||||||
| chr4:118080358
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.982-24660C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080358 | ||||||
| chr4:118080412
|
G | A | 56 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(53): Show | 56 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.982-24606G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080412 | ||||||
| chr4:118080470
|
A | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.982-24548A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080470 | ||||||
| chr4:118080472
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.982-24546A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080472 | ||||||
| chr4:118080509
|
T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0041others(4): Show | 7 | HG00544.hp2 HG02165.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-24509T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080509 | ||||||
| chr4:118080517
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-24501T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080517 | ||||||
| chr4:118080567
|
G | A | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.982-24451G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080567 | ||||||
| chr4:118080569
|
A | C | 1 | a0001c0002t0001g0095 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.982-24449A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080569 | ||||||
| chr4:118080767
|
T | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-24251T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118080767 | ||||||
| chr4:118081028
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0211 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.982-23990C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081028 | ||||||
| chr4:118081034
|
A | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-23984A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081034 | ||||||
| chr4:118081066
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-23952C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081066 | ||||||
| chr4:118081076
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-23942C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081076 | ||||||
| chr4:118081156
|
G | A | 1 | a0001c0005t0004g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982-23862G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081156 | ||||||
| chr4:118081259
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.982-23759T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081259 | ||||||
| chr4:118081369
|
A | G | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-23649A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081369 | ||||||
| chr4:118081410
|
TTG | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-23595_982-2359 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118081410 | |||||
| chr4:118081562
|
A | C | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-23456A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081562 | ||||||
| chr4:118081608
|
G | A | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.982-23410G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081608 | ||||||
| chr4:118081624
|
G | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-23394G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081624 | ||||||
| chr4:118081671
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0150a0001c0001t0001g0165others(1): Show | 4 | HG01433.hp1 HG01975.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-23347C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081671 | ||||||
| chr4:118081789
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-23229C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081789 | ||||||
| chr4:118081849
|
C | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-23169C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081849 | ||||||
| chr4:118081969
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.982-23049T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118081969 | ||||||
| chr4:118082225
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-22793A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082225 | ||||||
| chr4:118082378
|
T | A | 13 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0088others(10): Show | 13 | HG00597.hp1 NA18747.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.982-22640T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082378 | ||||||
| chr4:118082378
|
T | G | 20 | a0001c0002t0001g0029a0001c0002t0001g0060a0001c0002t0001g0064others(17): Show | 20 | HG00099.hp1 HG00735.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.982-22640T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082378 | ||||||
| chr4:118082525
|
T | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0068others(5): Show | 8 | HG00639.hp1 HG00738.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-22493T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082525 | ||||||
| chr4:118082645
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-22373T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082645 | ||||||
| chr4:118082688
|
C | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-22330C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082688 | ||||||
| chr4:118082746
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-22272T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082746 | ||||||
| chr4:118082860
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG00558.hp2 NA18984.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.982-22158A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118082860 | ||||||
| chr4:118083125
|
T | C | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-21893T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083125 | ||||||
| chr4:118083274
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | NA18945.hp2 NA18956.hp2 NA18999.hp2 others(5): Show |
intron_variant | MODIFIER | c.982-21744C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083274 | ||||||
| chr4:118083275
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-21743A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083275 | ||||||
| chr4:118083428
|
T | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.982-21590T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083428 | ||||||
| chr4:118083533
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-21485C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083533 | ||||||
| chr4:118083729
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-21289C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083729 | ||||||
| chr4:118083848
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.982-21170G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083848 | ||||||
| chr4:118083893
|
C | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-21125C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118083893 | ||||||
| chr4:118084034
|
G | T | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-20984G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084034 | ||||||
| chr4:118084121
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.982-20897C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084121 | ||||||
| chr4:118084145
|
C | T | 1 | a0001c0004t0003g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.982-20873C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084145 | ||||||
| chr4:118084245
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.982-20773A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084245 | ||||||
| chr4:118084259
|
T | A | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.982-20759T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084259 | ||||||
| chr4:118084307
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.982-20711T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084307 | ||||||
| chr4:118084428
|
A | C | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-20590A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084428 | ||||||
| chr4:118084568
|
G | A | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.982-20450G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084568 | ||||||
| chr4:118084858
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.982-20160C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084858 | ||||||
| chr4:118084947
|
C | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-20071C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084947 | ||||||
| chr4:118084980
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982-20038C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118084980 | ||||||
| chr4:118085018
|
G | A | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.982-20000G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118085018 | ||||||
| chr4:118085110
|
G | A | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-19908G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118085110 | ||||||
| chr4:118085122
|
A | AAAC | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-19877_982-1987 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118085122 | |||||
| chr4:118085625
|
C | CATTGTTG others(16): Show |
1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-19377_982-1935 others(27): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118085625 | |||||
| chr4:118085808
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.982-19210C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118085808 | ||||||
| chr4:118086151
|
A | T | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-18867A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086151 | ||||||
| chr4:118086331
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.982-18687A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086331 | ||||||
| chr4:118086382
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.982-18636G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086382 | ||||||
| chr4:118086483
|
C | G | 1 | a0001c0003t0002g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.982-18535C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086483 | ||||||
| chr4:118086665
|
C | T | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-18353C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086665 | ||||||
| chr4:118086744
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.982-18274T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086744 | ||||||
| chr4:118086746
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.982-18272A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086746 | ||||||
| chr4:118086876
|
A | G | 1 | a0001c0003t0002g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.982-18142A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086876 | ||||||
| chr4:118086903
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-18115C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118086903 | ||||||
| chr4:118087150
|
T | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.982-17868T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087150 | ||||||
| chr4:118087273
|
T | C | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-17745T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087273 | ||||||
| chr4:118087301
|
C | G | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-17717C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087301 | ||||||
| chr4:118087314
|
T | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-17704T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087314 | ||||||
| chr4:118087362
|
G | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-17656G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087362 | ||||||
| chr4:118087402
|
A | G | 13 | a0001c0004t0001g0199a0001c0004t0001g0202a0001c0004t0003g0194others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.982-17616A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087402 | ||||||
| chr4:118087926
|
T | C | 1 | a0001c0001t0016g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.982-17092T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087926 | ||||||
| chr4:118087983
|
T | A | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-17035T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118087983 | ||||||
| chr4:118088001
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.982-17017T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088001 | ||||||
| chr4:118088062
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-16956A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088062 | ||||||
| chr4:118088064
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-16954C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088064 | ||||||
| chr4:118088315
|
T | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-16703T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088315 | ||||||
| chr4:118088597
|
T | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-16421T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088597 | ||||||
| chr4:118088686
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-16332A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088686 | ||||||
| chr4:118088739
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-16279T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088739 | ||||||
| chr4:118088791
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-16227G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118088791 | ||||||
| chr4:118089055
|
A | G | 12 | a0001c0004t0001g0197a0001c0004t0002g0198a0001c0004t0003g0194others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.982-15963A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089055 | ||||||
| chr4:118089265
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0054 | 2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.982-15753A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089265 | ||||||
| chr4:118089656
|
A | T | 1 | a0001c0010t0003g0171 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.982-15362A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089656 | ||||||
| chr4:118089753
|
G | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-15265G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089753 | ||||||
| chr4:118089822
|
T | C | 1 | a0001c0003t0002g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.982-15196T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089822 | ||||||
| chr4:118089987
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-15031G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118089987 | ||||||
| chr4:118090287
|
G | A | 33 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.982-14731G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118090287 | ||||||
| chr4:118090288
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-14730T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118090288 | ||||||
| chr4:118090502
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.982-14516C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118090502 | ||||||
| chr4:118090738
|
A | C | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-14280A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118090738 | ||||||
| chr4:118090965
|
C | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.982-14053C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118090965 | ||||||
| chr4:118091118
|
T | C | 48 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.982-13900T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091118 | ||||||
| chr4:118091366
|
A | G | 1 | a0001c0010t0003g0171 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.982-13652A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091366 | ||||||
| chr4:118091693
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-13325T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091693 | ||||||
| chr4:118091762
|
G | C | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.982-13256G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091762 | ||||||
| chr4:118091847
|
TCTA | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-13167_982-1316 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118091847 | |||||
| chr4:118091855
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-13163G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091855 | ||||||
| chr4:118091999
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.982-13019A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118091999 | ||||||
| chr4:118092012
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18972.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.982-13006T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092012 | ||||||
| chr4:118092049
|
CTTAT | C | 12 | a0001c0004t0001g0197a0001c0004t0002g0198a0001c0004t0003g0194others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.982-12943_982-1294 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118092049 | |||||
| chr4:118092056
|
A | ATTTATTT others(9): Show |
2 | a0001c0001t0001g0033a0001c0003t0002g0022 | 2 | HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.982-12947_982-1294 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118092056 | |||||
| chr4:118092056
|
A | ATTTATTT others(5): Show |
129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.982-12951_982-1295 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118092056 | |||||
| chr4:118092075
|
T | C | 8 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.982-12943T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092075 | ||||||
| chr4:118092169
|
C | T | 1 | a0001c0005t0004g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982-12849C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092169 | ||||||
| chr4:118092212
|
A | G | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.982-12806A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092212 | ||||||
| chr4:118092225
|
G | GT | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.982-12782dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118092225 | |||||
| chr4:118092439
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-12579G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092439 | ||||||
| chr4:118092598
|
C | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-12420C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092598 | ||||||
| chr4:118092910
|
T | A | 33 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.982-12108T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118092910 | ||||||
| chr4:118093025
|
G | GA | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.982-11989dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118093025 | |||||
| chr4:118093030
|
T | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.982-11988T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093030 | ||||||
| chr4:118093083
|
A | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-11935A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093083 | ||||||
| chr4:118093326
|
T | C | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-11692T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093326 | ||||||
| chr4:118093352
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.982-11666A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093352 | ||||||
| chr4:118093421
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-11597T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093421 | ||||||
| chr4:118093470
|
A | G | 1 | a0001c0006t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982-11548A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093470 | ||||||
| chr4:118093711
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-11307T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118093711 | ||||||
| chr4:118094043
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-10975T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094043 | ||||||
| chr4:118094087
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.982-10931C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094087 | ||||||
| chr4:118094112
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.982-10906T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094112 | ||||||
| chr4:118094135
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.982-10883G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094135 | ||||||
| chr4:118094226
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-10792T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094226 | ||||||
| chr4:118094251
|
A | ATTAAAGT others(2): Show |
2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.982-10763_982-1075 others(13): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118094251 | |||||
| chr4:118094299
|
C | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.982-10719C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094299 | ||||||
| chr4:118094319
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.982-10699G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094319 | ||||||
| chr4:118094521
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.982-10497G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094521 | ||||||
| chr4:118094677
|
C | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.982-10341C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094677 | ||||||
| chr4:118094903
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.982-10115C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094903 | ||||||
| chr4:118094908
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-10110C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118094908 | ||||||
| chr4:118095062
|
T | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.982-9956T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118095062 | ||||||
| chr4:118095424
|
T | C | 1 | a0001c0002t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.982-9594T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118095424 | ||||||
| chr4:118095938
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.982-9080A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118095938 | ||||||
| chr4:118096139
|
G | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-8879G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096139 | ||||||
| chr4:118096207
|
C | G | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.982-8811C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096207 | ||||||
| chr4:118096268
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-8750G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096268 | ||||||
| chr4:118096505
|
A | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-8513A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096505 | ||||||
| chr4:118096659
|
G | GTAGA | 41 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.982-8310_982-8307d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096659 | |||||
| chr4:118096659
|
G | GTAGATAG others(1): Show |
9 | a0001c0001t0001g0059a0001c0001t0001g0125a0001c0001t0001g0127others(6): Show | 9 | HG02027.hp2 HG02165.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-8314_982-8307d others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096659 | |||||
| chr4:118096659
|
GTAGA | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(62): Show | 65 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.982-8310_982-8307d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096659 | |||||
| chr4:118096659
|
GTAGATAG others(1): Show |
G | 5 | a0001c0001t0001g0120a0001c0001t0017g0036a0001c0001t0018g0162others(2): Show | 5 | HG02896.hp1 HG03130.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.982-8314_982-8307d others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096659 | |||||
| chr4:118096659
|
GTAGATAG others(9): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.982-8322_982-8307d others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096659 | |||||
| chr4:118096668
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-8350T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096668 | ||||||
| chr4:118096708
|
T | C | 2 | a0001c0002t0001g0029a0001c0005t0001g0109 | 2 | HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.982-8310T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096708 | ||||||
| chr4:118096712
|
CAGTT | C | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.982-8303_982-8300d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118096712 | |||||
| chr4:118096746
|
T | C | 1 | a0001c0001t0008g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.982-8272T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096746 | ||||||
| chr4:118096895
|
G | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-8123G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096895 | ||||||
| chr4:118096964
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.982-8054G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118096964 | ||||||
| chr4:118097081
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.982-7937G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097081 | ||||||
| chr4:118097239
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.982-7779A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097239 | ||||||
| chr4:118097262
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.982-7756A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097262 | ||||||
| chr4:118097546
|
C | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-7472C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097546 | ||||||
| chr4:118097661
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-7357T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097661 | ||||||
| chr4:118097750
|
T | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.982-7268T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097750 | ||||||
| chr4:118097774
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.982-7244G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097774 | ||||||
| chr4:118097957
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.982-7061T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118097957 | ||||||
| chr4:118098016
|
G | C | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.982-7002G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098016 | ||||||
| chr4:118098017
|
G | T | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.982-7001G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098017 | ||||||
| chr4:118098048
|
G | GT | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.982-6962dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118098048 | |||||
| chr4:118098250
|
A | T | 1 | a0001c0003t0002g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.982-6768A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098250 | ||||||
| chr4:118098415
|
G | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.982-6603G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098415 | ||||||
| chr4:118098605
|
C | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-6413C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098605 | ||||||
| chr4:118098776
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-6242A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098776 | ||||||
| chr4:118098953
|
A | G | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-6065A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118098953 | ||||||
| chr4:118099068
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-5950T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099068 | ||||||
| chr4:118099069
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-5949A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099069 | ||||||
| chr4:118099070
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-5948T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099070 | ||||||
| chr4:118099151
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.982-5867T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099151 | ||||||
| chr4:118099297
|
G | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.982-5721G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099297 | ||||||
| chr4:118099549
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.982-5469G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099549 | ||||||
| chr4:118099693
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.982-5325G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099693 | ||||||
| chr4:118099913
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.982-5105T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118099913 | ||||||
| chr4:118101113
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.982-3905A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101113 | ||||||
| chr4:118101144
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-3874C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101144 | ||||||
| chr4:118101289
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-3729C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101289 | ||||||
| chr4:118101368
|
G | GA | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-3636dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118101368 | |||||
| chr4:118101383
|
C | T | 1 | a0001c0002t0001g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-3635C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101383 | ||||||
| chr4:118101488
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-3530C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101488 | ||||||
| chr4:118101574
|
T | C | 1 | a0001c0004t0003g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.982-3444T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101574 | ||||||
| chr4:118101577
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-3441C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118101577 | ||||||
| chr4:118102371
|
C | T | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.982-2647C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118102371 | ||||||
| chr4:118102673
|
T | C | 1 | a0001c0003t0002g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.982-2345T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118102673 | ||||||
| chr4:118102859
|
T | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.982-2159T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118102859 | ||||||
| chr4:118102973
|
G | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-2045G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118102973 | ||||||
| chr4:118103393
|
A | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.982-1625A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118103393 | ||||||
| chr4:118103440
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.982-1578T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118103440 | ||||||
| chr4:118103565
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-1453C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118103565 | ||||||
| chr4:118103692
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.982-1326C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118103692 | ||||||
| chr4:118103884
|
T | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.982-1134T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118103884 | ||||||
| chr4:118104078
|
T | C | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-940T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104078 | ||||||
| chr4:118104081
|
G | C | 50 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(47): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.982-937G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104081 | ||||||
| chr4:118104099
|
TG | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0174 | 3 | HG00544.hp1 NA18954.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.982-916delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 118104099 | |||||
| chr4:118104335
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.982-683G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104335 | ||||||
| chr4:118104609
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 47 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.982-409T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104609 | ||||||
| chr4:118104704
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0086others(41): Show | 44 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.982-314T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104704 | ||||||
| chr4:118104735
|
C | G | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.982-283C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104735 | ||||||
| chr4:118104878
|
T | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-140T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | chr4 | 118104878 | ||||||
| chr4:118105315
|
A | G | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069+210A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105315 | ||||||
| chr4:118105482
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+377G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105482 | ||||||
| chr4:118105491
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+386T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105491 | ||||||
| chr4:118105554
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+449C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105554 | ||||||
| chr4:118105597
|
T | A | 2 | a0001c0001t0001g0024a0001c0003t0002g0025 | 2 | NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1069+492T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105597 | ||||||
| chr4:118105610
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+505A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105610 | ||||||
| chr4:118105613
|
A | G | 8 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1069+508A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105613 | ||||||
| chr4:118105647
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+542C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105647 | ||||||
| chr4:118105703
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+598A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105703 | ||||||
| chr4:118105714
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1069+609G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118105714 | ||||||
| chr4:118106193
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1069+1088C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106193 | ||||||
| chr4:118106378
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1069+1273C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106378 | ||||||
| chr4:118106502
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1397T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106502 | ||||||
| chr4:118106510
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1405A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106510 | ||||||
| chr4:118106861
|
C | T | 4 | a0001c0002t0001g0084a0001c0009t0003g0065a0001c0009t0021g0067others(1): Show | 4 | HG02148.hp2 HG02602.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+1756C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106861 | ||||||
| chr4:118106871
|
G | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1069+1766G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118106871 | ||||||
| chr4:118107044
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0158 | 2 | NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1069+1939T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107044 | ||||||
| chr4:118107069
|
T | C | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069+1964T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107069 | ||||||
| chr4:118107091
|
AAAT | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(35): Show | 39 | HG00544.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1069+2005_1069+200 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107091 | |||||
| chr4:118107091
|
AAATAAT | A | 18 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG00597.hp2 HG02027.hp2 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+2002_1069+200 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107091 | |||||
| chr4:118107092
|
A | AATC | 12 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01070.hp2 HG01109.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1069+1989_1069+199 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107092 | |||||
| chr4:118107095
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1990A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107095 | ||||||
| chr4:118107098
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1993A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107098 | ||||||
| chr4:118107101
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1996A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107101 | ||||||
| chr4:118107104
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+1999A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107104 | ||||||
| chr4:118107107
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+2002A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107107 | ||||||
| chr4:118107110
|
A | AATC | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(35): Show | 39 | HG00544.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1069+2021_1069+202 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107110 | |||||
| chr4:118107110
|
A | AATCATC | 18 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG00597.hp2 HG02027.hp2 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+2018_1069+202 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107110 | |||||
| chr4:118107110
|
A | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+2005A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107110 | ||||||
| chr4:118107479
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1069+2374T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107479 | ||||||
| chr4:118107736
|
TA | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1069+2633delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118107736 | |||||
| chr4:118107805
|
T | C | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1069+2700T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107805 | ||||||
| chr4:118107816
|
C | T | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069+2711C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107816 | ||||||
| chr4:118107817
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1069+2712T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107817 | ||||||
| chr4:118107914
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1069+2809T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107914 | ||||||
| chr4:118107991
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1069+2886A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118107991 | ||||||
| chr4:118108055
|
C | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1069+2950C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108055 | ||||||
| chr4:118108077
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1069+2972T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108077 | ||||||
| chr4:118108210
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1069+3105G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108210 | ||||||
| chr4:118108429
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1069+3324T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108429 | ||||||
| chr4:118108520
|
TATC | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1069+3418_1069+342 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118108520 | |||||
| chr4:118108544
|
A | G | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069+3439A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108544 | ||||||
| chr4:118108638
|
G | A | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1069+3533G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108638 | ||||||
| chr4:118108777
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069+3672T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108777 | ||||||
| chr4:118108897
|
GAAC | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1069+3793_1069+379 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118108897 | ||||||
| chr4:118109305
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1069+4200T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109305 | ||||||
| chr4:118109315
|
G | A | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1069+4210G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109315 | ||||||
| chr4:118109440
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1069+4335T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109440 | ||||||
| chr4:118109453
|
A | G | 1 | a0001c0001t0016g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1069+4348A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109453 | ||||||
| chr4:118109532
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1069+4427C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109532 | ||||||
| chr4:118109680
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1069+4575A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118109680 | ||||||
| chr4:118110023
|
G | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1070-4783G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118110023 | ||||||
| chr4:118110502
|
T | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1070-4304T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118110502 | ||||||
| chr4:118110908
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1070-3898G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118110908 | ||||||
| chr4:118110926
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1070-3880A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118110926 | ||||||
| chr4:118111085
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1070-3721C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111085 | ||||||
| chr4:118111144
|
A | G | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1070-3662A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111144 | ||||||
| chr4:118111343
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1070-3463C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111343 | ||||||
| chr4:118111453
|
A | T | 2 | a0001c0010t0003g0171a0001c0010t0003g0213 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1070-3353A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111453 | ||||||
| chr4:118111535
|
AT | A | 11 | a0001c0001t0001g0138a0001c0004t0001g0197a0001c0004t0002g0198others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1070-3252delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118111535 | |||||
| chr4:118111535
|
ATTTT | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1070-3255_1070-325 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118111535 | |||||
| chr4:118111568
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1070-3238G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111568 | ||||||
| chr4:118111571
|
C | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1070-3235C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111571 | ||||||
| chr4:118111576
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1070-3230A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111576 | ||||||
| chr4:118111583
|
C | G | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1070-3223C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111583 | ||||||
| chr4:118111704
|
A | T | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-3102A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111704 | ||||||
| chr4:118111742
|
T | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0041others(4): Show | 7 | HG00544.hp2 HG02165.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-3064T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111742 | ||||||
| chr4:118111793
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1070-3013C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111793 | ||||||
| chr4:118111839
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1070-2967T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111839 | ||||||
| chr4:118111887
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1070-2919A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111887 | ||||||
| chr4:118111969
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1070-2837C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118111969 | ||||||
| chr4:118112018
|
G | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1070-2788G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112018 | ||||||
| chr4:118112047
|
A | G | 10 | a0001c0004t0001g0197a0001c0004t0002g0198a0001c0004t0003g0194others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070-2759A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112047 | ||||||
| chr4:118112230
|
G | A | 4 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0095others(1): Show | 4 | NA18747.hp2 NA18945.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-2576G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112230 | ||||||
| chr4:118112268
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1070-2538G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112268 | ||||||
| chr4:118112339
|
T | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1070-2467T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112339 | ||||||
| chr4:118112386
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1070-2420C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112386 | ||||||
| chr4:118112482
|
C | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1070-2324C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112482 | ||||||
| chr4:118112521
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1070-2285T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112521 | ||||||
| chr4:118112717
|
A | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1070-2089A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112717 | ||||||
| chr4:118112857
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1070-1949C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112857 | ||||||
| chr4:118112961
|
A | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0120others(6): Show | 9 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1845A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118112961 | ||||||
| chr4:118113031
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1070-1775A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118113031 | ||||||
| chr4:118113401
|
T | C | 12 | a0001c0004t0001g0197a0001c0004t0002g0198a0001c0004t0003g0194others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1070-1405T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118113401 | ||||||
| chr4:118113403
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1070-1403C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118113403 | ||||||
| chr4:118113447
|
T | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1070-1359T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118113447 | ||||||
| chr4:118113460
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1070-1346C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118113460 | ||||||
| chr4:118114189
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1070-617G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118114189 | ||||||
| chr4:118114290
|
C | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1070-516C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118114290 | ||||||
| chr4:118114682
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0212others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-124C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | chr4 | 118114682 | ||||||
| chr4:118114793
|
T | TC | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
splice_region_variant&intron_variant | LOW | c.1070-6dupC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 118114793 | |||||
| chr4:118114976
|
T | C | 8 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1224+16T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118114976 | ||||||
| chr4:118115090
|
C | T | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1224+130C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115090 | ||||||
| chr4:118115201
|
C | T | 1 | a0001c0009t0021g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1224+241C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115201 | ||||||
| chr4:118115447
|
G | A | 1 | a0001c0003t0002g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1224+487G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115447 | ||||||
| chr4:118115487
|
G | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1224+527G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115487 | ||||||
| chr4:118115671
|
C | T | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+711C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115671 | ||||||
| chr4:118115738
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0014g0110 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1224+778T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115738 | ||||||
| chr4:118115743
|
CAACT | C | 4 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(1): Show | 4 | HG02809.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+784_1224+787d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115743 | ||||||
| chr4:118115861
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1224+901A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118115861 | ||||||
| chr4:118115985
|
G | GCTC | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1224+1030_1224+103 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118115985 | |||||
| chr4:118116000
|
T | C | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1224+1040T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116000 | ||||||
| chr4:118116039
|
GAGA | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1224+1082_1224+108 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118116039 | |||||
| chr4:118116495
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1224+1535C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116495 | ||||||
| chr4:118116657
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+1697A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116657 | ||||||
| chr4:118116821
|
G | A | 7 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1224+1861G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116821 | ||||||
| chr4:118116836
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1224+1876C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116836 | ||||||
| chr4:118116837
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1224+1877G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118116837 | ||||||
| chr4:118117317
|
T | A | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1224+2357T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118117317 | ||||||
| chr4:118117485
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1224+2525G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118117485 | ||||||
| chr4:118118730
|
A | T | 7 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0133others(4): Show | 7 | HG00597.hp2 HG02027.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1224+3770A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118118730 | ||||||
| chr4:118118759
|
G | C | 2 | a0001c0005t0004g0108a0001c0017t0001g0207 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1224+3799G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118118759 | ||||||
| chr4:118118777
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1224+3817A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118118777 | ||||||
| chr4:118119100
|
T | C | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1224+4140T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118119100 | ||||||
| chr4:118119657
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1224+4697G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118119657 | ||||||
| chr4:118120198
|
A | G | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG02109.hp2 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1224+5238A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120198 | ||||||
| chr4:118120238
|
A | G | 10 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+5278A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120238 | ||||||
| chr4:118120316
|
C | T | 17 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(14): Show | 17 | HG01074.hp2 HG01109.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1224+5356C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120316 | ||||||
| chr4:118120421
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1224+5461G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120421 | ||||||
| chr4:118120639
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+5679A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120639 | ||||||
| chr4:118120804
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+5844G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120804 | ||||||
| chr4:118120994
|
C | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1224+6034C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120994 | ||||||
| chr4:118120994
|
C | T | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1224+6034C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118120994 | ||||||
| chr4:118121004
|
T | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+6044T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121004 | ||||||
| chr4:118121061
|
C | T | 8 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1224+6101C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121061 | ||||||
| chr4:118121125
|
T | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+6165T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121125 | ||||||
| chr4:118121215
|
A | C | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1224+6255A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121215 | ||||||
| chr4:118121286
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1224+6326T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121286 | ||||||
| chr4:118121460
|
T | G | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1224+6500T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121460 | ||||||
| chr4:118121578
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1224+6618C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121578 | ||||||
| chr4:118121623
|
G | T | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+6663G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121623 | ||||||
| chr4:118121658
|
T | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1224+6698T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121658 | ||||||
| chr4:118121684
|
GC | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 80 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1224+6725delC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121684 | ||||||
| chr4:118121702
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1224+6742T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118121702 | ||||||
| chr4:118122084
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1224+7124G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122084 | ||||||
| chr4:118122191
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1224+7231T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122191 | ||||||
| chr4:118122298
|
T | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224+7338T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122298 | ||||||
| chr4:118122313
|
T | A | 13 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1224+7353T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122313 | ||||||
| chr4:118122325
|
G | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1224+7365G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122325 | ||||||
| chr4:118122367
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1224+7407G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122367 | ||||||
| chr4:118122428
|
C | T | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1224+7468C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122428 | ||||||
| chr4:118122493
|
TC | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1224+7534delC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122493 | ||||||
| chr4:118122494
|
C | T | 7 | a0001c0001t0020g0113a0001c0002t0001g0098a0001c0005t0001g0107others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1224+7534C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122494 | ||||||
| chr4:118122695
|
G | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1224+7735G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122695 | ||||||
| chr4:118122806
|
C | T | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1224+7846C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122806 | ||||||
| chr4:118122933
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1224+7973T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118122933 | ||||||
| chr4:118123268
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1224+8308A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123268 | ||||||
| chr4:118123504
|
C | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1224+8544C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123504 | ||||||
| chr4:118123637
|
A | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1224+8677A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123637 | ||||||
| chr4:118123764
|
G | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1224+8804G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123764 | ||||||
| chr4:118123888
|
T | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0096 | 2 | NA18747.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1224+8928T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123888 | ||||||
| chr4:118123984
|
G | A | 9 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1224+9024G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118123984 | ||||||
| chr4:118124493
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+9533G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118124493 | ||||||
| chr4:118124544
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1224+9584G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118124544 | ||||||
| chr4:118124729
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0165 | 3 | HG01433.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1224+9769T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118124729 | ||||||
| chr4:118124737
|
T | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1224+9777T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118124737 | ||||||
| chr4:118124745
|
C | G | 1 | a0001c0003t0002g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1224+9785C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118124745 | ||||||
| chr4:118125017
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 84 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1224+10057A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125017 | ||||||
| chr4:118125179
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1224+10219T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125179 | ||||||
| chr4:118125198
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1224+10238A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125198 | ||||||
| chr4:118125208
|
A | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1224+10248A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125208 | ||||||
| chr4:118125574
|
G | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+10614G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125574 | ||||||
| chr4:118125613
|
C | T | 2 | a0001c0003t0002g0034a0001c0003t0002g0063 | 2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1224+10653C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125613 | ||||||
| chr4:118125674
|
C | T | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1224+10714C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125674 | ||||||
| chr4:118125726
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1224+10766C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125726 | ||||||
| chr4:118125843
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1224+10883C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118125843 | ||||||
| chr4:118126040
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1224+11080A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126040 | ||||||
| chr4:118126119
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1224+11159A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126119 | ||||||
| chr4:118126139
|
G | A | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1224+11179G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126139 | ||||||
| chr4:118126347
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1224+11387T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126347 | ||||||
| chr4:118126437
|
G | A | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+11477G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126437 | ||||||
| chr4:118126514
|
GTATATAT others(17): Show |
G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1225-11523_1225-11 others(30): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126514 | |||||
| chr4:118126515
|
TATATATA others(15): Show |
T | 51 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(48): Show | 51 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1225-11521_1225-11 others(28): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126515 | |||||
| chr4:118126519
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1225-11519_1225-11 others(24): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126519 | |||||
| chr4:118126521
|
TATATATA others(9): Show |
T | 72 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1225-11519_1225-11 others(22): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126521 | |||||
| chr4:118126523
|
T | TATATATA others(35): Show |
1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-11520_1225-11 others(48): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126523 | |||||
| chr4:118126523
|
TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0003t0002g0025 | 3 | HG03688.hp1 NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1225-11519_1225-11 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126523 | |||||
| chr4:118126525
|
TATATATA others(5): Show |
T | 3 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0108 | 3 | HG02615.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1225-11519_1225-11 others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126525 | |||||
| chr4:118126527
|
TATATATA others(3): Show |
T | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1225-11519_1225-11 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126527 | |||||
| chr4:118126533
|
T | C | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1225-11521T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126533 | ||||||
| chr4:118126535
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-11519C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126535 | ||||||
| chr4:118126537
|
C | CATATATA others(15): Show |
5 | a0001c0006t0001g0103a0001c0007t0001g0200a0001c0007t0001g0201others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-11504_1225-11 others(28): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126537 | |||||
| chr4:118126537
|
C | CATATATA others(21): Show |
1 | a0001c0006t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1225-11504_1225-11 others(34): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126537 | |||||
| chr4:118126537
|
C | CATATATA others(17): Show |
6 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1225-11502_1225-11 others(30): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118126537 | |||||
| chr4:118126537
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-11517C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126537 | ||||||
| chr4:118126539
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1225-11515T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126539 | ||||||
| chr4:118126567
|
T | C | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1225-11487T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126567 | ||||||
| chr4:118126755
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1225-11299T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126755 | ||||||
| chr4:118126777
|
C | A | 1 | a0001c0004t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1225-11277C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126777 | ||||||
| chr4:118126814
|
C | T | 1 | a0001c0003t0002g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1225-11240C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126814 | ||||||
| chr4:118126901
|
T | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1225-11153T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118126901 | ||||||
| chr4:118127160
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1225-10894T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127160 | ||||||
| chr4:118127166
|
T | C | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1225-10888T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127166 | ||||||
| chr4:118127230
|
G | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1225-10824G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127230 | ||||||
| chr4:118127391
|
G | C | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1225-10663G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127391 | ||||||
| chr4:118127437
|
G | T | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1225-10617G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127437 | ||||||
| chr4:118127505
|
A | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1225-10549A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127505 | ||||||
| chr4:118127524
|
G | T | 1 | a0001c0001t0001g0146 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1225-10530G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127524 | ||||||
| chr4:118127627
|
A | T | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-10427A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118127627 | ||||||
| chr4:118128011
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1225-10043T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128011 | ||||||
| chr4:118128064
|
T | A | 1 | a0001c0003t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1225-9990T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128064 | ||||||
| chr4:118128095
|
A | G | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1225-9959A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128095 | ||||||
| chr4:118128356
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1225-9698A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128356 | ||||||
| chr4:118128448
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1225-9606T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128448 | ||||||
| chr4:118128643
|
T | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1225-9411T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128643 | ||||||
| chr4:118128676
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1225-9378G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128676 | ||||||
| chr4:118128709
|
C | G | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-9345C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128709 | ||||||
| chr4:118128812
|
G | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1225-9242G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128812 | ||||||
| chr4:118128975
|
T | G | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1225-9079T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118128975 | ||||||
| chr4:118129178
|
A | G | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1225-8876A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129178 | ||||||
| chr4:118129269
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1225-8785G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129269 | ||||||
| chr4:118129298
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1225-8756T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129298 | ||||||
| chr4:118129343
|
G | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1225-8711G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129343 | ||||||
| chr4:118129771
|
C | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1225-8283C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129771 | ||||||
| chr4:118129836
|
A | C | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1225-8218A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129836 | ||||||
| chr4:118129909
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1225-8145C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118129909 | ||||||
| chr4:118130032
|
A | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 82 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1225-8022A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130032 | ||||||
| chr4:118130098
|
T | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-7956T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130098 | ||||||
| chr4:118130111
|
ATCATAGA others(3): Show |
A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1225-7941_1225-793 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118130111 | |||||
| chr4:118130137
|
T | C | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-7917T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130137 | ||||||
| chr4:118130144
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1225-7910A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130144 | ||||||
| chr4:118130226
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1225-7828T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130226 | ||||||
| chr4:118130255
|
C | T | 31 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(28): Show | 31 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1225-7799C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130255 | ||||||
| chr4:118130429
|
C | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-7625C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130429 | ||||||
| chr4:118130680
|
A | T | 9 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-7374A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130680 | ||||||
| chr4:118130953
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-7101C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118130953 | ||||||
| chr4:118131254
|
T | TTTTGG | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-6771_1225-676 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118131254 | |||||
| chr4:118131254
|
TTTTGG | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1225-6771_1225-676 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118131254 | |||||
| chr4:118131254
|
TTTTGGTT others(3): Show |
T | 2 | a0001c0001t0001g0150a0001c0001t0001g0165 | 2 | HG01433.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1225-6776_1225-676 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118131254 | |||||
| chr4:118131276
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18972.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1225-6778T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131276 | ||||||
| chr4:118131411
|
A | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1225-6643A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131411 | ||||||
| chr4:118131634
|
C | A | 6 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(3): Show | 6 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-6420C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131634 | ||||||
| chr4:118131740
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1225-6314A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131740 | ||||||
| chr4:118131748
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1225-6306T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131748 | ||||||
| chr4:118131875
|
C | A | 1 | a0001c0003t0002g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1225-6179C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118131875 | ||||||
| chr4:118132212
|
G | A | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1225-5842G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132212 | ||||||
| chr4:118132236
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1225-5818G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132236 | ||||||
| chr4:118132382
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1225-5672G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132382 | ||||||
| chr4:118132555
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225-5499C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132555 | ||||||
| chr4:118132814
|
A | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0185others(1): Show | 4 | HG00099.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-5240A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132814 | ||||||
| chr4:118132923
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1225-5131C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132923 | ||||||
| chr4:118132945
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1225-5109C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118132945 | ||||||
| chr4:118133013
|
G | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1225-5041G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133013 | ||||||
| chr4:118133052
|
C | G | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-5002C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133052 | ||||||
| chr4:118133118
|
A | G | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-4936A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133118 | ||||||
| chr4:118133223
|
A | C | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-4831A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133223 | ||||||
| chr4:118133527
|
G | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-4527G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133527 | ||||||
| chr4:118133633
|
G | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1225-4421G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133633 | ||||||
| chr4:118133713
|
G | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-4341G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133713 | ||||||
| chr4:118133728
|
C | G | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1225-4326C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133728 | ||||||
| chr4:118133739
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0014g0110 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1225-4315C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133739 | ||||||
| chr4:118133921
|
C | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1225-4133C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133921 | ||||||
| chr4:118133926
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1225-4128T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118133926 | ||||||
| chr4:118134256
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225-3798C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134256 | ||||||
| chr4:118134257
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1225-3797A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134257 | ||||||
| chr4:118134284
|
G | A | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1225-3770G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134284 | ||||||
| chr4:118134297
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1225-3757C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134297 | ||||||
| chr4:118134298
|
G | A | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1225-3756G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134298 | ||||||
| chr4:118134414
|
T | C | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1225-3640T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134414 | ||||||
| chr4:118134443
|
C | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-3611C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134443 | ||||||
| chr4:118134471
|
AG | A | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-3582delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134471 | ||||||
| chr4:118134524
|
T | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-3530T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134524 | ||||||
| chr4:118134680
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1225-3374A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134680 | ||||||
| chr4:118134770
|
C | T | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-3284C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134770 | ||||||
| chr4:118134804
|
T | C | 5 | a0001c0004t0003g0196a0001c0004t0003g0205a0001c0004t0019g0195others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-3250T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134804 | ||||||
| chr4:118134887
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225-3167C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118134887 | ||||||
| chr4:118135048
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1225-3006G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135048 | ||||||
| chr4:118135117
|
A | G | 3 | a0001c0004t0003g0196a0001c0004t0003g0205a0001c0018t0003g0071 | 3 | HG02109.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1225-2937A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135117 | ||||||
| chr4:118135531
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0212others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-2523C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135531 | ||||||
| chr4:118135532
|
T | C | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1225-2522T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135532 | ||||||
| chr4:118135659
|
G | A | 1 | a0001c0003t0002g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1225-2395G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135659 | ||||||
| chr4:118135783
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1225-2271C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118135783 | ||||||
| chr4:118135862
|
G | GT | 8 | a0001c0001t0001g0024a0001c0003t0002g0012a0001c0003t0002g0020others(5): Show | 8 | HG02027.hp1 HG02148.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1225-2191dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118135862 | |||||
| chr4:118136165
|
C | T | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1225-1889C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136165 | ||||||
| chr4:118136352
|
G | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1702G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136352 | ||||||
| chr4:118136425
|
A | C | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1225-1629A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136425 | ||||||
| chr4:118136467
|
ATTAGT | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1225-1579_1225-157 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118136467 | |||||
| chr4:118136468
|
T | C | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1586T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136468 | ||||||
| chr4:118136471
|
G | C | 18 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1225-1583G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136471 | ||||||
| chr4:118136499
|
C | T | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1225-1555C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136499 | ||||||
| chr4:118136822
|
A | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1225-1232A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118136822 | ||||||
| chr4:118137311
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1225-743C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118137311 | ||||||
| chr4:118137347
|
G | GC | 9 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-705dupC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 118137347 | |||||
| chr4:118137734
|
G | A | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-320G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118137734 | ||||||
| chr4:118137936
|
A | G | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1225-118A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 4/13 | chr4 | 118137936 | ||||||
| chr4:118138408
|
C | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0178 | 2 | NA18970.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1410+169C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118138408 | ||||||
| chr4:118138515
|
G | C | 1 | a0001c0003t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1410+276G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118138515 | ||||||
| chr4:118139027
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1410+788T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139027 | ||||||
| chr4:118139176
|
C | T | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+937C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139176 | ||||||
| chr4:118139381
|
A | G | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+1142A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139381 | ||||||
| chr4:118139397
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1410+1158G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139397 | ||||||
| chr4:118139399
|
A | G | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1410+1160A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139399 | ||||||
| chr4:118139683
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1410+1444C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139683 | ||||||
| chr4:118139780
|
T | C | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1410+1541T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139780 | ||||||
| chr4:118139783
|
C | G | 1 | a0001c0001t0001g0050 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1410+1544C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139783 | ||||||
| chr4:118139866
|
T | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1410+1627T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118139866 | ||||||
| chr4:118140007
|
C | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1410+1768C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140007 | ||||||
| chr4:118140090
|
C | T | 4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+1851C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140090 | ||||||
| chr4:118140302
|
C | T | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1410+2063C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140302 | ||||||
| chr4:118140550
|
T | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1410+2311T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140550 | ||||||
| chr4:118140565
|
A | G | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1410+2326A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140565 | ||||||
| chr4:118140573
|
G | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1410+2334G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140573 | ||||||
| chr4:118140646
|
A | G | 1 | a0001c0003t0002g0025 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1410+2407A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140646 | ||||||
| chr4:118140673
|
A | G | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1410+2434A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140673 | ||||||
| chr4:118140785
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+2546C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140785 | ||||||
| chr4:118140856
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1410+2617C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140856 | ||||||
| chr4:118140982
|
A | G | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411-2574A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118140982 | ||||||
| chr4:118141065
|
G | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1411-2491G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141065 | ||||||
| chr4:118141254
|
G | C | 13 | a0001c0001t0001g0184a0001c0002t0001g0061a0001c0002t0001g0088others(10): Show | 13 | HG00597.hp1 NA18747.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411-2302G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141254 | ||||||
| chr4:118141298
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411-2258G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141298 | ||||||
| chr4:118141303
|
A | AT | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411-2252dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 118141303 | |||||
| chr4:118141375
|
T | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1411-2181T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141375 | ||||||
| chr4:118141381
|
T | G | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1411-2175T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141381 | ||||||
| chr4:118141434
|
G | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1411-2122G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141434 | ||||||
| chr4:118141495
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411-2061A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141495 | ||||||
| chr4:118141498
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1411-2058G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141498 | ||||||
| chr4:118141564
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1411-1992C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141564 | ||||||
| chr4:118141668
|
A | C | 1 | a0001c0005t0004g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411-1888A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118141668 | ||||||
| chr4:118142034
|
A | T | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1411-1522A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142034 | ||||||
| chr4:118142066
|
T | A | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411-1490T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142066 | ||||||
| chr4:118142190
|
C | T | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1411-1366C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142190 | ||||||
| chr4:118142299
|
T | C | 14 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1411-1257T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142299 | ||||||
| chr4:118142445
|
A | T | 1 | a0001c0002t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1411-1111A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142445 | ||||||
| chr4:118142446
|
T | A | 1 | a0001c0002t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1411-1110T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142446 | ||||||
| chr4:118142475
|
AAAAACAC others(8): Show |
A | 1 | a0001c0002t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1411-1080_1411-106 others(19): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142475 | ||||||
| chr4:118142644
|
A | G | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1411-912A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142644 | ||||||
| chr4:118142826
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1411-730C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142826 | ||||||
| chr4:118142856
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(211): Show |
intron_variant | MODIFIER | c.1411-700C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142856 | ||||||
| chr4:118142860
|
T | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1411-696T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142860 | ||||||
| chr4:118142883
|
C | A | 1 | a0001c0011t0009g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1411-673C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118142883 | ||||||
| chr4:118143102
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1411-454T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118143102 | ||||||
| chr4:118143237
|
CT | C | 5 | a0001c0002t0001g0090a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-310delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 118143237 | |||||
| chr4:118143438
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1411-118G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118143438 | ||||||
| chr4:118143513
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1411-43G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 5/13 | chr4 | 118143513 | ||||||
| chr4:118143952
|
T | C | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+268T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118143952 | ||||||
| chr4:118143994
|
C | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+310C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118143994 | ||||||
| chr4:118144003
|
A | AT | 56 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(53): Show | 56 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1539+328dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118144003 | |||||
| chr4:118144186
|
C | CT | 14 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1539+514dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118144186 | |||||
| chr4:118144221
|
C | A | 2 | a0001c0002t0001g0170a0001c0002t0001g0182 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1539+537C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144221 | ||||||
| chr4:118144238
|
T | G | 1 | a0001c0003t0002g0016 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1539+554T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144238 | ||||||
| chr4:118144288
|
C | T | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+604C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144288 | ||||||
| chr4:118144300
|
C | G | 1 | a0001c0002t0001g0172 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1539+616C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144300 | ||||||
| chr4:118144330
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1539+646G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144330 | ||||||
| chr4:118144340
|
G | C | 14 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1539+656G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144340 | ||||||
| chr4:118144419
|
A | T | 14 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1539+735A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144419 | ||||||
| chr4:118144460
|
G | A | 4 | a0001c0001t0018g0162a0001c0003t0002g0152a0001c0004t0001g0199others(1): Show | 4 | HG02486.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+776G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144460 | ||||||
| chr4:118144539
|
T | A | 14 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1539+855T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144539 | ||||||
| chr4:118144563
|
GA | G | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+882delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118144563 | |||||
| chr4:118144709
|
T | C | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1539+1025T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118144709 | ||||||
| chr4:118144745
|
TA | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1539+1073delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118144745 | |||||
| chr4:118145018
|
G | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+1334G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145018 | ||||||
| chr4:118145088
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+1404T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145088 | ||||||
| chr4:118145516
|
G | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+1832G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145516 | ||||||
| chr4:118145680
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1539+1996T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145680 | ||||||
| chr4:118145893
|
T | C | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+2209T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145893 | ||||||
| chr4:118145898
|
C | T | 18 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+2214C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145898 | ||||||
| chr4:118145932
|
T | G | 7 | a0001c0001t0001g0037a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | NA18945.hp2 NA18956.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+2248T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118145932 | ||||||
| chr4:118146194
|
T | C | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+2510T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146194 | ||||||
| chr4:118146217
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+2533A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146217 | ||||||
| chr4:118146263
|
A | C | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+2579A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146263 | ||||||
| chr4:118146308
|
G | A | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+2624G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146308 | ||||||
| chr4:118146357
|
C | T | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+2673C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146357 | ||||||
| chr4:118146397
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1539+2713C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146397 | ||||||
| chr4:118146398
|
A | G | 64 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(61): Show | 64 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1539+2714A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146398 | ||||||
| chr4:118146468
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+2784G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146468 | ||||||
| chr4:118146524
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1539+2840G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146524 | ||||||
| chr4:118146553
|
T | TA | 6 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(3): Show | 6 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+2876dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118146553 | |||||
| chr4:118146585
|
C | T | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+2901C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146585 | ||||||
| chr4:118146712
|
G | A | 5 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+3028G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146712 | ||||||
| chr4:118146937
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+3253G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118146937 | ||||||
| chr4:118147285
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1539+3601G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118147285 | ||||||
| chr4:118147482
|
T | G | 65 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(62): Show | 65 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1539+3798T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118147482 | ||||||
| chr4:118147736
|
C | T | 19 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.1539+4052C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118147736 | ||||||
| chr4:118148019
|
C | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+4335C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148019 | ||||||
| chr4:118148037
|
G | A | 7 | a0001c0001t0001g0163a0001c0001t0020g0113a0001c0005t0001g0107others(4): Show | 7 | HG01978.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+4353G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148037 | ||||||
| chr4:118148039
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+4355C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148039 | ||||||
| chr4:118148115
|
G | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+4431G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148115 | ||||||
| chr4:118148359
|
T | C | 7 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+4675T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148359 | ||||||
| chr4:118148389
|
C | T | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1539+4705C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148389 | ||||||
| chr4:118148409
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1539+4725C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148409 | ||||||
| chr4:118148520
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1539+4836C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148520 | ||||||
| chr4:118148714
|
G | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+5030G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148714 | ||||||
| chr4:118148807
|
G | A | 1 | a0001c0001t0015g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1539+5123G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148807 | ||||||
| chr4:118148900
|
A | C | 1 | a0001c0001t0001g0001 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1539+5216A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118148900 | ||||||
| chr4:118149019
|
C | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+5335C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149019 | ||||||
| chr4:118149032
|
T | A | 1 | a0001c0001t0001g0159 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1539+5348T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149032 | ||||||
| chr4:118149044
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1539+5360T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149044 | ||||||
| chr4:118149121
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0054 | 2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1539+5437T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149121 | ||||||
| chr4:118149193
|
C | T | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1539+5509C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149193 | ||||||
| chr4:118149430
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1539+5746T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149430 | ||||||
| chr4:118149492
|
G | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+5808G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149492 | ||||||
| chr4:118149498
|
T | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+5814T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149498 | ||||||
| chr4:118149558
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0176 | 2 | HG01975.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1539+5874T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149558 | ||||||
| chr4:118149584
|
G | C | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1539+5900G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149584 | ||||||
| chr4:118149655
|
G | A | 1 | a0001c0008t0003g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1539+5971G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149655 | ||||||
| chr4:118149697
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1539+6013G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149697 | ||||||
| chr4:118149732
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1539+6048T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149732 | ||||||
| chr4:118149948
|
G | A | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1539+6264G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149948 | ||||||
| chr4:118149963
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+6279G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118149963 | ||||||
| chr4:118149965
|
AG | A | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+6284delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118149965 | |||||
| chr4:118150107
|
C | T | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+6423C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150107 | ||||||
| chr4:118150109
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1539+6425C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150109 | ||||||
| chr4:118150168
|
T | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+6484T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150168 | ||||||
| chr4:118150240
|
G | A | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1539+6556G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150240 | ||||||
| chr4:118150371
|
A | C | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1539+6687A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150371 | ||||||
| chr4:118150429
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+6745T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150429 | ||||||
| chr4:118150570
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+6886G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150570 | ||||||
| chr4:118150572
|
C | T | 2 | a0001c0004t0001g0197a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1539+6888C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150572 | ||||||
| chr4:118150573
|
G | A | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0013g0119others(7): Show | 10 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+6889G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150573 | ||||||
| chr4:118150623
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18972.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1539+6939A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150623 | ||||||
| chr4:118150646
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0193 | 3 | HG01361.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1539+6962T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150646 | ||||||
| chr4:118150711
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7027A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150711 | ||||||
| chr4:118150715
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7031A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150715 | ||||||
| chr4:118150721
|
C | A | 17 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1539+7037C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150721 | ||||||
| chr4:118150765
|
A | T | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7081A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150765 | ||||||
| chr4:118150775
|
T | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7091T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150775 | ||||||
| chr4:118150823
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7139G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150823 | ||||||
| chr4:118150830
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7146A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150830 | ||||||
| chr4:118150839
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7155A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150839 | ||||||
| chr4:118150850
|
G | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+7166G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150850 | ||||||
| chr4:118150877
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1539+7193C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150877 | ||||||
| chr4:118150947
|
T | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7263T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150947 | ||||||
| chr4:118150950
|
C | T | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7266C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150950 | ||||||
| chr4:118150951
|
A | G | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7267A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150951 | ||||||
| chr4:118150954
|
A | T | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7270A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150954 | ||||||
| chr4:118150955
|
T | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7271T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150955 | ||||||
| chr4:118150957
|
A | G | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7273A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118150957 | ||||||
| chr4:118151051
|
G | T | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+7367G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151051 | ||||||
| chr4:118151069
|
G | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+7385G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151069 | ||||||
| chr4:118151336
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1539+7652A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151336 | ||||||
| chr4:118151413
|
AAAC | A | 8 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(5): Show | 8 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1539+7744_1539+774 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118151413 | |||||
| chr4:118151707
|
G | A | 66 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(63): Show | 66 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1539+8023G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151707 | ||||||
| chr4:118151888
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+8204C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151888 | ||||||
| chr4:118151889
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0020g0113a0001c0005t0001g0107others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+8205G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151889 | ||||||
| chr4:118151945
|
T | C | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1539+8261T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151945 | ||||||
| chr4:118151968
|
G | A | 1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1539+8284G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118151968 | ||||||
| chr4:118152138
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+8454G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152138 | ||||||
| chr4:118152171
|
A | C | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1539+8487A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152171 | ||||||
| chr4:118152415
|
A | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+8731A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152415 | ||||||
| chr4:118152417
|
A | T | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+8733A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152417 | ||||||
| chr4:118152477
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+8793T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152477 | ||||||
| chr4:118152554
|
G | T | 1 | a0001c0005t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1539+8870G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152554 | ||||||
| chr4:118152772
|
G | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+9088G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152772 | ||||||
| chr4:118152992
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+9308C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118152992 | ||||||
| chr4:118153266
|
C | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+9582C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153266 | ||||||
| chr4:118153304
|
T | A | 1 | a0001c0003t0002g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1539+9620T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153304 | ||||||
| chr4:118153349
|
A | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1539+9665A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153349 | ||||||
| chr4:118153533
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+9849A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153533 | ||||||
| chr4:118153561
|
G | A | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+9877G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153561 | ||||||
| chr4:118153572
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+9888C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153572 | ||||||
| chr4:118153681
|
G | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1539+9997G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153681 | ||||||
| chr4:118153772
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+10088C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153772 | ||||||
| chr4:118153775
|
A | T | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+10091A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153775 | ||||||
| chr4:118153779
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+10095G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153779 | ||||||
| chr4:118153819
|
A | G | 65 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0002others(62): Show | 65 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1539+10135A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118153819 | ||||||
| chr4:118154023
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+10339T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154023 | ||||||
| chr4:118154254
|
C | G | 2 | a0001c0010t0003g0171a0001c0010t0003g0213 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1539+10570C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154254 | ||||||
| chr4:118154275
|
T | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+10591T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154275 | ||||||
| chr4:118154652
|
G | C | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+10968G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154652 | ||||||
| chr4:118154744
|
C | T | 6 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(3): Show | 6 | HG02109.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1539+11060C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154744 | ||||||
| chr4:118154781
|
A | G | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+11097A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154781 | ||||||
| chr4:118154790
|
G | A | 4 | a0001c0001t0017g0036a0001c0009t0003g0065a0001c0009t0021g0067others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+11106G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118154790 | ||||||
| chr4:118155055
|
C | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+11371C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118155055 | ||||||
| chr4:118155101
|
G | T | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+11417G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118155101 | ||||||
| chr4:118155594
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1539+11910A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118155594 | ||||||
| chr4:118156007
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1539+12323A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156007 | ||||||
| chr4:118156183
|
T | C | 2 | a0001c0005t0001g0109a0001c0006t0001g0066 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1539+12499T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156183 | ||||||
| chr4:118156271
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+12587C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156271 | ||||||
| chr4:118156371
|
T | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+12687T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156371 | ||||||
| chr4:118156617
|
T | G | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+12933T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156617 | ||||||
| chr4:118156637
|
T | TG | 15 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1539+12955dupG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118156637 | |||||
| chr4:118156639
|
G | GC | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+12955_1539+12 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156639 | ||||||
| chr4:118156935
|
C | A | 2 | a0001c0002t0001g0170a0001c0002t0001g0182 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1539+13251C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156935 | ||||||
| chr4:118156965
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+13281C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118156965 | ||||||
| chr4:118157027
|
C | T | 13 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+13343C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157027 | ||||||
| chr4:118157099
|
T | C | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+13415T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157099 | ||||||
| chr4:118157157
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.1539+13473A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157157 | ||||||
| chr4:118157172
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1539+13488C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157172 | ||||||
| chr4:118157230
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+13546G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157230 | ||||||
| chr4:118157250
|
C | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+13566C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157250 | ||||||
| chr4:118157315
|
A | T | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1539+13631A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157315 | ||||||
| chr4:118157428
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1539+13744G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157428 | ||||||
| chr4:118157428
|
GT | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1539+13759delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118157428 | |||||
| chr4:118157508
|
C | T | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1539+13824C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157508 | ||||||
| chr4:118157701
|
C | A | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+14017C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157701 | ||||||
| chr4:118157795
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1539+14111T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157795 | ||||||
| chr4:118157960
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1539+14276T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118157960 | ||||||
| chr4:118158278
|
G | C | 1 | a0001c0002t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1539+14594G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158278 | ||||||
| chr4:118158421
|
G | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1539+14737G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158421 | ||||||
| chr4:118158449
|
A | G | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+14765A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158449 | ||||||
| chr4:118158484
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+14800A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158484 | ||||||
| chr4:118158627
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1539+14943T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158627 | ||||||
| chr4:118158727
|
C | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+15043C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158727 | ||||||
| chr4:118158776
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1539+15092G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158776 | ||||||
| chr4:118158777
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1539+15093C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118158777 | ||||||
| chr4:118159097
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1539+15413C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159097 | ||||||
| chr4:118159174
|
C | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+15490C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159174 | ||||||
| chr4:118159224
|
T | C | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+15540T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159224 | ||||||
| chr4:118159436
|
T | C | 1 | a0001c0001t0010g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1539+15752T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159436 | ||||||
| chr4:118159462
|
C | G | 63 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(60): Show | 63 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1539+15778C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159462 | ||||||
| chr4:118159484
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+15800G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159484 | ||||||
| chr4:118159626
|
C | T | 40 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1539+15942C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159626 | ||||||
| chr4:118159755
|
A | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18984.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1539+16071A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118159755 | ||||||
| chr4:118160033
|
G | T | 1 | a0001c0003t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1539+16349G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160033 | ||||||
| chr4:118160439
|
T | C | 70 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(67): Show | 70 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1539+16755T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160439 | ||||||
| chr4:118160469
|
G | GA | 13 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0050others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1539+16797dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118160469 | |||||
| chr4:118160469
|
GA | G | 42 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1539+16797delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118160469 | |||||
| chr4:118160566
|
A | G | 1 | a0001c0012t0002g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1539+16882A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160566 | ||||||
| chr4:118160602
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1539+16918C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160602 | ||||||
| chr4:118160646
|
C | T | 25 | a0001c0001t0001g0057a0001c0001t0020g0113a0001c0004t0003g0194others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1539+16962C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160646 | ||||||
| chr4:118160690
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1539+17006G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160690 | ||||||
| chr4:118160832
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1539+17148G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160832 | ||||||
| chr4:118160846
|
G | A | 13 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+17162G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160846 | ||||||
| chr4:118160887
|
G | A | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+17203G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160887 | ||||||
| chr4:118160921
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1539+17237A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160921 | ||||||
| chr4:118160942
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+17258T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118160942 | ||||||
| chr4:118161116
|
G | A | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+17432G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161116 | ||||||
| chr4:118161120
|
T | C | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+17436T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161120 | ||||||
| chr4:118161143
|
C | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+17459C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161143 | ||||||
| chr4:118161149
|
T | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+17465T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161149 | ||||||
| chr4:118161167
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0147 | 3 | HG01256.hp1 HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1539+17483G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161167 | ||||||
| chr4:118161219
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1539+17535A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161219 | ||||||
| chr4:118161253
|
G | A | 13 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+17569G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161253 | ||||||
| chr4:118161348
|
A | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+17664A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161348 | ||||||
| chr4:118161406
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1539+17722C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161406 | ||||||
| chr4:118161465
|
G | A | 7 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0133others(4): Show | 7 | HG00597.hp2 HG02027.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+17781G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161465 | ||||||
| chr4:118161477
|
G | T | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+17793G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161477 | ||||||
| chr4:118161499
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+17815C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161499 | ||||||
| chr4:118161571
|
C | A | 2 | a0001c0002t0001g0064a0001c0002t0001g0077 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1539+17887C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161571 | ||||||
| chr4:118161577
|
T | C | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+17893T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161577 | ||||||
| chr4:118161598
|
C | T | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+17914C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161598 | ||||||
| chr4:118161729
|
T | C | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+18045T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161729 | ||||||
| chr4:118161795
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1539+18111A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161795 | ||||||
| chr4:118161826
|
G | A | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+18142G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161826 | ||||||
| chr4:118161836
|
A | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+18152A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161836 | ||||||
| chr4:118161858
|
A | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+18174A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161858 | ||||||
| chr4:118161888
|
G | A | 1 | a0001c0004t0003g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1539+18204G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161888 | ||||||
| chr4:118161893
|
C | T | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+18209C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161893 | ||||||
| chr4:118161952
|
C | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+18268C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161952 | ||||||
| chr4:118161962
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1539+18278A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161962 | ||||||
| chr4:118161970
|
C | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0193 | 3 | HG01361.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1539+18286C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161970 | ||||||
| chr4:118161986
|
C | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1539+18302C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161986 | ||||||
| chr4:118161987
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1539+18303C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161987 | ||||||
| chr4:118161993
|
T | A | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1539+18309T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161993 | ||||||
| chr4:118161997
|
C | T | 27 | a0001c0001t0001g0024a0001c0003t0002g0007a0001c0003t0002g0008others(24): Show | 27 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1539+18313C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118161997 | ||||||
| chr4:118162088
|
G | A | 2 | a0001c0003t0002g0026a0001c0003t0006g0023 | 2 | HG02602.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1539+18404G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162088 | ||||||
| chr4:118162283
|
T | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+18599T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162283 | ||||||
| chr4:118162447
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 96 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1539+18763G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162447 | ||||||
| chr4:118162462
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1539+18778T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162462 | ||||||
| chr4:118162466
|
C | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+18782C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162466 | ||||||
| chr4:118162472
|
A | C | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+18788A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162472 | ||||||
| chr4:118162509
|
T | C | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1539+18825T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162509 | ||||||
| chr4:118162523
|
G | C | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+18839G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162523 | ||||||
| chr4:118162524
|
T | G | 39 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1539+18840T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162524 | ||||||
| chr4:118162735
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1539+19051A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162735 | ||||||
| chr4:118162766
|
A | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+19082A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162766 | ||||||
| chr4:118162803
|
G | A | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+19119G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162803 | ||||||
| chr4:118162821
|
A | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+19137A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162821 | ||||||
| chr4:118162934
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+19250G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118162934 | ||||||
| chr4:118163079
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1539+19395G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163079 | ||||||
| chr4:118163194
|
A | G | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+19510A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163194 | ||||||
| chr4:118163302
|
A | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+19618A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163302 | ||||||
| chr4:118163329
|
T | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+19645T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163329 | ||||||
| chr4:118163362
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0101others(1): Show | 4 | NA18941.hp2 NA18946.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+19678T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163362 | ||||||
| chr4:118163459
|
G | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0101others(1): Show | 4 | NA18941.hp2 NA18946.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+19775G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163459 | ||||||
| chr4:118163495
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+19811G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163495 | ||||||
| chr4:118163591
|
G | T | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+19907G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163591 | ||||||
| chr4:118163608
|
G | A | 19 | a0001c0001t0001g0181a0001c0004t0003g0194a0001c0004t0003g0196others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1539+19924G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163608 | ||||||
| chr4:118163723
|
A | C | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+20039A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163723 | ||||||
| chr4:118163953
|
C | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1539+20269C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163953 | ||||||
| chr4:118163963
|
G | A | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+20279G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118163963 | ||||||
| chr4:118164001
|
A | G | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+20317A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164001 | ||||||
| chr4:118164066
|
T | C | 66 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(63): Show | 66 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1539+20382T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164066 | ||||||
| chr4:118164129
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+20445G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164129 | ||||||
| chr4:118164258
|
C | T | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+20574C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164258 | ||||||
| chr4:118164411
|
T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1539+20727T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164411 | ||||||
| chr4:118164475
|
T | TGTAA | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+20792_1539+20 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118164475 | |||||
| chr4:118164559
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+20875G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164559 | ||||||
| chr4:118164600
|
T | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+20916T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164600 | ||||||
| chr4:118164764
|
A | G | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1539+21080A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164764 | ||||||
| chr4:118164783
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+21099A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118164783 | ||||||
| chr4:118165123
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+21439A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165123 | ||||||
| chr4:118165158
|
G | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1539+21474G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165158 | ||||||
| chr4:118165416
|
CA | C | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1539+21735delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118165416 | |||||
| chr4:118165463
|
G | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+21779G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165463 | ||||||
| chr4:118165524
|
A | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+21840A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165524 | ||||||
| chr4:118165766
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1539+22082G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165766 | ||||||
| chr4:118165785
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1539+22101G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165785 | ||||||
| chr4:118165860
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1539+22176G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165860 | ||||||
| chr4:118165938
|
T | C | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+22254T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165938 | ||||||
| chr4:118165996
|
A | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1539+22312A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118165996 | ||||||
| chr4:118166024
|
G | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+22340G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166024 | ||||||
| chr4:118166175
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+22491A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166175 | ||||||
| chr4:118166520
|
A | G | 1 | a0001c0010t0003g0171 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1539+22836A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166520 | ||||||
| chr4:118166643
|
A | C | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1539+22959A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166643 | ||||||
| chr4:118166656
|
T | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1539+22972T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166656 | ||||||
| chr4:118166675
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+22991C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166675 | ||||||
| chr4:118166724
|
G | A | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+23040G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166724 | ||||||
| chr4:118166972
|
G | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1539+23288G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118166972 | ||||||
| chr4:118167054
|
GA | G | 7 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+23381delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118167054 | |||||
| chr4:118167118
|
T | C | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+23434T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167118 | ||||||
| chr4:118167193
|
C | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+23509C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167193 | ||||||
| chr4:118167237
|
C | T | 3 | a0001c0003t0002g0188a0001c0003t0002g0189a0001c0003t0002g0190 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1539+23553C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167237 | ||||||
| chr4:118167242
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+23558A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167242 | ||||||
| chr4:118167278
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+23594A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167278 | ||||||
| chr4:118167499
|
A | C | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1539+23815A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167499 | ||||||
| chr4:118167543
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0014g0110 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1539+23859C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167543 | ||||||
| chr4:118167544
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1539+23860G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167544 | ||||||
| chr4:118167598
|
T | G | 67 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(64): Show | 67 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1539+23914T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167598 | ||||||
| chr4:118167812
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1539+24128A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167812 | ||||||
| chr4:118167939
|
C | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0193 | 3 | HG01361.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1539+24255C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118167939 | ||||||
| chr4:118168253
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1539+24569G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168253 | ||||||
| chr4:118168292
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1539+24608C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168292 | ||||||
| chr4:118168345
|
T | A | 4 | a0001c0001t0001g0044a0001c0008t0003g0210a0001c0008t0005g0177others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+24661T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168345 | ||||||
| chr4:118168407
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG01070.hp2 HG01978.hp1 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+24723T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168407 | ||||||
| chr4:118168487
|
A | G | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1539+24803A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168487 | ||||||
| chr4:118168497
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+24813G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168497 | ||||||
| chr4:118168777
|
C | T | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+25093C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168777 | ||||||
| chr4:118168905
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1539+25221A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118168905 | ||||||
| chr4:118169115
|
AT | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+25438delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118169115 | |||||
| chr4:118169144
|
AAAAG | A | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1539+25467_1539+25 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118169144 | |||||
| chr4:118169353
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1539+25669C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169353 | ||||||
| chr4:118169607
|
A | C | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+25923A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169607 | ||||||
| chr4:118169615
|
A | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25931A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169615 | ||||||
| chr4:118169617
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25933A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169617 | ||||||
| chr4:118169618
|
A | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25934A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169618 | ||||||
| chr4:118169619
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25935C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169619 | ||||||
| chr4:118169621
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25937C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169621 | ||||||
| chr4:118169622
|
C | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25938C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169622 | ||||||
| chr4:118169623
|
G | T | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25939G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169623 | ||||||
| chr4:118169625
|
C | A | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+25941C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169625 | ||||||
| chr4:118169658
|
G | A | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+25974G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169658 | ||||||
| chr4:118169716
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1539+26032C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169716 | ||||||
| chr4:118169793
|
C | CA | 41 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1539+26125dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118169793 | |||||
| chr4:118169808
|
A | AG | 5 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+26124_1539+26 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169808 | ||||||
| chr4:118169808
|
A | G | 13 | a0001c0006t0001g0066a0001c0006t0001g0103a0001c0006t0001g0104others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1539+26124A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169808 | ||||||
| chr4:118169861
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+26177A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169861 | ||||||
| chr4:118169934
|
T | C | 18 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1539+26250T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169934 | ||||||
| chr4:118169986
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1539+26302T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118169986 | ||||||
| chr4:118170137
|
T | G | 1 | a0001c0001t0001g0024 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1539+26453T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170137 | ||||||
| chr4:118170229
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1539+26545G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170229 | ||||||
| chr4:118170314
|
A | G | 6 | a0001c0001t0020g0113a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+26630A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170314 | ||||||
| chr4:118170328
|
C | T | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+26644C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170328 | ||||||
| chr4:118170367
|
G | A | 8 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1539+26683G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170367 | ||||||
| chr4:118170367
|
G | T | 43 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(40): Show | 43 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1539+26683G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170367 | ||||||
| chr4:118170438
|
A | G | 24 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1539+26754A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170438 | ||||||
| chr4:118170467
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1539+26783G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170467 | ||||||
| chr4:118170607
|
C | T | 9 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1539+26923C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170607 | ||||||
| chr4:118170665
|
A | G | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1539+26981A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170665 | ||||||
| chr4:118170686
|
A | G | 1 | a0001c0002t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1539+27002A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170686 | ||||||
| chr4:118170744
|
GA | G | 12 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0011g0102others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1539+27066delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118170744 | |||||
| chr4:118170757
|
T | C | 1 | a0001c0004t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1539+27073T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170757 | ||||||
| chr4:118170838
|
T | G | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1539+27154T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170838 | ||||||
| chr4:118170855
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1539+27171T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118170855 | ||||||
| chr4:118171175
|
C | A | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1539+27491C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171175 | ||||||
| chr4:118171180
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1539+27496T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171180 | ||||||
| chr4:118171280
|
G | A | 3 | a0001c0001t0001g0044a0001c0008t0003g0210a0001c0008t0005g0177 | 3 | HG02258.hp2 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+27596G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171280 | ||||||
| chr4:118171289
|
T | A | 1 | a0001c0011t0009g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1539+27605T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171289 | ||||||
| chr4:118171302
|
A | G | 42 | a0001c0001t0001g0044a0001c0001t0001g0184a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1539+27618A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171302 | ||||||
| chr4:118171408
|
G | C | 1 | a0001c0002t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1539+27724G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171408 | ||||||
| chr4:118171455
|
A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 80 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1539+27771A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171455 | ||||||
| chr4:118171523
|
C | CTT | 18 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(15): Show | 18 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1539+27840_1539+27 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118171523 | |||||
| chr4:118171685
|
G | A | 3 | a0001c0001t0001g0044a0001c0008t0003g0210a0001c0008t0005g0177 | 3 | HG02258.hp2 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+28001G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171685 | ||||||
| chr4:118171720
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1539+28036A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171720 | ||||||
| chr4:118171833
|
C | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+28149C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171833 | ||||||
| chr4:118171881
|
C | A | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+28197C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118171881 | ||||||
| chr4:118172037
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1539+28353G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172037 | ||||||
| chr4:118172064
|
T | G | 47 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0002t0001g0029others(44): Show | 47 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1539+28380T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172064 | ||||||
| chr4:118172105
|
T | C | 66 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(63): Show | 66 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1539+28421T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172105 | ||||||
| chr4:118172149
|
A | G | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+28465A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172149 | ||||||
| chr4:118172293
|
A | G | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+28609A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172293 | ||||||
| chr4:118172377
|
G | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+28693G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172377 | ||||||
| chr4:118172431
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1539+28747G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172431 | ||||||
| chr4:118172767
|
T | G | 2 | a0001c0002t0001g0060a0001c0002t0001g0214 | 2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1539+29083T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172767 | ||||||
| chr4:118172768
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+29084G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172768 | ||||||
| chr4:118172823
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1539+29139T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118172823 | ||||||
| chr4:118173134
|
A | ATG | 25 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 25 | HG00639.hp1 HG01243.hp1 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.1539+29470_1539+29 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118173134 | |||||
| chr4:118173134
|
ATG | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 78 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1539+29470_1539+29 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118173134 | |||||
| chr4:118173154
|
G | GTA | 24 | a0001c0002t0001g0060a0001c0002t0001g0064a0001c0002t0001g0072others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1539+29482_1539+29 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118173154 | |||||
| chr4:118173154
|
G | GTGTA | 16 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0061others(13): Show | 16 | HG00597.hp1 HG00738.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.1539+29471_1539+29 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118173154 | |||||
| chr4:118173156
|
A | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+29472A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173156 | ||||||
| chr4:118173188
|
C | A | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1539+29504C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173188 | ||||||
| chr4:118173268
|
A | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+29584A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173268 | ||||||
| chr4:118173310
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.1539+29626C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173310 | ||||||
| chr4:118173331
|
T | C | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1539+29647T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173331 | ||||||
| chr4:118173354
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0142 | 2 | NA18970.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1539+29670C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173354 | ||||||
| chr4:118173722
|
G | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+30038G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118173722 | ||||||
| chr4:118174102
|
AT | A | 31 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0012g0115others(28): Show | 31 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1539+30424delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118174102 | |||||
| chr4:118174110
|
T | G | 1 | a0001c0012t0002g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1539+30426T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118174110 | ||||||
| chr4:118174118
|
C | G | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1539+30434C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118174118 | ||||||
| chr4:118174436
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1539+30752T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118174436 | ||||||
| chr4:118174508
|
GAACT | G | 2 | a0001c0001t0020g0113a0001c0005t0001g0109 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1539+30830_1539+30 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118174508 | |||||
| chr4:118174728
|
A | AT | 5 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | NA18941.hp2 NA18946.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+31050dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118174728 | |||||
| chr4:118174736
|
C | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+31052C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118174736 | ||||||
| chr4:118174893
|
C | T | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+31209C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118174893 | ||||||
| chr4:118175052
|
A | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1539+31368A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175052 | ||||||
| chr4:118175106
|
G | A | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1539+31422G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175106 | ||||||
| chr4:118175429
|
ATAAT | A | 41 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1539+31748_1539+31 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118175429 | |||||
| chr4:118175454
|
G | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+31770G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175454 | ||||||
| chr4:118175507
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1539+31823C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175507 | ||||||
| chr4:118175586
|
T | C | 7 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0133others(4): Show | 7 | HG00597.hp2 HG02027.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+31902T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175586 | ||||||
| chr4:118175587
|
A | AG | 41 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1539+31904dupG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118175587 | |||||
| chr4:118175630
|
G | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+31946G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175630 | ||||||
| chr4:118175681
|
T | C | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1539+31997T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175681 | ||||||
| chr4:118175749
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1539+32065G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175749 | ||||||
| chr4:118175863
|
T | A | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+32179T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175863 | ||||||
| chr4:118175902
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1539+32218G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175902 | ||||||
| chr4:118175968
|
T | C | 47 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0002t0001g0029others(44): Show | 47 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1539+32284T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118175968 | ||||||
| chr4:118176062
|
G | C | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+32378G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176062 | ||||||
| chr4:118176500
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1539+32816A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176500 | ||||||
| chr4:118176531
|
G | A | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1539+32847G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176531 | ||||||
| chr4:118176534
|
A | G | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1539+32850A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176534 | ||||||
| chr4:118176611
|
G | A | 17 | a0001c0001t0012g0115a0001c0004t0003g0194a0001c0004t0003g0196others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1539+32927G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176611 | ||||||
| chr4:118176668
|
A | G | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+32984A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118176668 | ||||||
| chr4:118177043
|
A | G | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1539+33359A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118177043 | ||||||
| chr4:118177073
|
G | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+33389G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118177073 | ||||||
| chr4:118177553
|
A | G | 3 | a0001c0004t0003g0196a0001c0004t0003g0205a0001c0018t0003g0071 | 3 | HG02109.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+33869A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118177553 | ||||||
| chr4:118177638
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1539+33954G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118177638 | ||||||
| chr4:118177677
|
A | G | 47 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0002t0001g0029others(44): Show | 47 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1539+33993A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118177677 | ||||||
| chr4:118178087
|
T | A | 2 | a0001c0001t0020g0113a0001c0005t0001g0109 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1539+34403T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178087 | ||||||
| chr4:118178089
|
A | T | 1 | a0001c0003t0002g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1539+34405A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178089 | ||||||
| chr4:118178154
|
T | A | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+34470T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178154 | ||||||
| chr4:118178333
|
G | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+34649G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178333 | ||||||
| chr4:118178465
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1539+34781G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178465 | ||||||
| chr4:118178491
|
G | A | 17 | a0001c0001t0012g0115a0001c0004t0003g0194a0001c0004t0003g0196others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1539+34807G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178491 | ||||||
| chr4:118178601
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1539+34917C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178601 | ||||||
| chr4:118178918
|
T | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1539+35234T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118178918 | ||||||
| chr4:118179213
|
A | G | 1 | a0001c0004t0001g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1539+35529A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179213 | ||||||
| chr4:118179738
|
C | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+36054C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179738 | ||||||
| chr4:118179772
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+36088T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179772 | ||||||
| chr4:118179792
|
A | G | 1 | a0001c0002t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1539+36108A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179792 | ||||||
| chr4:118179811
|
T | C | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+36127T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179811 | ||||||
| chr4:118179897
|
T | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1539+36213T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118179897 | ||||||
| chr4:118180002
|
C | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+36318C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180002 | ||||||
| chr4:118180138
|
T | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1539+36454T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180138 | ||||||
| chr4:118180151
|
A | G | 41 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1539+36467A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180151 | ||||||
| chr4:118180158
|
G | A | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+36474G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180158 | ||||||
| chr4:118180244
|
T | C | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+36560T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180244 | ||||||
| chr4:118180366
|
T | C | 47 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0002t0001g0029others(44): Show | 47 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1539+36682T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180366 | ||||||
| chr4:118180410
|
T | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+36726T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180410 | ||||||
| chr4:118180500
|
A | C | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1539+36816A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180500 | ||||||
| chr4:118180568
|
T | C | 41 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1539+36884T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180568 | ||||||
| chr4:118180752
|
T | C | 1 | a0001c0002t0001g0172 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1539+37068T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118180752 | ||||||
| chr4:118181219
|
C | A | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+37535C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181219 | ||||||
| chr4:118181250
|
A | G | 7 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(4): Show | 7 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+37566A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181250 | ||||||
| chr4:118181332
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1539+37648G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181332 | ||||||
| chr4:118181657
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1539+37973T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181657 | ||||||
| chr4:118181718
|
C | A | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1539+38034C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181718 | ||||||
| chr4:118181960
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1539+38276G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118181960 | ||||||
| chr4:118182109
|
A | G | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1539+38425A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182109 | ||||||
| chr4:118182383
|
C | T | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+38699C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182383 | ||||||
| chr4:118182529
|
G | A | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1539+38845G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182529 | ||||||
| chr4:118182764
|
A | G | 1 | a0001c0006t0001g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1539+39080A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182764 | ||||||
| chr4:118182851
|
C | T | 33 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1539+39167C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182851 | ||||||
| chr4:118182901
|
G | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+39217G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182901 | ||||||
| chr4:118182902
|
T | G | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+39218T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118182902 | ||||||
| chr4:118182946
|
AAGAC | A | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+39268_1539+39 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118182946 | |||||
| chr4:118183069
|
C | T | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+39385C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183069 | ||||||
| chr4:118183506
|
A | G | 1 | a0001c0011t0009g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1539+39822A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183506 | ||||||
| chr4:118183510
|
T | C | 1 | a0001c0005t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1539+39826T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183510 | ||||||
| chr4:118183631
|
T | C | 1 | a0001c0003t0002g0014 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1539+39947T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183631 | ||||||
| chr4:118183750
|
G | A | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+40066G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183750 | ||||||
| chr4:118183868
|
C | T | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+40184C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183868 | ||||||
| chr4:118183945
|
C | T | 2 | a0001c0001t0020g0113a0001c0005t0001g0109 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1539+40261C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118183945 | ||||||
| chr4:118184076
|
T | C | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1539+40392T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184076 | ||||||
| chr4:118184280
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1540-40211G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184280 | ||||||
| chr4:118184300
|
T | C | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-40191T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184300 | ||||||
| chr4:118184331
|
C | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-40160C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184331 | ||||||
| chr4:118184384
|
C | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1540-40107C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184384 | ||||||
| chr4:118184580
|
C | T | 1 | a0001c0006t0001g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1540-39911C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184580 | ||||||
| chr4:118184585
|
G | GTC | 10 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540-39890_1540-39 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184585 | |||||
| chr4:118184602
|
T | TAC | 26 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0045others(23): Show | 26 | HG00597.hp2 HG01109.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.1540-39849_1540-39 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
T | TACAC | 20 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0140others(17): Show | 20 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1540-39851_1540-39 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
T | TACACAC | 31 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1540-39853_1540-39 others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
T | TACACACA others(1): Show |
23 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0101others(20): Show | 23 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1540-39855_1540-39 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
T | TACACACA others(3): Show |
2 | a0001c0003t0002g0019a0001c0004t0001g0197 | 2 | HG02572.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1540-39857_1540-39 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
T | TACACACA others(5): Show |
2 | a0001c0003t0002g0013a0001c0003t0002g0190 | 2 | HG01175.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1540-39859_1540-39 others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
TAC | T | 19 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0132others(16): Show | 19 | HG01175.hp2 HG01884.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.1540-39849_1540-39 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
TACAC | T | 10 | a0001c0001t0001g0122a0001c0001t0001g0166a0001c0001t0001g0191others(7): Show | 10 | HG01074.hp2 HG01361.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1540-39851_1540-39 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
TACACAC | T | 8 | a0001c0001t0018g0162a0001c0002t0001g0178a0001c0006t0011g0102others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1540-39853_1540-39 others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
TACACACA others(3): Show |
T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1540-39857_1540-39 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184602
|
TACACACA others(5): Show |
T | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1540-39859_1540-39 others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118184602 | |||||
| chr4:118184605
|
A | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-39886A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184605 | ||||||
| chr4:118184606
|
C | T | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-39885C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184606 | ||||||
| chr4:118184644
|
T | C | 4 | a0001c0001t0001g0184a0001c0002t0001g0097a0001c0002t0001g0098others(1): Show | 4 | HG02486.hp1 NA18954.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-39847T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184644 | ||||||
| chr4:118184833
|
G | A | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-39658G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118184833 | ||||||
| chr4:118185115
|
C | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-39376C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185115 | ||||||
| chr4:118185163
|
A | ACATTT | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0015g0049 | 3 | NA18946.hp2 NA18952.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1540-39327_1540-39 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118185163 | |||||
| chr4:118185223
|
T | C | 3 | a0001c0006t0011g0102a0001c0013t0003g0105a0001c0016t0003g0215 | 3 | HG01109.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1540-39268T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185223 | ||||||
| chr4:118185363
|
G | A | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-39128G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185363 | ||||||
| chr4:118185454
|
T | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1540-39037T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185454 | ||||||
| chr4:118185706
|
T | A | 1 | a0001c0003t0002g0012 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1540-38785T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185706 | ||||||
| chr4:118185717
|
C | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-38774C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185717 | ||||||
| chr4:118185880
|
A | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-38611A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185880 | ||||||
| chr4:118185950
|
G | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-38541G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185950 | ||||||
| chr4:118185972
|
T | C | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-38519T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185972 | ||||||
| chr4:118185973
|
C | T | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-38518C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185973 | ||||||
| chr4:118185992
|
T | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-38499T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118185992 | ||||||
| chr4:118186210
|
G | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-38281G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186210 | ||||||
| chr4:118186237
|
A | C | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-38254A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186237 | ||||||
| chr4:118186422
|
G | T | 10 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540-38069G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186422 | ||||||
| chr4:118186488
|
G | C | 4 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(1): Show | 4 | HG00639.hp2 HG01192.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-38003G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186488 | ||||||
| chr4:118186499
|
G | A | 65 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(62): Show | 65 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1540-37992G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186499 | ||||||
| chr4:118186535
|
G | A | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-37956G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186535 | ||||||
| chr4:118186557
|
G | C | 17 | a0001c0001t0012g0115a0001c0004t0003g0194a0001c0004t0003g0196others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-37934G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186557 | ||||||
| chr4:118186873
|
T | G | 8 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0081others(5): Show | 8 | HG00099.hp1 HG00735.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1540-37618T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186873 | ||||||
| chr4:118186922
|
G | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-37569G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186922 | ||||||
| chr4:118186930
|
T | C | 2 | a0001c0005t0004g0108a0001c0017t0001g0207 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1540-37561T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118186930 | ||||||
| chr4:118187038
|
A | G | 17 | a0001c0001t0012g0115a0001c0004t0003g0194a0001c0004t0003g0196others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-37453A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187038 | ||||||
| chr4:118187042
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-37449C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187042 | ||||||
| chr4:118187101
|
A | G | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-37390A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187101 | ||||||
| chr4:118187124
|
T | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-37367T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187124 | ||||||
| chr4:118187203
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1540-37288C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187203 | ||||||
| chr4:118187379
|
A | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-37112A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187379 | ||||||
| chr4:118187476
|
TTC | T | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-37013_1540-37 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118187476 | |||||
| chr4:118187620
|
G | T | 17 | a0001c0001t0012g0115a0001c0004t0003g0194a0001c0004t0003g0196others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-36871G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187620 | ||||||
| chr4:118187722
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1540-36769T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187722 | ||||||
| chr4:118187764
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-36727T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187764 | ||||||
| chr4:118187765
|
T | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-36726T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187765 | ||||||
| chr4:118187835
|
T | C | 48 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0001t0020g0113others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1540-36656T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118187835 | ||||||
| chr4:118188047
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1540-36444T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188047 | ||||||
| chr4:118188281
|
A | G | 1 | a0001c0003t0002g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1540-36210A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188281 | ||||||
| chr4:118188288
|
A | G | 1 | a0001c0003t0007g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1540-36203A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188288 | ||||||
| chr4:118188328
|
T | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-36163T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188328 | ||||||
| chr4:118188360
|
C | T | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-36131C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188360 | ||||||
| chr4:118188365
|
T | C | 39 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1540-36126T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188365 | ||||||
| chr4:118188525
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1540-35966T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188525 | ||||||
| chr4:118188559
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1540-35932A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188559 | ||||||
| chr4:118188700
|
G | A | 1 | a0001c0012t0002g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1540-35791G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188700 | ||||||
| chr4:118188823
|
T | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-35668T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188823 | ||||||
| chr4:118188833
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1540-35658T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118188833 | ||||||
| chr4:118189642
|
T | C | 1 | a0001c0003t0002g0035 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1540-34849T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189642 | ||||||
| chr4:118189698
|
C | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1540-34793C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189698 | ||||||
| chr4:118189851
|
A | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-34640A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189851 | ||||||
| chr4:118189857
|
T | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(3): Show | 6 | HG01074.hp2 HG01975.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-34634T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189857 | ||||||
| chr4:118189857
|
T | G | 31 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(28): Show | 31 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1540-34634T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189857 | ||||||
| chr4:118189974
|
C | T | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1540-34517C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118189974 | ||||||
| chr4:118190020
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG03688.hp1 NA18948.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-34471T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190020 | ||||||
| chr4:118190033
|
T | A | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1540-34458T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190033 | ||||||
| chr4:118190062
|
G | C | 65 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0184others(62): Show | 65 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1540-34429G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190062 | ||||||
| chr4:118190197
|
T | C | 1 | a0001c0001t0001g0003 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1540-34294T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190197 | ||||||
| chr4:118190417
|
T | C | 1 | a0001c0004t0003g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1540-34074T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190417 | ||||||
| chr4:118190642
|
A | G | 1 | a0001c0002t0001g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1540-33849A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190642 | ||||||
| chr4:118190762
|
C | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-33729C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190762 | ||||||
| chr4:118190768
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1540-33723A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190768 | ||||||
| chr4:118190852
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-33639T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190852 | ||||||
| chr4:118190895
|
T | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-33596T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190895 | ||||||
| chr4:118190902
|
A | C | 27 | a0001c0001t0001g0024a0001c0003t0002g0007a0001c0003t0002g0008others(24): Show | 27 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1540-33589A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118190902 | ||||||
| chr4:118191492
|
A | C | 4 | a0001c0007t0001g0200a0001c0007t0001g0201a0001c0007t0001g0203others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-32999A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118191492 | ||||||
| chr4:118191674
|
T | C | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1540-32817T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118191674 | ||||||
| chr4:118191806
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1540-32685T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118191806 | ||||||
| chr4:118191824
|
C | T | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-32667C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118191824 | ||||||
| chr4:118191825
|
G | A | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-32666G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118191825 | ||||||
| chr4:118192253
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1540-32238A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192253 | ||||||
| chr4:118192290
|
T | C | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-32201T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192290 | ||||||
| chr4:118192365
|
A | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1540-32126A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192365 | ||||||
| chr4:118192394
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-32097T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192394 | ||||||
| chr4:118192713
|
GT | G | 29 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(26): Show | 29 | HG00099.hp1 HG00735.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1540-31767delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118192713 | |||||
| chr4:118192724
|
TG | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-31766delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192724 | ||||||
| chr4:118192725
|
G | T | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-31766G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192725 | ||||||
| chr4:118192838
|
G | A | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-31653G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118192838 | ||||||
| chr4:118193262
|
C | T | 24 | a0001c0001t0001g0184a0001c0002t0001g0060a0001c0002t0001g0061others(21): Show | 24 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1540-31229C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193262 | ||||||
| chr4:118193269
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1540-31222C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193269 | ||||||
| chr4:118193311
|
T | C | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1540-31180T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193311 | ||||||
| chr4:118193455
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1540-31036G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193455 | ||||||
| chr4:118193536
|
C | A | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1540-30955C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193536 | ||||||
| chr4:118193593
|
G | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-30898G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193593 | ||||||
| chr4:118193703
|
C | G | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1540-30788C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193703 | ||||||
| chr4:118193767
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1540-30724T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118193767 | ||||||
| chr4:118194079
|
A | G | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1540-30412A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194079 | ||||||
| chr4:118194091
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-30400T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194091 | ||||||
| chr4:118194211
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.1540-30280A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194211 | ||||||
| chr4:118194494
|
G | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-29997G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194494 | ||||||
| chr4:118194589
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-29902G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194589 | ||||||
| chr4:118194604
|
C | T | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-29887C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194604 | ||||||
| chr4:118194698
|
A | C | 48 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0001t0020g0113others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1540-29793A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194698 | ||||||
| chr4:118194725
|
A | G | 48 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0001t0020g0113others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1540-29766A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194725 | ||||||
| chr4:118194727
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1540-29764T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194727 | ||||||
| chr4:118194757
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-29734C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194757 | ||||||
| chr4:118194762
|
C | T | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-29729C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194762 | ||||||
| chr4:118194786
|
C | A | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-29705C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194786 | ||||||
| chr4:118194977
|
T | G | 1 | a0001c0001t0016g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1540-29514T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118194977 | ||||||
| chr4:118195076
|
A | T | 1 | a0001c0002t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1540-29415A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195076 | ||||||
| chr4:118195132
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-29359T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195132 | ||||||
| chr4:118195264
|
A | T | 7 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(4): Show | 7 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-29227A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195264 | ||||||
| chr4:118195670
|
T | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-28821T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195670 | ||||||
| chr4:118195803
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1540-28688C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195803 | ||||||
| chr4:118195934
|
A | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-28557A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118195934 | ||||||
| chr4:118196028
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1540-28463C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118196028 | ||||||
| chr4:118196105
|
T | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1540-28386T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118196105 | ||||||
| chr4:118196378
|
G | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1540-28113G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118196378 | ||||||
| chr4:118196669
|
A | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-27822A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118196669 | ||||||
| chr4:118196731
|
C | A | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1540-27760C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118196731 | ||||||
| chr4:118197050
|
T | C | 19 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1540-27441T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197050 | ||||||
| chr4:118197160
|
CTT | C | 7 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(4): Show | 7 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-27330_1540-27 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197160 | ||||||
| chr4:118197184
|
T | A | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-27307T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197184 | ||||||
| chr4:118197350
|
A | AGATCCAT others(25): Show |
42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-27138_1540-27 others(38): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197350 | |||||
| chr4:118197376
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-27115T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197376 | ||||||
| chr4:118197518
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0004t0001g0197 | 3 | HG01192.hp2 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1540-26973C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197518 | ||||||
| chr4:118197608
|
G | T | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-26883G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197608 | ||||||
| chr4:118197683
|
T | TTCCATGT others(310): Show |
4 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-26797_1540-26 others(323): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197683 | |||||
| chr4:118197683
|
T | TTCCATGT others(311): Show |
1 | a0001c0017t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1540-26797_1540-26 others(324): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197683 | |||||
| chr4:118197683
|
T | TTCCATGT others(313): Show |
1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1540-26797_1540-26 others(326): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197683 | |||||
| chr4:118197803
|
C | CT | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(8): Show | 11 | HG00558.hp2 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-26673dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197803 | |||||
| chr4:118197803
|
C | CTTT | 30 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-26675_1540-26 others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197803 | |||||
| chr4:118197803
|
CTT | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-26674_1540-26 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118197803 | |||||
| chr4:118197855
|
G | A | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-26636G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197855 | ||||||
| chr4:118197991
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1540-26500G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118197991 | ||||||
| chr4:118198058
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1540-26433A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198058 | ||||||
| chr4:118198249
|
T | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002 | 3 | HG01975.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1540-26242T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198249 | ||||||
| chr4:118198383
|
C | A | 11 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(8): Show | 11 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1540-26108C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198383 | ||||||
| chr4:118198710
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1540-25781C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198710 | ||||||
| chr4:118198727
|
TA | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0086others(126): Show | 130 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1540-25754delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118198727 | |||||
| chr4:118198763
|
CT | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-25719delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118198763 | |||||
| chr4:118198773
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00735.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1540-25718G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198773 | ||||||
| chr4:118198857
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-25634T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118198857 | ||||||
| chr4:118199004
|
T | C | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-25487T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118199004 | ||||||
| chr4:118199133
|
T | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-25358T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118199133 | ||||||
| chr4:118199231
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-25260C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118199231 | ||||||
| chr4:118199633
|
G | T | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-24858G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118199633 | ||||||
| chr4:118200013
|
T | A | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-24478T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200013 | ||||||
| chr4:118200129
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1540-24362G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200129 | ||||||
| chr4:118200229
|
T | C | 31 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(28): Show | 31 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1540-24262T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200229 | ||||||
| chr4:118200318
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1540-24173T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200318 | ||||||
| chr4:118200327
|
C | T | 6 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(3): Show | 6 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-24164C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200327 | ||||||
| chr4:118200425
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-24066C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200425 | ||||||
| chr4:118200454
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1540-24037C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200454 | ||||||
| chr4:118200521
|
G | C | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-23970G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200521 | ||||||
| chr4:118200540
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-23951C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200540 | ||||||
| chr4:118200587
|
T | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-23904T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200587 | ||||||
| chr4:118200605
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1540-23886A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200605 | ||||||
| chr4:118200634
|
C | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-23857C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200634 | ||||||
| chr4:118200666
|
T | C | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1540-23825T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200666 | ||||||
| chr4:118200687
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1540-23804G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200687 | ||||||
| chr4:118200773
|
A | G | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-23718A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200773 | ||||||
| chr4:118200891
|
G | A | 1 | a0001c0003t0002g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1540-23600G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118200891 | ||||||
| chr4:118201085
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1540-23406G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201085 | ||||||
| chr4:118201145
|
G | A | 1 | a0001c0016t0003g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1540-23346G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201145 | ||||||
| chr4:118201157
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1540-23334T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201157 | ||||||
| chr4:118201166
|
T | C | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-23325T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201166 | ||||||
| chr4:118201287
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-23204C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201287 | ||||||
| chr4:118201715
|
T | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-22776T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201715 | ||||||
| chr4:118201730
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-22761C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201730 | ||||||
| chr4:118201853
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-22638T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201853 | ||||||
| chr4:118201960
|
G | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1540-22531G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118201960 | ||||||
| chr4:118202026
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-22465C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202026 | ||||||
| chr4:118202087
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1540-22404G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202087 | ||||||
| chr4:118202235
|
G | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-22256G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202235 | ||||||
| chr4:118202254
|
T | C | 1 | a0001c0003t0002g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1540-22237T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202254 | ||||||
| chr4:118202632
|
T | C | 1 | a0001c0002t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1540-21859T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202632 | ||||||
| chr4:118202748
|
A | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-21743A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118202748 | ||||||
| chr4:118203191
|
A | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-21300A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203191 | ||||||
| chr4:118203210
|
T | G | 1 | a0001c0002t0001g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1540-21281T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203210 | ||||||
| chr4:118203327
|
T | C | 7 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(4): Show | 7 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1540-21164T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203327 | ||||||
| chr4:118203342
|
A | G | 1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1540-21149A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203342 | ||||||
| chr4:118203360
|
AT | A | 6 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(3): Show | 6 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-21125delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118203360 | |||||
| chr4:118203363
|
T | G | 6 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(3): Show | 6 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-21128T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203363 | ||||||
| chr4:118203565
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1540-20926T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203565 | ||||||
| chr4:118203899
|
T | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-20592T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203899 | ||||||
| chr4:118203965
|
C | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-20526C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118203965 | ||||||
| chr4:118204217
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1540-20274G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204217 | ||||||
| chr4:118204256
|
TAATTCGG others(4781): Show |
T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-20230_1540-15 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118204256 | |||||
| chr4:118204288
|
TA | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.1540-20189delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118204288 | |||||
| chr4:118204288
|
TAA | T | 28 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0121others(25): Show | 28 | HG00738.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1540-20190_1540-20 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118204288 | |||||
| chr4:118204294
|
A | T | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-20197A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204294 | ||||||
| chr4:118204297
|
A | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1540-20194A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204297 | ||||||
| chr4:118204333
|
A | G | 1 | a0001c0003t0002g0012 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1540-20158A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204333 | ||||||
| chr4:118204570
|
T | C | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1540-19921T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204570 | ||||||
| chr4:118204649
|
A | G | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-19842A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118204649 | ||||||
| chr4:118205180
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-19311T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118205180 | ||||||
| chr4:118205565
|
T | C | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-18926T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118205565 | ||||||
| chr4:118205832
|
CT | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 85 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1540-18641delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118205832 | |||||
| chr4:118205864
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0178 | 2 | NA18970.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1540-18627G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118205864 | ||||||
| chr4:118205990
|
G | A | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1540-18501G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118205990 | ||||||
| chr4:118206236
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1540-18255T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118206236 | ||||||
| chr4:118206243
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1540-18248T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118206243 | ||||||
| chr4:118206659
|
A | C | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-17832A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118206659 | ||||||
| chr4:118206996
|
C | CAT | 4 | a0001c0001t0001g0052a0001c0001t0001g0121a0001c0001t0001g0176others(1): Show | 4 | HG01975.hp1 HG02074.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-17483_1540-17 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118206996 | |||||
| chr4:118207146
|
T | TAC | 8 | a0001c0001t0001g0037a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01433.hp1 HG02055.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1540-17301_1540-17 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TAC | T | 6 | a0001c0001t0008g0183a0001c0002t0001g0069a0001c0002t0001g0070others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-17301_1540-17 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACAC | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0120a0001c0001t0001g0121others(19): Show | 23 | HG00738.hp2 HG01243.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1540-17303_1540-17 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACACAC | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0144a0001c0001t0012g0115others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-17305_1540-17 others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0114a0001c0008t0003g0210a0001c0008t0005g0177others(1): Show | 4 | HG01074.hp2 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-17307_1540-17 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0075others(2): Show | 5 | HG00735.hp1 HG01071.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-17311_1540-17 others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACACACA others(7): Show |
T | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1540-17313_1540-17 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207146
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0044a0001c0003t0002g0008a0001c0003t0002g0009others(3): Show | 6 | HG00639.hp2 HG01192.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-17315_1540-17 others(22): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118207146 | |||||
| chr4:118207201
|
T | G | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-17290T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118207201 | ||||||
| chr4:118207400
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG00558.hp2 NA18942.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-17091G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118207400 | ||||||
| chr4:118207401
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG00558.hp2 NA18942.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-17090C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118207401 | ||||||
| chr4:118207790
|
C | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-16701C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118207790 | ||||||
| chr4:118207892
|
G | C | 14 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1540-16599G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118207892 | ||||||
| chr4:118208182
|
A | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-16309A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208182 | ||||||
| chr4:118208217
|
C | T | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-16274C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208217 | ||||||
| chr4:118208300
|
C | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-16191C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208300 | ||||||
| chr4:118208501
|
A | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-15990A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208501 | ||||||
| chr4:118208514
|
G | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1540-15977G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208514 | ||||||
| chr4:118208529
|
A | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1540-15962A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208529 | ||||||
| chr4:118208570
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1540-15921G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208570 | ||||||
| chr4:118208691
|
T | C | 3 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0174 | 3 | HG00544.hp1 NA18954.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1540-15800T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208691 | ||||||
| chr4:118208770
|
C | A | 1 | a0001c0002t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1540-15721C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118208770 | ||||||
| chr4:118209069
|
G | C | 48 | a0001c0001t0001g0184a0001c0001t0012g0115a0001c0001t0020g0113others(45): Show | 48 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1540-15422G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209069 | ||||||
| chr4:118209108
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0054 | 2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1540-15383T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209108 | ||||||
| chr4:118209281
|
T | C | 4 | a0001c0003t0002g0018a0001c0003t0002g0062a0001c0003t0002g0074others(1): Show | 4 | HG01074.hp1 HG01433.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-15210T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209281 | ||||||
| chr4:118209418
|
T | C | 1 | a0001c0002t0001g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1540-15073T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209418 | ||||||
| chr4:118209432
|
T | G | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-15059T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209432 | ||||||
| chr4:118209516
|
A | G | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-14975A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209516 | ||||||
| chr4:118209581
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1540-14910G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209581 | ||||||
| chr4:118209601
|
G | C | 1 | a0001c0005t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1540-14890G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118209601 | ||||||
| chr4:118210051
|
A | G | 6 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-14440A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210051 | ||||||
| chr4:118210080
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1540-14411A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210080 | ||||||
| chr4:118210138
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-14353T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210138 | ||||||
| chr4:118210179
|
G | A | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-14312G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210179 | ||||||
| chr4:118210198
|
T | C | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1540-14293T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210198 | ||||||
| chr4:118210259
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.1540-14232A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210259 | ||||||
| chr4:118210499
|
C | T | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1540-13992C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210499 | ||||||
| chr4:118210649
|
T | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.1540-13842T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210649 | ||||||
| chr4:118210701
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-13790G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210701 | ||||||
| chr4:118210774
|
C | CA | 12 | a0001c0001t0001g0117a0001c0001t0001g0139a0001c0001t0001g0166others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1540-13698dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118210774 | |||||
| chr4:118210774
|
C | CAA | 7 | a0001c0001t0012g0115a0001c0005t0001g0107a0001c0005t0004g0100others(4): Show | 7 | HG01109.hp2 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-13699_1540-13 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118210774 | |||||
| chr4:118210774
|
CA | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1540-13698delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118210774 | |||||
| chr4:118210789
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1540-13702A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210789 | ||||||
| chr4:118210801
|
G | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-13690G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210801 | ||||||
| chr4:118210974
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1540-13517T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118210974 | ||||||
| chr4:118211209
|
T | C | 1 | a0001c0003t0002g0180 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1540-13282T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211209 | ||||||
| chr4:118211233
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1540-13258A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211233 | ||||||
| chr4:118211256
|
G | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1540-13235G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211256 | ||||||
| chr4:118211302
|
GAAGT | G | 72 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(69): Show | 72 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1540-13185_1540-13 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118211302 | |||||
| chr4:118211311
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1540-13180T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211311 | ||||||
| chr4:118211364
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-13127T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211364 | ||||||
| chr4:118211430
|
A | ATATAAAA others(1): Show |
42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-13059_1540-13 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118211430 | |||||
| chr4:118211790
|
G | A | 2 | a0001c0013t0003g0105a0001c0016t0003g0215 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1540-12701G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211790 | ||||||
| chr4:118211877
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0010g0040others(1): Show | 4 | HG00544.hp2 NA18939.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-12614C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211877 | ||||||
| chr4:118211956
|
C | T | 41 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1540-12535C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211956 | ||||||
| chr4:118211979
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1540-12512T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118211979 | ||||||
| chr4:118212360
|
G | A | 39 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1540-12131G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118212360 | ||||||
| chr4:118212657
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1540-11834C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118212657 | ||||||
| chr4:118212969
|
T | C | 4 | a0001c0003t0002g0008a0001c0003t0002g0009a0001c0003t0002g0010others(1): Show | 4 | HG00639.hp2 HG01192.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-11522T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118212969 | ||||||
| chr4:118213068
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1540-11423T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213068 | ||||||
| chr4:118213153
|
T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1540-11338T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213153 | ||||||
| chr4:118213382
|
C | T | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1540-11109C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213382 | ||||||
| chr4:118213574
|
AAT | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-10903_1540-10 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118213574 | |||||
| chr4:118213600
|
A | G | 1 | a0001c0004t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1540-10891A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213600 | ||||||
| chr4:118213701
|
T | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-10790T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213701 | ||||||
| chr4:118213726
|
A | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-10765A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213726 | ||||||
| chr4:118213806
|
C | CA | 5 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0173others(2): Show | 5 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-10684dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118213806 | |||||
| chr4:118213854
|
T | A | 6 | a0001c0005t0001g0107a0001c0005t0001g0109a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-10637T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213854 | ||||||
| chr4:118213965
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-10526T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213965 | ||||||
| chr4:118213982
|
T | C | 34 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(31): Show | 34 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1540-10509T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118213982 | ||||||
| chr4:118214003
|
T | A | 1 | a0001c0003t0002g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1540-10488T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214003 | ||||||
| chr4:118214016
|
A | G | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1540-10475A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214016 | ||||||
| chr4:118214247
|
G | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-10244G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214247 | ||||||
| chr4:118214445
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1540-10046C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214445 | ||||||
| chr4:118214628
|
T | C | 4 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG01175.hp2 HG01361.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-9863T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214628 | ||||||
| chr4:118214703
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-9788G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214703 | ||||||
| chr4:118214790
|
G | A | 3 | a0001c0006t0011g0102a0001c0013t0003g0105a0001c0016t0003g0215 | 3 | HG01109.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1540-9701G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214790 | ||||||
| chr4:118214883
|
A | T | 1 | a0001c0003t0002g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1540-9608A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214883 | ||||||
| chr4:118214962
|
G | T | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1540-9529G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118214962 | ||||||
| chr4:118215043
|
A | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-9448A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215043 | ||||||
| chr4:118215057
|
C | T | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-9434C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215057 | ||||||
| chr4:118215080
|
T | C | 38 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(35): Show | 38 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1540-9411T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215080 | ||||||
| chr4:118215422
|
A | G | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-9069A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215422 | ||||||
| chr4:118215441
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-9050G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215441 | ||||||
| chr4:118215530
|
T | C | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-8961T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215530 | ||||||
| chr4:118215608
|
C | T | 3 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021 | 3 | HG02148.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1540-8883C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215608 | ||||||
| chr4:118215626
|
CA | C | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1540-8864delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215626 | ||||||
| chr4:118215738
|
C | G | 44 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0184others(41): Show | 44 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1540-8753C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215738 | ||||||
| chr4:118215739
|
A | T | 44 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0184others(41): Show | 44 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1540-8752A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215739 | ||||||
| chr4:118215907
|
T | G | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-8584T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215907 | ||||||
| chr4:118215977
|
A | C | 33 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1540-8514A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118215977 | ||||||
| chr4:118216119
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002 | 3 | HG01975.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1540-8372C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216119 | ||||||
| chr4:118216177
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-8314G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216177 | ||||||
| chr4:118216370
|
T | C | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-8121T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216370 | ||||||
| chr4:118216525
|
T | C | 1 | a0001c0018t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1540-7966T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216525 | ||||||
| chr4:118216527
|
A | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1540-7964A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216527 | ||||||
| chr4:118216664
|
C | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-7827C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216664 | ||||||
| chr4:118216665
|
G | A | 2 | a0001c0001t0001g0167a0001c0003t0002g0152 | 2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1540-7826G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216665 | ||||||
| chr4:118216837
|
A | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002 | 3 | HG01975.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1540-7654A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216837 | ||||||
| chr4:118216850
|
C | T | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1540-7641C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216850 | ||||||
| chr4:118216912
|
T | A | 1 | a0001c0011t0009g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1540-7579T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118216912 | ||||||
| chr4:118217384
|
G | A | 6 | a0001c0006t0011g0102a0001c0009t0003g0065a0001c0009t0021g0067others(3): Show | 6 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-7107G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217384 | ||||||
| chr4:118217482
|
C | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1540-7009C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217482 | ||||||
| chr4:118217572
|
C | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1540-6919C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217572 | ||||||
| chr4:118217705
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1540-6786G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217705 | ||||||
| chr4:118217717
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1540-6774A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217717 | ||||||
| chr4:118217823
|
A | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-6668A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118217823 | ||||||
| chr4:118218131
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG01169.hp2 HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1540-6360C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218131 | ||||||
| chr4:118218292
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1540-6199A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218292 | ||||||
| chr4:118218464
|
C | A | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1540-6027C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218464 | ||||||
| chr4:118218568
|
A | T | 6 | a0001c0005t0001g0107a0001c0005t0001g0109a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-5923A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218568 | ||||||
| chr4:118218738
|
G | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-5753G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218738 | ||||||
| chr4:118218794
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1540-5697C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118218794 | ||||||
| chr4:118219007
|
T | A | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-5484T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219007 | ||||||
| chr4:118219039
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1540-5452G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219039 | ||||||
| chr4:118219272
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1540-5219C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219272 | ||||||
| chr4:118219292
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-5199C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219292 | ||||||
| chr4:118219435
|
T | C | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1540-5056T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219435 | ||||||
| chr4:118219920
|
A | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-4571A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118219920 | ||||||
| chr4:118220043
|
T | A | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1540-4448T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220043 | ||||||
| chr4:118220074
|
T | C | 29 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(26): Show | 29 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1540-4417T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220074 | ||||||
| chr4:118220211
|
G | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-4280G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220211 | ||||||
| chr4:118220371
|
A | G | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1540-4120A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220371 | ||||||
| chr4:118220395
|
T | C | 1 | a0001c0002t0001g0096 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1540-4096T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220395 | ||||||
| chr4:118220537
|
G | A | 1 | a0001c0010t0003g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1540-3954G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220537 | ||||||
| chr4:118220589
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-3902C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220589 | ||||||
| chr4:118220697
|
T | C | 8 | a0001c0004t0019g0195a0001c0006t0011g0102a0001c0009t0003g0065others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1540-3794T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220697 | ||||||
| chr4:118220847
|
T | G | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-3644T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118220847 | ||||||
| chr4:118221199
|
T | A | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-3292T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221199 | ||||||
| chr4:118221226
|
C | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1540-3265C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221226 | ||||||
| chr4:118221226
|
C | T | 6 | a0001c0005t0001g0107a0001c0005t0001g0109a0001c0005t0004g0100others(3): Show | 6 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-3265C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221226 | ||||||
| chr4:118221396
|
G | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1540-3095G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221396 | ||||||
| chr4:118221518
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1540-2973C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221518 | ||||||
| chr4:118221594
|
T | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1540-2897T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221594 | ||||||
| chr4:118221615
|
T | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-2876T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118221615 | ||||||
| chr4:118221992
|
TA | T | 36 | a0001c0001t0001g0057a0001c0001t0001g0120a0001c0001t0001g0124others(33): Show | 36 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1540-2486delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 118221992 | |||||
| chr4:118222184
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0143 | 2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1540-2307T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118222184 | ||||||
| chr4:118222616
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1540-1875G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118222616 | ||||||
| chr4:118222720
|
T | C | 1 | a0001c0002t0001g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1540-1771T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118222720 | ||||||
| chr4:118222919
|
T | C | 2 | a0001c0002t0001g0060a0001c0002t0001g0214 | 2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1540-1572T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118222919 | ||||||
| chr4:118223403
|
T | C | 1 | a0001c0003t0002g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1540-1088T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118223403 | ||||||
| chr4:118223443
|
A | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-1048A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118223443 | ||||||
| chr4:118223628
|
C | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-863C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118223628 | ||||||
| chr4:118224018
|
T | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-473T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118224018 | ||||||
| chr4:118224074
|
G | A | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1540-417G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118224074 | ||||||
| chr4:118224398
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1540-93A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118224398 | ||||||
| chr4:118224449
|
A | G | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-42A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 6/13 | chr4 | 118224449 | ||||||
| chr4:118224803
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1722+130C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118224803 | ||||||
| chr4:118224823
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1722+150G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118224823 | ||||||
| chr4:118224891
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1722+218G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118224891 | ||||||
| chr4:118224999
|
T | C | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1722+326T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118224999 | ||||||
| chr4:118225117
|
C | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1722+444C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225117 | ||||||
| chr4:118225138
|
G | A | 2 | a0001c0003t0002g0026a0001c0003t0006g0023 | 2 | HG02602.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1722+465G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225138 | ||||||
| chr4:118225160
|
T | C | 33 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(30): Show | 33 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1722+487T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225160 | ||||||
| chr4:118225233
|
C | T | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1722+560C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225233 | ||||||
| chr4:118225303
|
A | G | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1722+630A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225303 | ||||||
| chr4:118225504
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1722+831A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225504 | ||||||
| chr4:118225591
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1722+918A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225591 | ||||||
| chr4:118225592
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1722+919T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225592 | ||||||
| chr4:118225593
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1722+920C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225593 | ||||||
| chr4:118225632
|
T | C | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1722+959T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225632 | ||||||
| chr4:118225881
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1723-1005C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225881 | ||||||
| chr4:118225985
|
T | C | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-901T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118225985 | ||||||
| chr4:118226308
|
T | C | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1723-578T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226308 | ||||||
| chr4:118226354
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1723-532T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226354 | ||||||
| chr4:118226393
|
C | T | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1723-493C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226393 | ||||||
| chr4:118226429
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1723-457T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226429 | ||||||
| chr4:118226601
|
T | C | 1 | a0001c0003t0002g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1723-285T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226601 | ||||||
| chr4:118226820
|
A | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1723-66A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226820 | ||||||
| chr4:118226868
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1723-18T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 7/13 | chr4 | 118226868 | ||||||
| chr4:118227126
|
C | T | 41 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1819+144C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227126 | ||||||
| chr4:118227191
|
C | G | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1819+209C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227191 | ||||||
| chr4:118227226
|
TG | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1819+245delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227226 | ||||||
| chr4:118227227
|
G | GT | 41 | a0001c0001t0001g0037a0001c0001t0001g0184a0001c0001t0020g0113others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1819+256dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227227 | |||||
| chr4:118227227
|
G | T | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1819+245G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227227 | ||||||
| chr4:118227238
|
TC | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1819+263delC | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227238 | |||||
| chr4:118227238
|
TCC | T | 8 | a0001c0001t0001g0011a0001c0003t0002g0012a0001c0003t0002g0020others(5): Show | 8 | HG02027.hp1 HG02148.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1819+262_1819+263d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227238 | |||||
| chr4:118227239
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(108): Show | 112 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1819+257C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227239 | ||||||
| chr4:118227240
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1819+258C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227240 | ||||||
| chr4:118227364
|
A | T | 41 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1819+382A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227364 | ||||||
| chr4:118227607
|
C | CT | 37 | a0001c0001t0001g0086a0001c0001t0001g0147a0001c0001t0001g0184others(34): Show | 37 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1819+647dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227607 | |||||
| chr4:118227607
|
CT | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0154a0001c0001t0012g0115others(2): Show | 5 | HG02647.hp2 NA18942.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819+647delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227607 | |||||
| chr4:118227607
|
CTT | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1819+646_1819+647d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227607 | |||||
| chr4:118227607
|
CTTT | C | 32 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(29): Show | 32 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1819+645_1819+647d others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118227607 | |||||
| chr4:118227642
|
C | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1819+660C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227642 | ||||||
| chr4:118227642
|
C | T | 2 | a0001c0002t0001g0064a0001c0002t0001g0077 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1819+660C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227642 | ||||||
| chr4:118227651
|
A | G | 2 | a0001c0002t0001g0064a0001c0002t0001g0077 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1819+669A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227651 | ||||||
| chr4:118227803
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1819+821A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227803 | ||||||
| chr4:118227953
|
A | C | 41 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1819+971A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118227953 | ||||||
| chr4:118228026
|
T | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1819+1044T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118228026 | ||||||
| chr4:118228521
|
T | C | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1819+1539T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118228521 | ||||||
| chr4:118228814
|
A | T | 2 | a0001c0009t0003g0065a0001c0009t0021g0067 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1819+1832A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118228814 | ||||||
| chr4:118228833
|
A | C | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819+1851A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118228833 | ||||||
| chr4:118229112
|
A | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.1819+2130A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229112 | ||||||
| chr4:118229407
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1819+2425C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229407 | ||||||
| chr4:118229439
|
T | C | 1 | a0001c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1819+2457T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229439 | ||||||
| chr4:118229507
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0111others(1): Show | 4 | HG01109.hp1 HG01192.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819+2525G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229507 | ||||||
| chr4:118229566
|
T | C | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1819+2584T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229566 | ||||||
| chr4:118229643
|
T | C | 1 | a0001c0012t0002g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1819+2661T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229643 | ||||||
| chr4:118229865
|
T | C | 4 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0014t0003g0021others(1): Show | 4 | HG02148.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1819+2883T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118229865 | ||||||
| chr4:118230088
|
T | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1820-2924T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230088 | ||||||
| chr4:118230113
|
G | C | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1820-2899G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230113 | ||||||
| chr4:118230202
|
T | C | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1820-2810T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230202 | ||||||
| chr4:118230345
|
G | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1820-2667G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230345 | ||||||
| chr4:118230558
|
G | C | 1 | a0001c0001t0001g0046 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1820-2454G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230558 | ||||||
| chr4:118230622
|
C | A | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1820-2390C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230622 | ||||||
| chr4:118230654
|
A | G | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1820-2358A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118230654 | ||||||
| chr4:118231057
|
G | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1820-1955G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231057 | ||||||
| chr4:118231091
|
T | C | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1820-1921T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231091 | ||||||
| chr4:118231133
|
C | T | 1 | a0001c0003t0002g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1820-1879C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231133 | ||||||
| chr4:118231181
|
C | G | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1820-1831C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231181 | ||||||
| chr4:118231275
|
G | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0165 | 3 | HG01433.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1820-1737G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231275 | ||||||
| chr4:118231343
|
AT | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1820-1668delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231343 | ||||||
| chr4:118231344
|
T | A | 71 | a0001c0001t0001g0166a0001c0001t0001g0184a0001c0001t0012g0115others(68): Show | 71 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1820-1668T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231344 | ||||||
| chr4:118231345
|
A | T | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1820-1667A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231345 | ||||||
| chr4:118231348
|
TA | T | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1820-1661delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118231348 | |||||
| chr4:118231364
|
T | C | 4 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG01175.hp2 HG01361.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820-1648T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231364 | ||||||
| chr4:118231422
|
C | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1820-1590C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231422 | ||||||
| chr4:118231704
|
A | G | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1820-1308A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231704 | ||||||
| chr4:118231754
|
A | G | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1820-1258A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231754 | ||||||
| chr4:118231778
|
C | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1820-1234C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231778 | ||||||
| chr4:118231934
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1820-1078T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231934 | ||||||
| chr4:118231999
|
T | C | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1820-1013T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118231999 | ||||||
| chr4:118232057
|
A | G | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1820-955A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232057 | ||||||
| chr4:118232241
|
T | C | 7 | a0001c0004t0019g0195a0001c0009t0003g0065a0001c0009t0021g0067others(4): Show | 7 | HG01109.hp2 HG02148.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820-771T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232241 | ||||||
| chr4:118232475
|
T | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1820-537T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232475 | ||||||
| chr4:118232476
|
A | T | 42 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(39): Show | 42 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1820-536A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232476 | ||||||
| chr4:118232576
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1820-436T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232576 | ||||||
| chr4:118232683
|
G | GGAAA | 33 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1820-324_1820-321d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118232683 | |||||
| chr4:118232683
|
G | GGAAAGAA others(1): Show |
5 | a0001c0001t0020g0113a0001c0009t0003g0065a0001c0009t0021g0067others(2): Show | 5 | HG02148.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820-328_1820-321d others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 118232683 | |||||
| chr4:118232692
|
C | G | 38 | a0001c0001t0001g0184a0001c0001t0020g0113a0001c0002t0001g0029others(35): Show | 38 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1820-320C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232692 | ||||||
| chr4:118232704
|
G | A | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1820-308G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232704 | ||||||
| chr4:118232813
|
C | T | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1820-199C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232813 | ||||||
| chr4:118232869
|
G | A | 9 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1820-143G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232869 | ||||||
| chr4:118232937
|
C | A | 9 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1820-75C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232937 | ||||||
| chr4:118232966
|
T | C | 1 | a0001c0002t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1820-46T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 8/13 | chr4 | 118232966 | ||||||
| chr4:118233304
|
A | T | 1 | a0001c0003t0002g0180 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1943+169A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233304 | ||||||
| chr4:118233445
|
C | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+310C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233445 | ||||||
| chr4:118233686
|
A | T | 8 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1943+551A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233686 | ||||||
| chr4:118233731
|
T | C | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+596T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233731 | ||||||
| chr4:118233740
|
T | C | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1943+605T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233740 | ||||||
| chr4:118233798
|
G | T | 6 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(3): Show | 6 | HG02148.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1943+663G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233798 | ||||||
| chr4:118233946
|
C | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+811C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233946 | ||||||
| chr4:118233962
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1943+827C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118233962 | ||||||
| chr4:118234074
|
T | C | 29 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(26): Show | 29 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1943+939T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118234074 | ||||||
| chr4:118234243
|
C | A | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1943+1108C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118234243 | ||||||
| chr4:118234707
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1943+1572G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118234707 | ||||||
| chr4:118234722
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1943+1587G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118234722 | ||||||
| chr4:118234835
|
G | A | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1943+1700G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118234835 | ||||||
| chr4:118235045
|
A | AAGGAAGG others(12): Show |
11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1943+1911_1943+191 others(23): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 118235045 | |||||
| chr4:118235048
|
G | GGAAGGAA others(9): Show |
161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1943+1928_1943+192 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 118235048 | |||||
| chr4:118235048
|
G | GGAAGGAA others(13): Show |
3 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0002t0001g0002 | 3 | HG01975.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1943+1931_1943+193 others(24): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 118235048 | |||||
| chr4:118235056
|
G | GGAAGGAA others(9): Show |
30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1943+1928_1943+192 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 118235056 | |||||
| chr4:118235326
|
T | G | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1944-1720T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235326 | ||||||
| chr4:118235378
|
A | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1944-1668A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235378 | ||||||
| chr4:118235429
|
C | A | 1 | a0001c0001t0001g0003 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1944-1617C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235429 | ||||||
| chr4:118235431
|
T | G | 1 | a0001c0002t0001g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1944-1615T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235431 | ||||||
| chr4:118235760
|
T | C | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1944-1286T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235760 | ||||||
| chr4:118235970
|
T | A | 2 | a0001c0001t0020g0113a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1944-1076T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118235970 | ||||||
| chr4:118236393
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1944-653A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118236393 | ||||||
| chr4:118236676
|
T | C | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1944-370T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118236676 | ||||||
| chr4:118236756
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1944-290G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118236756 | ||||||
| chr4:118236843
|
A | C | 33 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(30): Show | 33 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1944-203A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118236843 | ||||||
| chr4:118236951
|
G | A | 1 | a0001c0001t0015g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1944-95G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 9/13 | chr4 | 118236951 | ||||||
| chr4:118237374
|
T | C | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118+154T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237374 | ||||||
| chr4:118237380
|
G | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2118+160G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237380 | ||||||
| chr4:118237464
|
CTAAAT | C | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2118+249_2118+253d others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118237464 | |||||
| chr4:118237486
|
A | T | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2118+266A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237486 | ||||||
| chr4:118237507
|
A | C | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118+287A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237507 | ||||||
| chr4:118237511
|
C | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2118+291C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237511 | ||||||
| chr4:118237611
|
T | C | 2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2118+391T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237611 | ||||||
| chr4:118237631
|
A | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118+411A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237631 | ||||||
| chr4:118237835
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2118+615G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118237835 | ||||||
| chr4:118237892
|
C | CAGG | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118+674_2118+675i others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118237892 | |||||
| chr4:118238121
|
A | AAG | 3 | a0001c0003t0002g0007a0001c0003t0002g0009a0001c0003t0002g0012 | 3 | HG02109.hp1 HG03017.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2118+925_2118+926d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238121 | |||||
| chr4:118238121
|
AAG | A | 6 | a0001c0001t0001g0038a0001c0001t0012g0115a0001c0001t0020g0113others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2118+925_2118+926d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238121 | |||||
| chr4:118238121
|
AAGAG | A | 8 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2118+923_2118+926d others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238121 | |||||
| chr4:118238145
|
GAAAAGAA | G | 21 | a0001c0003t0002g0008a0001c0003t0002g0010a0001c0003t0002g0013others(18): Show | 21 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2118+927_2118+933d others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238145 | |||||
| chr4:118238147
|
A | G | 4 | a0001c0003t0002g0014a0001c0003t0002g0022a0001c0003t0002g0035others(1): Show | 4 | HG00738.hp1 HG01192.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2118+927A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238147 | ||||||
| chr4:118238148
|
AAG | A | 4 | a0001c0003t0002g0014a0001c0003t0002g0022a0001c0003t0002g0035others(1): Show | 4 | HG00738.hp1 HG01192.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2118+930_2118+931d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238148 | |||||
| chr4:118238152
|
A | G | 1 | a0001c0001t0016g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2118+932A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238152 | ||||||
| chr4:118238154
|
GAAAAGAA others(5): Show |
G | 1 | a0001c0008t0003g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2118+935_2118+946d others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238154 | ||||||
| chr4:118238154
|
GAAAAGAA others(9): Show |
G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2118+935_2118+950d others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238154 | ||||||
| chr4:118238155
|
A | AAAAG | 4 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0002t0001g0061others(1): Show | 5 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2118+1003_2118+100 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
A | G | 3 | a0001c0003t0002g0007a0001c0003t0002g0009a0001c0003t0002g0012 | 3 | HG02109.hp1 HG03017.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2118+935A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238155 | ||||||
| chr4:118238155
|
AAAAG | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0056others(13): Show | 16 | HG00597.hp2 HG02451.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.2118+1003_2118+100 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(1): Show |
A | 48 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(45): Show | 48 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.2118+999_2118+1006 others(11): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(5): Show |
A | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(41): Show | 44 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2118+995_2118+1006 others(15): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(9): Show |
A | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0114others(22): Show | 25 | HG01071.hp1 HG01258.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2118+991_2118+1006 others(19): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(13): Show |
A | 11 | a0001c0001t0001g0111a0001c0001t0001g0125a0001c0001t0001g0131others(8): Show | 11 | HG01109.hp1 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118+987_2118+1006 others(23): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(17): Show |
A | 3 | a0001c0001t0001g0167a0001c0002t0001g0064a0001c0005t0004g0100 | 3 | HG00099.hp2 HG02615.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2118+983_2118+1006 others(27): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238155
|
AAAAGAAA others(21): Show |
A | 3 | a0001c0001t0001g0120a0001c0001t0001g0146a0001c0002t0001g0091 | 3 | HG02896.hp1 NA18966.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2118+979_2118+1006 others(31): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238155 | |||||
| chr4:118238158
|
A | G | 4 | a0001c0003t0002g0014a0001c0003t0002g0022a0001c0003t0002g0035others(1): Show | 4 | HG00738.hp1 HG01192.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2118+938A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238158 | ||||||
| chr4:118238162
|
A | AG | 8 | a0001c0003t0002g0013a0001c0003t0002g0016a0001c0003t0002g0019others(5): Show | 8 | HG01243.hp2 HG01975.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.2118+943dupG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238162 | |||||
| chr4:118238163
|
GAAA | G | 5 | a0001c0003t0002g0008a0001c0003t0002g0010a0001c0003t0002g0026others(2): Show | 5 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2118+944_2118+946d others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238163 | ||||||
| chr4:118238163
|
GAAAGAAA | G | 3 | a0001c0003t0002g0025a0001c0003t0002g0034a0001c0003t0002g0190 | 3 | HG01175.hp1 HG02004.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2118+944_2118+950d others(9): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238163 | ||||||
| chr4:118238163
|
GAAAGAAA others(4): Show |
G | 4 | a0001c0003t0002g0018a0001c0003t0002g0062a0001c0003t0002g0188others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118+944_2118+954d others(13): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238163 | ||||||
| chr4:118238163
|
GAAAGAAA others(8): Show |
G | 1 | a0001c0003t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2118+944_2118+958d others(17): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238163 | ||||||
| chr4:118238199
|
GAAAGAAA others(21): Show |
G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2118+981_2118+1008 others(31): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238199 | |||||
| chr4:118238203
|
GAAAGAAA others(17): Show |
G | 3 | a0001c0004t0002g0198a0001c0009t0003g0065a0001c0009t0021g0067 | 3 | HG01884.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2118+985_2118+1008 others(27): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238203 | |||||
| chr4:118238207
|
GAAAGAAA others(13): Show |
G | 2 | a0001c0010t0003g0171a0001c0016t0003g0215 | 2 | HG01109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2118+989_2118+1008 others(23): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238207 | |||||
| chr4:118238215
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2118+995G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238215 | ||||||
| chr4:118238215
|
GAAAGAAA others(5): Show |
G | 2 | a0001c0010t0003g0213a0001c0014t0003g0021 | 2 | HG02148.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2118+997_2118+1008 others(15): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118238215 | |||||
| chr4:118238227
|
A | G | 1 | a0001c0013t0003g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2118+1007A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238227 | ||||||
| chr4:118238276
|
A | G | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2118+1056A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238276 | ||||||
| chr4:118238307
|
A | T | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2118+1087A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238307 | ||||||
| chr4:118238430
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2118+1210T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238430 | ||||||
| chr4:118238448
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2118+1228G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238448 | ||||||
| chr4:118238526
|
G | C | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2118+1306G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238526 | ||||||
| chr4:118238577
|
T | C | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2118+1357T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238577 | ||||||
| chr4:118238607
|
G | C | 1 | a0001c0001t0001g0037 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2118+1387G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238607 | ||||||
| chr4:118238689
|
A | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.2118+1469A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238689 | ||||||
| chr4:118238878
|
G | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-1646G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118238878 | ||||||
| chr4:118239017
|
C | T | 1 | a0001c0003t0002g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2119-1507C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239017 | ||||||
| chr4:118239028
|
A | G | 1 | a0001c0006t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119-1496A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239028 | ||||||
| chr4:118239036
|
G | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-1488G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239036 | ||||||
| chr4:118239153
|
A | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2119-1371A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239153 | ||||||
| chr4:118239188
|
A | G | 6 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(3): Show | 6 | HG02148.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119-1336A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239188 | ||||||
| chr4:118239320
|
T | C | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2119-1204T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239320 | ||||||
| chr4:118239448
|
G | A | 8 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2119-1076G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239448 | ||||||
| chr4:118239497
|
T | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-1027T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239497 | ||||||
| chr4:118239521
|
C | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-1003C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239521 | ||||||
| chr4:118239890
|
C | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-634C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239890 | ||||||
| chr4:118239891
|
C | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-633C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239891 | ||||||
| chr4:118239893
|
G | GAAACACT others(7): Show |
11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-631_2119-630i others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118239893 | ||||||
| chr4:118240186
|
G | C | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2119-338G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240186 | ||||||
| chr4:118240195
|
A | G | 1 | a0001c0003t0002g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2119-329A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240195 | ||||||
| chr4:118240264
|
G | GTAA | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-258_2119-256d others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 118240264 | |||||
| chr4:118240313
|
T | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-211T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240313 | ||||||
| chr4:118240402
|
T | A | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2119-122T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240402 | ||||||
| chr4:118240464
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2119-60A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240464 | ||||||
| chr4:118240485
|
C | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119-39C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 10/13 | chr4 | 118240485 | ||||||
| chr4:118240752
|
C | T | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2289+58C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240752 | ||||||
| chr4:118240754
|
T | C | 1 | a0001c0010t0003g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2289+60T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240754 | ||||||
| chr4:118240789
|
C | G | 6 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(3): Show | 6 | HG02148.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2289+95C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240789 | ||||||
| chr4:118240881
|
A | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2289+187A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240881 | ||||||
| chr4:118240923
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2289+229T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240923 | ||||||
| chr4:118240950
|
A | C | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2289+256A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118240950 | ||||||
| chr4:118241188
|
CTG | C | 3 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00735.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2289+497_2289+498d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 118241188 | |||||
| chr4:118241284
|
C | CCTCGGTT others(1): Show |
11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2289+592_2289+593i others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 118241284 | |||||
| chr4:118241448
|
C | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2290-592C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241448 | ||||||
| chr4:118241512
|
T | TCTC | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2290-526_2290-525i others(5): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 118241512 | |||||
| chr4:118241557
|
A | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2290-483A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241557 | ||||||
| chr4:118241602
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2290-438C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241602 | ||||||
| chr4:118241762
|
TTTTCTAG others(11): Show |
T | 1 | a0001c0001t0001g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2290-277_2290-260d others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241762 | ||||||
| chr4:118241767
|
T | C | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2290-273T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241767 | ||||||
| chr4:118241831
|
C | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2290-209C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241831 | ||||||
| chr4:118241845
|
G | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2290-195G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241845 | ||||||
| chr4:118241861
|
T | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2290-179T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241861 | ||||||
| chr4:118241970
|
A | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2290-70A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 11/13 | chr4 | 118241970 | ||||||
| chr4:118242284
|
G | GA | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+135_2399+136i others(3): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242284 | ||||||
| chr4:118242285
|
G | A | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+136G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242285 | ||||||
| chr4:118242285
|
G | GA | 8 | a0001c0001t0001g0137a0001c0001t0001g0165a0001c0002t0001g0029others(5): Show | 8 | HG01433.hp1 HG02615.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2399+146dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118242285 | |||||
| chr4:118242304
|
C | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+155C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242304 | ||||||
| chr4:118242442
|
A | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+293A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242442 | ||||||
| chr4:118242526
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+377T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242526 | ||||||
| chr4:118242629
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.2399+480T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242629 | ||||||
| chr4:118242638
|
G | A | 2 | a0001c0013t0003g0105a0001c0016t0003g0215 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2399+489G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118242638 | ||||||
| chr4:118243020
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2399+871C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243020 | ||||||
| chr4:118243030
|
G | C | 6 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0007t0001g0200others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399+881G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243030 | ||||||
| chr4:118243089
|
GT | G | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+949delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118243089 | |||||
| chr4:118243118
|
TA | T | 11 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0019g0195others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.2399+978delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118243118 | |||||
| chr4:118243135
|
AG | A | 3 | a0001c0008t0003g0210a0001c0008t0005g0177a0001c0015t0005g0015 | 3 | HG01074.hp2 HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+987delG | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243135 | ||||||
| chr4:118243515
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2399+1366A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243515 | ||||||
| chr4:118243977
|
T | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0193 | 3 | HG01361.hp2 HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2399+1828T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243977 | ||||||
| chr4:118243988
|
G | A | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2399+1839G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118243988 | ||||||
| chr4:118244079
|
C | T | 35 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.2399+1930C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118244079 | ||||||
| chr4:118244098
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2399+1949G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118244098 | ||||||
| chr4:118244180
|
AGTT | A | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+2034_2399+203 others(7): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118244180 | |||||
| chr4:118244256
|
G | A | 8 | a0001c0009t0003g0065a0001c0009t0021g0067a0001c0010t0003g0171others(5): Show | 8 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2399+2107G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118244256 | ||||||
| chr4:118244492
|
T | A | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2399+2343T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118244492 | ||||||
| chr4:118244643
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.2399+2494T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118244643 | ||||||
| chr4:118244717
|
AT | A | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2399+2572delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118244717 | |||||
| chr4:118245229
|
A | G | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2399+3080A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245229 | ||||||
| chr4:118245359
|
TA | T | 2 | a0001c0001t0020g0113a0001c0004t0002g0198 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2399+3212delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118245359 | |||||
| chr4:118245604
|
T | C | 1 | a0001c0001t0012g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2399+3455T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245604 | ||||||
| chr4:118245621
|
A | G | 3 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2399+3472A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245621 | ||||||
| chr4:118245789
|
C | A | 30 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(27): Show | 30 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2399+3640C>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245789 | ||||||
| chr4:118245836
|
T | A | 2 | a0001c0013t0003g0105a0001c0016t0003g0215 | 2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2399+3687T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245836 | ||||||
| chr4:118245947
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2399+3798T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118245947 | ||||||
| chr4:118246008
|
T | A | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2399+3859T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246008 | ||||||
| chr4:118246153
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2399+4004T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246153 | ||||||
| chr4:118246214
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.2399+4065C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246214 | ||||||
| chr4:118246326
|
C | T | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2399+4177C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246326 | ||||||
| chr4:118246355
|
C | T | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2399+4206C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246355 | ||||||
| chr4:118246532
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2399+4383A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246532 | ||||||
| chr4:118246753
|
A | G | 1 | a0001c0006t0011g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2399+4604A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246753 | ||||||
| chr4:118246973
|
A | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2399+4824A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118246973 | ||||||
| chr4:118247034
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2399+4885C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247034 | ||||||
| chr4:118247188
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2399+5039C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247188 | ||||||
| chr4:118247202
|
G | A | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2399+5053G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247202 | ||||||
| chr4:118247206
|
T | TA | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.2399+5072dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118247206 | |||||
| chr4:118247547
|
T | C | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+5398T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247547 | ||||||
| chr4:118247557
|
AAAAG | A | 4 | a0001c0002t0001g0060a0001c0008t0003g0210a0001c0008t0005g0177others(1): Show | 4 | HG01074.hp2 HG02258.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2399+5430_2399+543 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118247557 | |||||
| chr4:118247557
|
AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2399+5418_2399+543 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118247557 | |||||
| chr4:118247673
|
C | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.2399+5524C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247673 | ||||||
| chr4:118247686
|
A | T | 2 | a0001c0008t0003g0210a0001c0008t0005g0177 | 2 | HG02258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2399+5537A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247686 | ||||||
| chr4:118247757
|
T | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.2399+5608T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247757 | ||||||
| chr4:118247782
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2399+5633A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247782 | ||||||
| chr4:118247852
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2400-5647T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118247852 | ||||||
| chr4:118248116
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(47): Show | 51 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2400-5383C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248116 | ||||||
| chr4:118248117
|
G | A | 1 | a0001c0005t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2400-5382G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248117 | ||||||
| chr4:118248219
|
C | G | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2400-5280C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248219 | ||||||
| chr4:118248373
|
ACT | A | 14 | a0001c0001t0020g0113a0001c0004t0002g0198a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2400-5125_2400-512 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248373 | ||||||
| chr4:118248523
|
A | G | 1 | a0001c0003t0002g0180 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2400-4976A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248523 | ||||||
| chr4:118248676
|
G | A | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2400-4823G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248676 | ||||||
| chr4:118248888
|
C | T | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-4611C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248888 | ||||||
| chr4:118248922
|
T | C | 12 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.2400-4577T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118248922 | ||||||
| chr4:118249101
|
C | T | 28 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(25): Show | 28 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.2400-4398C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249101 | ||||||
| chr4:118249126
|
C | T | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2400-4373C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249126 | ||||||
| chr4:118249296
|
T | C | 1 | a0001c0003t0002g0012 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2400-4203T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249296 | ||||||
| chr4:118249600
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.2400-3899G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249600 | ||||||
| chr4:118249731
|
T | TAC | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0101others(17): Show | 20 | HG00597.hp1 HG02647.hp2 HG04184.hp2 others(17): Show |
intron_variant | MODIFIER | c.2400-3738_2400-373 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACAC | 5 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0038others(2): Show | 5 | HG02630.hp2 HG02717.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400-3740_2400-373 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACAC | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(54): Show | 57 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.2400-3742_2400-373 others(10): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0166a0001c0001t0001g0191others(2): Show | 5 | HG01361.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400-3744_2400-373 others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(3): Show |
2 | a0001c0004t0003g0196a0001c0004t0003g0205 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2400-3746_2400-373 others(14): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(5): Show |
3 | a0001c0004t0003g0194a0001c0009t0003g0065a0001c0010t0003g0171 | 3 | HG02451.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2400-3748_2400-373 others(16): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(7): Show |
2 | a0001c0010t0003g0213a0001c0018t0003g0071 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2400-3750_2400-373 others(18): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(9): Show |
1 | a0001c0009t0021g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2400-3752_2400-373 others(20): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
T | TACACACA others(11): Show |
1 | a0001c0014t0003g0021 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2400-3754_2400-373 others(22): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249731
|
TAC | T | 2 | a0001c0003t0002g0074a0001c0004t0002g0198 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2400-3738_2400-373 others(6): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118249731 | |||||
| chr4:118249774
|
T | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2400-3725T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249774 | ||||||
| chr4:118249865
|
C | T | 14 | a0001c0001t0012g0115a0001c0001t0020g0113a0001c0004t0003g0194others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2400-3634C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249865 | ||||||
| chr4:118249873
|
C | G | 35 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.2400-3626C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249873 | ||||||
| chr4:118249967
|
T | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-3532T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249967 | ||||||
| chr4:118249991
|
A | G | 1 | a0001c0004t0019g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2400-3508A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118249991 | ||||||
| chr4:118250003
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.2400-3496C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250003 | ||||||
| chr4:118250061
|
A | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2400-3438A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250061 | ||||||
| chr4:118250343
|
A | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | NA18941.hp1 NA18947.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-3156A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250343 | ||||||
| chr4:118250420
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-3079G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250420 | ||||||
| chr4:118250487
|
C | CT | 16 | a0001c0001t0001g0044a0001c0001t0020g0113a0001c0002t0001g0088others(13): Show | 16 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.2400-2998dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118250487 | |||||
| chr4:118250561
|
C | T | 16 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(13): Show | 16 | HG00597.hp2 HG02027.hp2 NA18612.hp1 others(13): Show |
intron_variant | MODIFIER | c.2400-2938C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250561 | ||||||
| chr4:118250575
|
C | G | 30 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2400-2924C>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250575 | ||||||
| chr4:118250726
|
C | T | 11 | a0001c0001t0001g0121a0001c0001t0001g0166a0001c0001t0001g0176others(8): Show | 11 | HG00639.hp1 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2400-2773C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118250726 | ||||||
| chr4:118251088
|
T | TTTTA | 32 | a0001c0001t0020g0113a0001c0002t0001g0172a0001c0003t0002g0007others(29): Show | 32 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2400-2384_2400-238 others(8): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118251088 | |||||
| chr4:118251088
|
T | TTTTATTT others(1): Show |
9 | a0001c0008t0003g0210a0001c0009t0003g0065a0001c0009t0021g0067others(6): Show | 9 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2400-2388_2400-238 others(12): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118251088 | |||||
| chr4:118251125
|
A | AT | 29 | a0001c0001t0001g0056a0001c0003t0002g0007a0001c0003t0002g0008others(26): Show | 29 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.2400-2370dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118251125 | |||||
| chr4:118251130
|
A | AT | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2400-2355dupT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118251130 | |||||
| chr4:118251130
|
A | T | 32 | a0001c0001t0001g0056a0001c0002t0001g0173a0001c0003t0002g0007others(29): Show | 32 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2400-2369A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251130 | ||||||
| chr4:118251130
|
AT | A | 12 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0019g0195others(9): Show | 12 | HG01109.hp2 HG02148.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2400-2355delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118251130 | |||||
| chr4:118251228
|
G | A | 1 | a0001c0003t0002g0169 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2400-2271G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251228 | ||||||
| chr4:118251260
|
G | A | 4 | a0001c0004t0003g0194a0001c0004t0003g0196a0001c0004t0003g0205others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2400-2239G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251260 | ||||||
| chr4:118251287
|
C | T | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2400-2212C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251287 | ||||||
| chr4:118251306
|
T | C | 35 | a0001c0001t0001g0184a0001c0002t0001g0029a0001c0002t0001g0060others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.2400-2193T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251306 | ||||||
| chr4:118251368
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2400-2131C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251368 | ||||||
| chr4:118251369
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2400-2130G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251369 | ||||||
| chr4:118251615
|
T | G | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-1884T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251615 | ||||||
| chr4:118251736
|
A | C | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2400-1763A>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251736 | ||||||
| chr4:118251799
|
T | C | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2400-1700T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251799 | ||||||
| chr4:118251800
|
A | G | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-1699A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118251800 | ||||||
| chr4:118252052
|
A | T | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2400-1447A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252052 | ||||||
| chr4:118252108
|
G | A | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-1391G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252108 | ||||||
| chr4:118252496
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2400-1003C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252496 | ||||||
| chr4:118252529
|
G | A | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2400-970G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252529 | ||||||
| chr4:118252683
|
G | A | 2 | a0001c0003t0002g0026a0001c0003t0006g0023 | 2 | HG02602.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2400-816G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252683 | ||||||
| chr4:118252772
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2400-727T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252772 | ||||||
| chr4:118252798
|
G | A | 1 | a0001c0004t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2400-701G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252798 | ||||||
| chr4:118252815
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2400-684C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252815 | ||||||
| chr4:118252846
|
G | A | 1 | a0001c0003t0002g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2400-653G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118252846 | ||||||
| chr4:118253103
|
T | C | 1 | a0001c0008t0005g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2400-396T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118253103 | ||||||
| chr4:118253173
|
A | T | 5 | a0001c0005t0001g0107a0001c0005t0004g0100a0001c0005t0004g0106others(2): Show | 5 | HG02615.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2400-326A>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118253173 | ||||||
| chr4:118253175
|
T | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0165 | 3 | HG01433.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2400-324T>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118253175 | ||||||
| chr4:118253408
|
T | A | 31 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(28): Show | 31 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2400-91T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | chr4 | 118253408 | ||||||
| chr4:118253485
|
CT | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(147): Show |
splice_region_variant&intron_variant | LOW | c.2400-3delT | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 118253485 | |||||
| chr4:118253745
|
T | C | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2502+144T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118253745 | ||||||
| chr4:118253942
|
C | T | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2502+341C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118253942 | ||||||
| chr4:118253963
|
G | A | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2502+362G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118253963 | ||||||
| chr4:118254010
|
G | T | 1 | a0001c0004t0003g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2502+409G>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254010 | ||||||
| chr4:118254123
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2502+522T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254123 | ||||||
| chr4:118254245
|
C | CA | 6 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0181others(3): Show | 6 | HG00597.hp2 HG00639.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2502+663dupA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 118254245 | |||||
| chr4:118254245
|
CA | C | 34 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0191others(31): Show | 34 | HG00099.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2502+663delA | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 118254245 | |||||
| chr4:118254245
|
CAA | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.2502+662_2502+663d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 118254245 | |||||
| chr4:118254266
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.2502+665C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254266 | ||||||
| chr4:118254277
|
G | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2502+676G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254277 | ||||||
| chr4:118254426
|
A | G | 1 | a0001c0002t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2502+825A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254426 | ||||||
| chr4:118254519
|
C | T | 31 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(28): Show | 31 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2502+918C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254519 | ||||||
| chr4:118254523
|
A | G | 1 | a0001c0015t0005g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2502+922A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254523 | ||||||
| chr4:118254544
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2502+943C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254544 | ||||||
| chr4:118254578
|
T | C | 1 | a0001c0001t0017g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2502+977T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254578 | ||||||
| chr4:118254664
|
T | A | 2 | a0001c0008t0005g0177a0001c0015t0005g0015 | 2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2503-929T>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254664 | ||||||
| chr4:118254749
|
G | A | 31 | a0001c0003t0002g0007a0001c0003t0002g0008a0001c0003t0002g0009others(28): Show | 31 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2503-844G>A | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254749 | ||||||
| chr4:118254780
|
T | C | 1 | a0001c0003t0002g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2503-813T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118254780 | ||||||
| chr4:118255002
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2503-591T>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118255002 | ||||||
| chr4:118255079
|
C | T | 14 | a0001c0001t0020g0113a0001c0004t0003g0194a0001c0004t0003g0196others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2503-514C>T | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118255079 | ||||||
| chr4:118255306
|
G | C | 1 | a0001c0003t0002g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2503-287G>C | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118255306 | ||||||
| chr4:118255430
|
CTG | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2503-161_2503-160d others(4): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 118255430 | |||||
| chr4:118255548
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2503-45A>G | NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 13/13 | chr4 | 118255548 |