| geneid | 51809 |
|---|---|
| ensemblid | ENSG00000109586.12 |
| hgncid | 4129 |
| symbol | GALNT7 |
| name | polypeptide N-acetylgalactosaminyltransferase 7 |
| refseq_nuc | NM_017423.3 |
| refseq_prot | NP_059119.2 |
| ensembl_nuc | ENST00000265000.9 |
| ensembl_prot | ENSP00000265000.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 173168811 |
| end | 173323967 |
| strand | + |
| ver | v1.2 |
| region | chr4:173168811-173323967 |
| region5000 | chr4:173163811-173328967 |
| regionname0 | GALNT7_chr4_173168811_173323967 |
| regionname5000 | GALNT7_chr4_173163811_173328967 |
| 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 | 657 | 259 | 85 | 55 | 81 | 10 | 26 | 59 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0002 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0003 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0004 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0005 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0007 | 0/0 | 657 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1974 | 144 | 42 | 34 | 47 | 6 | 15 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0002 | 1/1 | 1974 | 84 | 30 | 19 | 21 | 4 | 8 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0003 | 0/0 | 1974 | 17 | 1 | 2 | 12 | 0 | 2 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0004 | 0/0 | 1974 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0005 | 0/0 | 1974 | 5 | 4 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0006 | 0/0 | 1974 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0007 | 0/0 | 1974 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0008 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0009 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0010 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0011 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0012 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| c0013 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| 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 | 2276 | 193 | 57 | 48 | 55 | 9 | 22 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0002 | 0/0 | 2278 | 40 | 13 | 2 | 22 | 0 | 3 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0003 | 0/0 | 2277 | 10 | 7 | 2 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0004 | 0/0 | 2277 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0005 | 0/0 | 2276 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0006 | 0/0 | 2277 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0007 | 0/0 | 2276 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0008 | 0/0 | 2278 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0009 | 0/0 | 2276 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0010 | 0/0 | 2276 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0011 | 0/0 | 2276 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0012 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0013 | 0/0 | 2277 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0014 | 0/0 | 2276 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| t0015 | 0/0 | 2276 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1974 | 144 | 42 | 34 | 47 | 6 | 15 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002 | 1/1 | 1974 | 84 | 30 | 19 | 21 | 4 | 8 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0003 | 0/0 | 1974 | 17 | 1 | 2 | 12 | 0 | 2 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0004 | 0/0 | 1974 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0005 | 0/0 | 1974 | 5 | 4 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0006 | 0/0 | 1974 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0008 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0002c0007 | 0/0 | 1974 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0003c0013 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0004c0011 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0005c0009 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0006c0012 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0007c0010 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4249 | 113 | 30 | 30 | 34 | 5 | 14 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0002 | 0/0 | 4251 | 17 | 5 | 0 | 11 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0003 | 0/0 | 4250 | 4 | 3 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0004 | 0/0 | 4250 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0005 | 0/0 | 4249 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0010 | 0/0 | 4249 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0011 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0014 | 0/0 | 4249 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0001t0015 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0001 | 1/1 | 4249 | 68 | 16 | 18 | 20 | 4 | 8 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0002 | 0/0 | 4251 | 7 | 6 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0003 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0006 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0009 | 0/0 | 4249 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0010 | 0/0 | 4249 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0011 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0002t0013 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0003t0002 | 0/0 | 4251 | 14 | 1 | 2 | 9 | 0 | 2 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0003t0008 | 0/0 | 4251 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0003t0012 | 0/0 | 4251 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0004t0001 | 0/0 | 4249 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0005t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0005t0003 | 0/0 | 4250 | 4 | 3 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0006t0001 | 0/0 | 4249 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0001c0008t0002 | 0/0 | 4251 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0002c0007t0007 | 0/0 | 4249 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0003c0013t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0004c0011t0002 | 0/0 | 4251 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0005c0009t0001 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0006c0012t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| a0007c0010t0003 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | copy fasta | chr4 | 173163811 | 173328967 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0010g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0014g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0010g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0013g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0008t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0002c0007t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0002c0007t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0003c0013t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0004c0011t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0005c0009t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0006c0012t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0007c0010t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | GBR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0129 | EUR | GBR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0249 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00642 | hp2 | a0001 | c0002 | t0010 | g0224 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0181 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0176 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01346 | hp2 | a0007 | c0010 | t0003 | g0097 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0208 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0021 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0085 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02273 | hp2 | a0001 | c0001 | t0014 | g0057 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02523 | hp2 | a0001 | c0008 | t0002 | g0147 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0171 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02630 | hp1 | a0001 | c0005 | t0003 | g0093 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0170 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0098 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0075 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02970 | hp2 | a0006 | c0012 | t0001 | g0193 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0104 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03098 | hp2 | a0003 | c0013 | t0001 | g0175 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03130 | hp1 | a0002 | c0007 | t0007 | g0178 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0099 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03209 | hp1 | a0001 | c0002 | t0009 | g0244 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03453 | hp1 | a0001 | c0002 | t0013 | g0233 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0077 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0172 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0257 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0258 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04184 | hp2 | a0001 | c0005 | t0003 | g0092 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18906 | hp1 | a0002 | c0007 | t0007 | g0177 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18948 | hp2 | a0005 | c0009 | t0001 | g0139 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0251 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0237 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18975 | hp1 | a0001 | c0003 | t0008 | g0254 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19012 | hp1 | a0001 | c0003 | t0012 | g0255 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0245 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19074 | hp2 | a0001 | c0003 | t0008 | g0248 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0225 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0232 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | GIH | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02109 | hp2 | a0001 | c0006 | t0001 | g0074 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0084 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03471 | hp1 | a0001 | c0005 | t0003 | g0095 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG06807 | hp2 | a0004 | c0011 | t0002 | g0180 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0230 | REF | REF | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0197 | REF | REF | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173168938
|
C | T | 1 | a0007 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.103C>T | p.Pro35Ser | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/12 | 128/4249 | 103/1974 | 35/657 | chr4 | 173168938 | ||
| chr4:173248208
|
A | G | 1 | a0003 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.355A>G | p.Thr119Ala | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/12 | 380/4249 | 355/1974 | 119/657 | chr4 | 173248208 | ||
| chr4:173248242
|
G | A | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.389G>A | p.Gly130Glu | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/12 | 414/4249 | 389/1974 | 130/657 | chr4 | 173248242 | ||
| chr4:173295400
|
C | G | 1 | a0002 | 2 | HG03130.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.759C>G | p.His253Gln | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 4/12 | 784/4249 | 759/1974 | 253/657 | chr4 | 173295400 | ||
| chr4:173295837
|
A | T | 1 | a0006 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.959A>T | p.Lys320Met | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/12 | 984/4249 | 959/1974 | 320/657 | chr4 | 173295837 | ||
| chr4:173303996
|
A | T | 1 | a0005 | 1 | NA18948.hp2 | missense_variant&splice_region_variant | MODERATE | c.1267A>T | p.Ile423Leu | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/12 | 1292/4249 | 1267/1974 | 423/657 | chr4 | 173303996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173168853
|
G | A | 7 | a0001c0001a0001c0004a0001c0005others(4): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
synonymous_variant | LOW | c.18G>A | p.Gly6Gly | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/12 | 43/4249 | 18/1974 | 6/657 | chr4 | 173168853 | ||
| chr4:173298139
|
A | T | 3 | a0001c0005a0004c0011a0007c0010 | 7 | HG01346.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.990A>T | p.Ile330Ile | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/12 | 1015/4249 | 990/1974 | 330/657 | chr4 | 173298139 | ||
| chr4:173302131
|
T | C | 1 | a0001c0004 | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1233T>C | p.Ile411Ile | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/12 | 1258/4249 | 1233/1974 | 411/657 | chr4 | 173302131 | ||
| chr4:173314029
|
G | T | 1 | a0001c0006 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.1461G>T | p.Ser487Ser | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/12 | 1486/4249 | 1461/1974 | 487/657 | chr4 | 173314029 | ||
| chr4:173318553
|
C | T | 2 | a0001c0003a0001c0008 | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
synonymous_variant | LOW | c.1830C>T | p.Tyr610Tyr | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/12 | 1855/4249 | 1830/1974 | 610/657 | chr4 | 173318553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173321836
|
C | T | 2 | a0001c0001t0011a0001c0002t0011 | 2 | HG01884.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*119C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 119 | chr4 | 173321836 | |||||
| chr4:173321871
|
A | AT | 5 | a0001c0001t0003a0001c0002t0003a0001c0002t0006others(2): Show | 13 | HG01081.hp2 HG01346.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*158dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 159 | INFO_REALIGN_3_PRIME | chr4 | 173321871 | ||||
| chr4:173321897
|
G | T | 2 | a0001c0001t0010a0001c0002t0010 | 2 | HG00140.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*180G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 180 | chr4 | 173321897 | |||||
| chr4:173321987
|
T | G | 1 | a0002c0007t0007 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 270 | chr4 | 173321987 | |||||
| chr4:173322115
|
A | C | 1 | a0001c0001t0015 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 398 | chr4 | 173322115 | |||||
| chr4:173322479
|
C | G | 5 | a0001c0001t0005a0001c0001t0011a0001c0002t0009others(2): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*762C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 762 | chr4 | 173322479 | |||||
| chr4:173322480
|
T | C | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0013others(5): Show | 44 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*763T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 763 | chr4 | 173322480 | |||||
| chr4:173322796
|
G | A | 2 | a0001c0003t0008a0001c0003t0012 | 3 | NA18975.hp1 NA19012.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1079G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1079 | chr4 | 173322796 | |||||
| chr4:173322881
|
T | C | 1 | a0001c0003t0012 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1164 | chr4 | 173322881 | |||||
| chr4:173323065
|
G | A | 1 | a0001c0002t0009 | 2 | HG03209.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1348 | chr4 | 173323065 | |||||
| chr4:173323084
|
A | AT | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0013others(5): Show | 44 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1368dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1369 | INFO_REALIGN_3_PRIME | chr4 | 173323084 | ||||
| chr4:173323127
|
T | TA | 8 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(5): Show | 46 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1423dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1424 | INFO_REALIGN_3_PRIME | chr4 | 173323127 | ||||
| chr4:173323224
|
T | C | 1 | a0001c0002t0006 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1507 | chr4 | 173323224 | |||||
| chr4:173323362
|
T | C | 5 | a0001c0001t0005a0001c0001t0011a0001c0002t0009others(2): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1645T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1645 | chr4 | 173323362 | |||||
| chr4:173323485
|
T | C | 1 | a0002c0007t0007 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1768T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1768 | chr4 | 173323485 | |||||
| chr4:173323953
|
T | G | 1 | a0001c0001t0014 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2236T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 2236 | chr4 | 173323953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173169044
|
C | CG | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+87dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173169044 | |||||
| chr4:173169138
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+177C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169138 | ||||||
| chr4:173169224
|
G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+263G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169224 | ||||||
| chr4:173169230
|
G | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.126+269G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169230 | ||||||
| chr4:173169267
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+306G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169267 | ||||||
| chr4:173169336
|
C | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.126+375C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169336 | ||||||
| chr4:173169417
|
A | C | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.126+456A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169417 | ||||||
| chr4:173169427
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.126+466C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169427 | ||||||
| chr4:173169528
|
G | A | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+567G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169528 | ||||||
| chr4:173169645
|
G | C | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+684G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169645 | ||||||
| chr4:173169704
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+743C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169704 | ||||||
| chr4:173169731
|
G | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+770G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169731 | ||||||
| chr4:173169781
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+820C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169781 | ||||||
| chr4:173169855
|
G | T | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+894G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169855 | ||||||
| chr4:173169928
|
C | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+967C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169928 | ||||||
| chr4:173169969
|
G | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.126+1008G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169969 | ||||||
| chr4:173169975
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.126+1014G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169975 | ||||||
| chr4:173170065
|
G | A | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+1104G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170065 | ||||||
| chr4:173170133
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.126+1172C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170133 | ||||||
| chr4:173170156
|
A | G | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1195A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170156 | ||||||
| chr4:173170360
|
A | G | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+1399A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170360 | ||||||
| chr4:173170366
|
A | G | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126+1405A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170366 | ||||||
| chr4:173170843
|
G | A | 17 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(14): Show | 17 | HG00423.hp1 HG01192.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+1882G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170843 | ||||||
| chr4:173171061
|
AATTAAC | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | NA18946.hp1 NA18979.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+2106_126+2111d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173171061 | |||||
| chr4:173171179
|
A | C | 7 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(4): Show | 7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+2218A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171179 | ||||||
| chr4:173171406
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.126+2445T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171406 | ||||||
| chr4:173171437
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2476G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171437 | ||||||
| chr4:173171492
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.126+2531G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171492 | ||||||
| chr4:173171542
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(5): Show | 8 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171542 | ||||||
| chr4:173171640
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2679A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171640 | ||||||
| chr4:173171662
|
C | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+2701C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171662 | ||||||
| chr4:173171851
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2890G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171851 | ||||||
| chr4:173172032
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+3071G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172032 | ||||||
| chr4:173172081
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+3120G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172081 | ||||||
| chr4:173172238
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+3277C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172238 | ||||||
| chr4:173172381
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+3420C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172381 | ||||||
| chr4:173172437
|
A | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+3476A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172437 | ||||||
| chr4:173172556
|
CA | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(37): Show | 40 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.126+3597delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173172556 | |||||
| chr4:173172793
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+3832T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172793 | ||||||
| chr4:173172841
|
A | G | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+3880A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172841 | ||||||
| chr4:173172892
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(21): Show | 24 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+3931C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172892 | ||||||
| chr4:173173045
|
T | G | 24 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(21): Show | 24 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+4084T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173045 | ||||||
| chr4:173173090
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+4129G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173090 | ||||||
| chr4:173173131
|
A | G | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+4170A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173131 | ||||||
| chr4:173173380
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(102): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.126+4419T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173380 | ||||||
| chr4:173173439
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+4478A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173439 | ||||||
| chr4:173173516
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+4555A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173516 | ||||||
| chr4:173173600
|
A | C | 1 | a0001c0005t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126+4639A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173600 | ||||||
| chr4:173173623
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0002g0040others(1): Show | 4 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4662C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173623 | ||||||
| chr4:173173683
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.126+4722C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173683 | ||||||
| chr4:173173738
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.126+4777T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173738 | ||||||
| chr4:173173789
|
G | A | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+4828G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173789 | ||||||
| chr4:173173791
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+4830T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173791 | ||||||
| chr4:173173952
|
A | G | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+4991A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173952 | ||||||
| chr4:173174618
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+5657A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174618 | ||||||
| chr4:173174761
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 54 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+5800C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174761 | ||||||
| chr4:173174918
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5957G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174918 | ||||||
| chr4:173175038
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+6077G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175038 | ||||||
| chr4:173175116
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+6155G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175116 | ||||||
| chr4:173175486
|
C | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+6525C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175486 | ||||||
| chr4:173175527
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+6566C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175527 | ||||||
| chr4:173175549
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+6588C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175549 | ||||||
| chr4:173175623
|
A | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+6662A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175623 | ||||||
| chr4:173175945
|
C | T | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+6984C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175945 | ||||||
| chr4:173175989
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(14): Show | 17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+7028C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175989 | ||||||
| chr4:173176030
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+7069G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176030 | ||||||
| chr4:173176056
|
A | G | 9 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+7095A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176056 | ||||||
| chr4:173176072
|
CA | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+7123delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173176072 | |||||
| chr4:173176188
|
A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+7227A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176188 | ||||||
| chr4:173176193
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7232A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176193 | ||||||
| chr4:173176285
|
G | C | 3 | a0001c0004t0001g0076a0001c0004t0001g0077a0001c0004t0001g0084 | 3 | HG02486.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+7324G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176285 | ||||||
| chr4:173176476
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+7515T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176476 | ||||||
| chr4:173176496
|
T | C | 1 | a0001c0003t0002g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.126+7535T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176496 | ||||||
| chr4:173176577
|
G | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+7616G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176577 | ||||||
| chr4:173176863
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.126+7902G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176863 | ||||||
| chr4:173176866
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+7905T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176866 | ||||||
| chr4:173176909
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+7948G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176909 | ||||||
| chr4:173176975
|
C | G | 2 | a0001c0004t0001g0076a0001c0004t0001g0077 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+8014C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176975 | ||||||
| chr4:173177075
|
A | C | 51 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+8114A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177075 | ||||||
| chr4:173177124
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+8163T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177124 | ||||||
| chr4:173177349
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+8388T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177349 | ||||||
| chr4:173177633
|
A | C | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+8672A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177633 | ||||||
| chr4:173177681
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+8720T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177681 | ||||||
| chr4:173177998
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+9037T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177998 | ||||||
| chr4:173178004
|
AGTCTGTG others(122): Show |
A | 5 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(2): Show | 5 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9045_126+9173d others(2): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178004 | |||||
| chr4:173178007
|
CTG | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0054others(15): Show | 18 | HG00323.hp2 HG00621.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+9091_126+9092d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178007
|
CTGTG | C | 41 | a0001c0001t0001g0051a0001c0001t0001g0108a0001c0001t0001g0163others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+9089_126+9092d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178007
|
CTGTGTG | C | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+9087_126+9092d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178007
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG00639.hp1 HG01257.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+9085_126+9092d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178007
|
CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0162a0001c0002t0001g0202a0001c0002t0002g0182 | 3 | HG01081.hp1 HG02135.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.126+9083_126+9092d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178007
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0002t0001g0201 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.126+9079_126+9092d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | |||||
| chr4:173178044
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.126+9083T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178044 | ||||||
| chr4:173178044
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+9085_126+9094d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178044 | |||||
| chr4:173178046
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0107others(10): Show | 13 | HG00323.hp2 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+9085T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178046 | ||||||
| chr4:173178046
|
T | TGC | 8 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 8 | HG00423.hp2 HG00597.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9086_126+9087i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178046 | |||||
| chr4:173178046
|
TGTGTGTG others(9): Show |
T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(2): Show | 5 | HG01257.hp1 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9087_126+9102d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178046 | |||||
| chr4:173178047
|
GTGTGTGC others(5): Show |
G | 2 | a0001c0001t0002g0040a0001c0003t0002g0169 | 2 | HG02040.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.126+9087_126+9098d others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178047 | ||||||
| chr4:173178048
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0044others(24): Show | 27 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+9087T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178048 | ||||||
| chr4:173178048
|
T | TGC | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG00280.hp1 HG01361.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | |||||
| chr4:173178048
|
T | TGCGC | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(7): Show | 10 | HG00741.hp2 HG01884.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | |||||
| chr4:173178048
|
T | TGCGCGC | 5 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(2): Show | 5 | HG00140.hp2 HG02056.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | |||||
| chr4:173178048
|
TGTGTGCG others(7): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126+9089_126+9102d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | |||||
| chr4:173178049
|
GTGTGCGC others(3): Show |
G | 7 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0002g0022others(4): Show | 7 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+9089_126+9098d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178049 | ||||||
| chr4:173178050
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.126+9089T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178050 | ||||||
| chr4:173178050
|
T | TGCGC | 5 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG00741.hp1 HG01943.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9090_126+9091i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | |||||
| chr4:173178050
|
T | TGCGCGC | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0134others(7): Show | 10 | HG00558.hp2 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+9090_126+9091i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | |||||
| chr4:173178050
|
T | TGCGCGCG others(3): Show |
1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.126+9090_126+9091i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | |||||
| chr4:173178050
|
T | TGCGTGCG others(1): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0004t0001g0104 | 3 | HG01346.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.126+9090_126+9091i others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | |||||
| chr4:173178050
|
TGTGCGC | T | 4 | a0001c0001t0001g0266a0001c0001t0002g0029a0001c0004t0001g0006others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9091_126+9096d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | |||||
| chr4:173178051
|
GTGCGCGC others(1): Show |
G | 5 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG02602.hp1 NA18906.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9091_126+9098d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178051 | ||||||
| chr4:173178052
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.126+9091T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178052 | ||||||
| chr4:173178052
|
T | TGCGCGC | 3 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG02572.hp1 HG02738.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126+9092_126+9097d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGCGCGCG others(1): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0158others(3): Show | 6 | HG01934.hp2 NA18946.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9097_126+9098i others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGCGCGCG others(3): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG03927.hp2 NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.126+9097_126+9098i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGCGCGCG others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+9097_126+9098i others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGCGTGCG others(3): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0265 | 2 | NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.126+9094_126+9095i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGCGCG others(3): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0008t0002g0147 | 3 | HG02080.hp2 HG02523.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGCG others(5): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG01074.hp1 HG03017.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.126+9092_126+9093i others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGCG others(9): Show |
1 | a0001c0001t0001g0152 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGTG others(3): Show |
1 | a0001c0002t0001g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0161 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178052
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | |||||
| chr4:173178053
|
GCGCGCA | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0079a0001c0001t0002g0031others(3): Show | 6 | HG01081.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+9098_126+9103d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178053 | |||||
| chr4:173178054
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(19): Show | 22 | HG01891.hp1 HG01993.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+9093C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178054 | ||||||
| chr4:173178055
|
GCGCA | G | 11 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0002g0033others(8): Show | 11 | HG01891.hp1 HG02257.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+9098_126+9101d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178055 | |||||
| chr4:173178056
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0082others(13): Show | 16 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+9095C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178056 | ||||||
| chr4:173178057
|
GCA | G | 5 | a0001c0001t0001g0082a0001c0001t0002g0038a0001c0001t0003g0083others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9098_126+9099d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178057 | |||||
| chr4:173178058
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0005g0086others(2): Show | 5 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9097C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178058 | ||||||
| chr4:173178058
|
CACGCGCG others(1): Show |
C | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+9098_126+9105d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178058 | ||||||
| chr4:173178059
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0045others(47): Show | 50 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+9098A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178059 | ||||||
| chr4:173178060
|
C | T | 8 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9099C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178060 | ||||||
| chr4:173178062
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(3): Show | 6 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9101C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178062 | ||||||
| chr4:173178066
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.126+9105T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178066 | ||||||
| chr4:173178069
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+9108G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178069 | ||||||
| chr4:173178071
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.126+9110A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178071 | ||||||
| chr4:173178081
|
A | G | 1 | a0004c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+9120A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178081 | ||||||
| chr4:173178141
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+9180A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178141 | ||||||
| chr4:173178306
|
A | G | 14 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+9345A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178306 | ||||||
| chr4:173178471
|
G | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+9510G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178471 | ||||||
| chr4:173178505
|
T | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+9544T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178505 | ||||||
| chr4:173178800
|
T | A | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+9839T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178800 | ||||||
| chr4:173178829
|
G | C | 2 | a0001c0001t0001g0096a0001c0005t0003g0092 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.126+9868G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178829 | ||||||
| chr4:173178919
|
A | T | 3 | a0001c0004t0001g0006a0001c0005t0003g0093a0001c0005t0003g0095 | 3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.126+9958A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178919 | ||||||
| chr4:173179386
|
T | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(5): Show | 8 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+10425T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179386 | ||||||
| chr4:173179392
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.126+10431T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179392 | ||||||
| chr4:173179542
|
G | T | 1 | a0001c0001t0004g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+10581G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179542 | ||||||
| chr4:173179789
|
GAAAACAA others(3): Show |
G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.126+10838_126+1084 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173179789 | |||||
| chr4:173179899
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+10938C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179899 | ||||||
| chr4:173179970
|
C | T | 1 | a0001c0001t0005g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+11009C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179970 | ||||||
| chr4:173179971
|
G | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+11010G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179971 | ||||||
| chr4:173180004
|
T | C | 1 | a0001c0001t0005g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+11043T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180004 | ||||||
| chr4:173180081
|
T | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+11120T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180081 | ||||||
| chr4:173180294
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+11333A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180294 | ||||||
| chr4:173180326
|
C | CT | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.126+11383dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173180326 | |||||
| chr4:173180326
|
C | CTT | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 69 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.126+11382_126+1138 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173180326 | |||||
| chr4:173180378
|
A | G | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+11417A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180378 | ||||||
| chr4:173180547
|
C | T | 1 | a0001c0006t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.126+11586C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180547 | ||||||
| chr4:173180804
|
A | G | 3 | a0001c0002t0001g0253a0001c0003t0002g0252a0001c0003t0002g0256 | 3 | NA18946.hp2 NA18971.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.126+11843A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180804 | ||||||
| chr4:173180951
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.126+11990T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180951 | ||||||
| chr4:173181118
|
C | T | 3 | a0001c0004t0001g0076a0001c0004t0001g0077a0001c0004t0001g0084 | 3 | HG02486.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+12157C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181118 | ||||||
| chr4:173181246
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.126+12285G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181246 | ||||||
| chr4:173181285
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+12324G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181285 | ||||||
| chr4:173181317
|
A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+12356A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181317 | ||||||
| chr4:173181326
|
T | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+12365T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181326 | ||||||
| chr4:173181539
|
A | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+12578A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181539 | ||||||
| chr4:173181603
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+12642T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181603 | ||||||
| chr4:173182200
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.126+13239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182200 | ||||||
| chr4:173182334
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.126+13373T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182334 | ||||||
| chr4:173182396
|
T | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.126+13435T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182396 | ||||||
| chr4:173182444
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+13483G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182444 | ||||||
| chr4:173182486
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 7 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+13525C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182486 | ||||||
| chr4:173182604
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+13643C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182604 | ||||||
| chr4:173182637
|
A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+13676A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182637 | ||||||
| chr4:173182649
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+13688G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182649 | ||||||
| chr4:173182661
|
T | TAC | 30 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0069others(27): Show | 30 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13734_126+1373 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACAC | 17 | a0001c0001t0001g0149a0001c0002t0001g0014a0001c0002t0001g0019others(14): Show | 17 | HG00621.hp2 HG00639.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+13732_126+1373 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACACAC | 3 | a0001c0001t0002g0028a0001c0002t0001g0183a0003c0013t0001g0175 | 3 | HG02602.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.126+13730_126+1373 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 9 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+13728_126+1373 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACACACA others(3): Show |
7 | a0001c0001t0002g0025a0001c0001t0002g0033a0001c0001t0002g0034others(4): Show | 7 | HG02723.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+13726_126+1373 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACACACA others(5): Show |
5 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+13724_126+1373 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.126+13720_126+1373 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
TAC | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0094others(10): Show | 13 | HG01346.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+13734_126+1373 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
TACAC | T | 8 | a0001c0001t0001g0153a0001c0001t0005g0072a0001c0001t0005g0085others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+13732_126+1373 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182661
|
TACACAC | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(14): Show | 17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+13730_126+1373 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | |||||
| chr4:173182699
|
G | A | 1 | a0001c0002t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.126+13738G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182699 | ||||||
| chr4:173182738
|
T | TAC | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(42): Show | 45 | HG00323.hp2 HG01071.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.126+13803_126+1380 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | |||||
| chr4:173182738
|
T | TACAC | 16 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+13801_126+1380 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | |||||
| chr4:173182738
|
T | TACACACA others(1): Show |
15 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0003t0002g0021others(12): Show | 15 | HG00423.hp1 HG02135.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+13797_126+1380 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | |||||
| chr4:173182738
|
TAC | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(28): Show | 31 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+13803_126+1380 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | |||||
| chr4:173182738
|
TACAC | T | 6 | a0001c0002t0001g0227a0001c0002t0002g0020a0001c0002t0002g0240others(3): Show | 6 | HG00323.hp1 HG02809.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+13801_126+1380 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | |||||
| chr4:173182752
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.126+13791C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182752 | ||||||
| chr4:173182817
|
T | TAC | 109 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(106): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+13882_126+1388 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACAC | 8 | a0001c0001t0001g0002a0001c0001t0001g0107a0001c0001t0001g0114others(5): Show | 8 | HG01891.hp1 HG02602.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+13880_126+1388 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACACACA others(3): Show |
1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+13874_126+1388 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACACACA others(5): Show |
3 | a0001c0002t0009g0244a0001c0002t0009g0245a0004c0011t0002g0180 | 3 | HG03209.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.126+13872_126+1388 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACACACA others(7): Show |
1 | a0001c0002t0002g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126+13870_126+1388 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACACACA others(9): Show |
3 | a0001c0002t0002g0020a0001c0002t0002g0241a0001c0002t0002g0242 | 3 | HG02809.hp2 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.126+13868_126+1388 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
T | TACACACA others(13): Show |
1 | a0001c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+13864_126+1388 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
TACAC | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+13880_126+1388 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182817
|
TACACAC | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+13878_126+1388 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | |||||
| chr4:173182873
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+13912A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182873 | ||||||
| chr4:173182925
|
T | TAC | 6 | a0001c0002t0001g0014a0001c0002t0001g0185a0001c0002t0001g0203others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+13985_126+1398 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182925
|
T | TACAC | 8 | a0001c0001t0001g0266a0001c0002t0002g0020a0001c0002t0002g0240others(5): Show | 8 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+13983_126+1398 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182925
|
T | TACACACA others(1): Show |
15 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(12): Show | 15 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+13979_126+1398 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182925
|
T | TACACACA others(3): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0048others(27): Show | 30 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13977_126+1398 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182925
|
T | TACACACA others(5): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0030others(33): Show | 36 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+13975_126+1398 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182925
|
T | TACACACA others(7): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0094others(10): Show | 13 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+13973_126+1398 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | |||||
| chr4:173182941
|
C | CACACAG | 5 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+13985_126+1398 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182941 | |||||
| chr4:173183043
|
A | AAC | 18 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0069others(15): Show | 18 | HG00140.hp2 HG01255.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+14129_126+1413 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
A | AACAC | 6 | a0001c0002t0001g0018a0001c0002t0001g0183a0001c0002t0001g0194others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14127_126+1413 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
A | AACACACA others(5): Show |
1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+14119_126+1413 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
A | AACACACA others(8): Show |
1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+14094_126+1409 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AAC | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(49): Show | 52 | HG00323.hp2 HG00558.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.126+14129_126+1413 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACAC | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(19): Show | 22 | HG00621.hp2 HG00741.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.126+14127_126+1413 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACAC | A | 15 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0066others(12): Show | 15 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+14125_126+1413 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(1): Show |
A | 44 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0047others(41): Show | 44 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+14123_126+1413 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0055a0001c0001t0001g0096a0001c0002t0002g0241others(6): Show | 9 | HG01346.hp2 HG02738.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+14121_126+1413 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(5): Show |
A | 10 | a0001c0001t0001g0094a0001c0001t0005g0072a0001c0001t0005g0085others(7): Show | 10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+14119_126+1413 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(7): Show |
A | 5 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14117_126+1413 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(9): Show |
A | 7 | a0001c0001t0001g0044a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01346.hp1 HG02257.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+14115_126+1413 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183043
|
AACACACA others(11): Show |
A | 29 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(26): Show | 29 | HG00621.hp1 HG01081.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+14113_126+1413 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | |||||
| chr4:173183143
|
G | A | 1 | a0001c0003t0002g0247 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.126+14182G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183143 | ||||||
| chr4:173183256
|
C | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+14295C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183256 | ||||||
| chr4:173183281
|
C | CT | 5 | a0001c0001t0005g0085a0001c0001t0011g0071a0001c0006t0001g0073others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+14335dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183281 | |||||
| chr4:173183281
|
CT | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0015g0157others(2): Show | 5 | HG01070.hp2 HG02965.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14335delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183281 | |||||
| chr4:173183478
|
A | AT | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14529dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183478 | |||||
| chr4:173183518
|
A | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14557A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183518 | ||||||
| chr4:173183660
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.126+14699G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183660 | ||||||
| chr4:173183684
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14723C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183684 | ||||||
| chr4:173183688
|
C | T | 3 | a0001c0002t0001g0200a0001c0002t0001g0235a0001c0002t0013g0233 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.126+14727C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183688 | ||||||
| chr4:173183730
|
G | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14769G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183730 | ||||||
| chr4:173183760
|
G | A | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+14799G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183760 | ||||||
| chr4:173183776
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.126+14815A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183776 | ||||||
| chr4:173183781
|
C | G | 1 | a0001c0008t0002g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126+14820C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183781 | ||||||
| chr4:173183781
|
C | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+14820C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183781 | ||||||
| chr4:173183786
|
C | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14825C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183786 | ||||||
| chr4:173183795
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+14834C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183795 | ||||||
| chr4:173183800
|
C | T | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14839C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183800 | ||||||
| chr4:173183801
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.126+14840G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183801 | ||||||
| chr4:173183834
|
CTCCCAGA others(33): Show |
C | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+14897_126+1493 others(44): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183834 | |||||
| chr4:173183851
|
T | C | 20 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(17): Show | 20 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+14890T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183851 | ||||||
| chr4:173183858
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14897C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183858 | ||||||
| chr4:173183882
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14921C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183882 | ||||||
| chr4:173183893
|
C | T | 2 | a0001c0003t0002g0021a0001c0003t0002g0250 | 2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.126+14932C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183893 | ||||||
| chr4:173183900
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14939G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183900 | ||||||
| chr4:173184057
|
C | T | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+15096C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184057 | ||||||
| chr4:173184078
|
G | A | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+15117G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184078 | ||||||
| chr4:173184124
|
G | C | 21 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(18): Show | 21 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+15163G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184124 | ||||||
| chr4:173184132
|
G | A | 9 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15171G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184132 | ||||||
| chr4:173184148
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.126+15187C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184148 | ||||||
| chr4:173184152
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+15191C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184152 | ||||||
| chr4:173184191
|
C | CG | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(4): Show | 7 | HG01952.hp1 HG02027.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+15234dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184191 | |||||
| chr4:173184247
|
C | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+15286C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184247 | ||||||
| chr4:173184271
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+15310G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184271 | ||||||
| chr4:173184386
|
C | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00280.hp2 HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.126+15425C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184386 | ||||||
| chr4:173184405
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.126+15444C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184405 | ||||||
| chr4:173184430
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+15469C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184430 | ||||||
| chr4:173184467
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+15506G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184467 | ||||||
| chr4:173184563
|
GGCTCGGC others(25): Show |
G | 1 | a0001c0002t0001g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+15636_126+1566 others(36): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184563 | |||||
| chr4:173184621
|
A | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+15660A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184621 | ||||||
| chr4:173184630
|
G | A | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.126+15669G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184630 | ||||||
| chr4:173184690
|
G | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+15729G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184690 | ||||||
| chr4:173184743
|
TA | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+15792delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184743 | |||||
| chr4:173184787
|
T | C | 1 | a0004c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+15826T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184787 | ||||||
| chr4:173184865
|
G | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+15904G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184865 | ||||||
| chr4:173184952
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+15991C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184952 | ||||||
| chr4:173185064
|
A | G | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02273.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.126+16103A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185064 | ||||||
| chr4:173185150
|
C | G | 3 | a0001c0002t0001g0186a0001c0002t0001g0190a0001c0002t0001g0198 | 3 | HG01952.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+16189C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185150 | ||||||
| chr4:173185264
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+16303T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185264 | ||||||
| chr4:173185413
|
C | CA | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.126+16466dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173185413 | |||||
| chr4:173185413
|
C | CAA | 9 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0188others(6): Show | 9 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+16465_126+1646 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173185413 | |||||
| chr4:173185512
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+16551C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185512 | ||||||
| chr4:173185599
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.126+16638T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185599 | ||||||
| chr4:173185656
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126+16695A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185656 | ||||||
| chr4:173186083
|
G | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.126+17122G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186083 | ||||||
| chr4:173186148
|
A | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+17187A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186148 | ||||||
| chr4:173186227
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.126+17266A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186227 | ||||||
| chr4:173186278
|
C | A | 7 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(4): Show | 7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+17317C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186278 | ||||||
| chr4:173186278
|
C | T | 1 | a0001c0003t0002g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.126+17317C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186278 | ||||||
| chr4:173186279
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+17318G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186279 | ||||||
| chr4:173186386
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.126+17425T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186386 | ||||||
| chr4:173186420
|
C | T | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.126+17459C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186420 | ||||||
| chr4:173186512
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+17551T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186512 | ||||||
| chr4:173186780
|
C | CT | 19 | a0001c0001t0001g0145a0001c0001t0001g0153a0001c0002t0001g0253others(16): Show | 19 | HG00423.hp1 HG01891.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+17831dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173186780 | |||||
| chr4:173186783
|
T | A | 9 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+17822T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186783 | ||||||
| chr4:173186889
|
C | T | 3 | a0001c0002t0001g0186a0001c0002t0001g0190a0001c0002t0001g0198 | 3 | HG01952.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+17928C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186889 | ||||||
| chr4:173186930
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+17969A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186930 | ||||||
| chr4:173186981
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+18020C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186981 | ||||||
| chr4:173187000
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.126+18039C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187000 | ||||||
| chr4:173187096
|
T | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+18135T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187096 | ||||||
| chr4:173187284
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.126+18323G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187284 | ||||||
| chr4:173187308
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+18347T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187308 | ||||||
| chr4:173187311
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(28): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+18350G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187311 | ||||||
| chr4:173187383
|
G | GA | 15 | a0001c0001t0001g0100a0001c0002t0001g0253a0001c0003t0002g0021others(12): Show | 15 | HG00423.hp1 HG02135.hp2 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+18436dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173187383 | |||||
| chr4:173187383
|
GA | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(23): Show | 26 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+18436delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173187383 | |||||
| chr4:173187450
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+18489A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187450 | ||||||
| chr4:173187603
|
G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+18642G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187603 | ||||||
| chr4:173187778
|
G | T | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+18817G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187778 | ||||||
| chr4:173188048
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+19087T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188048 | ||||||
| chr4:173188460
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+19499A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188460 | ||||||
| chr4:173188471
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+19510C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188471 | ||||||
| chr4:173188513
|
A | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+19552A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188513 | ||||||
| chr4:173188552
|
C | G | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+19591C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188552 | ||||||
| chr4:173188666
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.126+19705C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188666 | ||||||
| chr4:173188691
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+19730C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188691 | ||||||
| chr4:173188739
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.126+19778C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188739 | ||||||
| chr4:173188970
|
C | G | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+20009C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188970 | ||||||
| chr4:173188970
|
C | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.126+20009C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188970 | ||||||
| chr4:173189045
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+20084C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189045 | ||||||
| chr4:173189165
|
C | A | 1 | a0001c0005t0003g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126+20204C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189165 | ||||||
| chr4:173189178
|
A | T | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+20217A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189178 | ||||||
| chr4:173189405
|
A | T | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+20444A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189405 | ||||||
| chr4:173189425
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+20464A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189425 | ||||||
| chr4:173189492
|
T | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+20531T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189492 | ||||||
| chr4:173189506
|
T | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(21): Show | 24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+20545T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189506 | ||||||
| chr4:173189724
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+20763T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189724 | ||||||
| chr4:173189746
|
T | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+20785T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189746 | ||||||
| chr4:173189994
|
G | GT | 8 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(5): Show | 8 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+21046dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173189994 | |||||
| chr4:173189994
|
G | T | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+21033G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189994 | ||||||
| chr4:173189994
|
GT | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(24): Show | 27 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+21046delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173189994 | |||||
| chr4:173190037
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+21076G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190037 | ||||||
| chr4:173190088
|
T | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(14): Show | 17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+21127T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190088 | ||||||
| chr4:173190103
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(14): Show | 17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+21142T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190103 | ||||||
| chr4:173190223
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+21262G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190223 | ||||||
| chr4:173190312
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+21351C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190312 | ||||||
| chr4:173190529
|
G | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+21568G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190529 | ||||||
| chr4:173190542
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+21581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190542 | ||||||
| chr4:173190888
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0146 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.126+21927C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190888 | ||||||
| chr4:173190906
|
T | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+21945T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190906 | ||||||
| chr4:173190908
|
G | T | 1 | a0001c0001t0004g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+21947G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190908 | ||||||
| chr4:173190936
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.126+21975T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190936 | ||||||
| chr4:173191046
|
G | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+22085G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191046 | ||||||
| chr4:173191063
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.126+22102G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191063 | ||||||
| chr4:173191063
|
GA | G | 8 | a0001c0001t0001g0053a0001c0002t0001g0173a0001c0002t0001g0174others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+22114delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191063 | |||||
| chr4:173191063
|
GAA | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+22113_126+2211 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191063 | |||||
| chr4:173191124
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+22163A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191124 | ||||||
| chr4:173191209
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+22248A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191209 | ||||||
| chr4:173191227
|
T | TG | 19 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(16): Show | 19 | HG01257.hp1 HG01346.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+22274dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191227 | |||||
| chr4:173191230
|
G | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+22269G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191230 | ||||||
| chr4:173191359
|
C | T | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22398C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191359 | ||||||
| chr4:173191385
|
G | A | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22424G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191385 | ||||||
| chr4:173191392
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+22431C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191392 | ||||||
| chr4:173191439
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(22): Show | 25 | HG01081.hp2 HG01346.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+22478G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191439 | ||||||
| chr4:173191487
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22526G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191487 | ||||||
| chr4:173191577
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+22616G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191577 | ||||||
| chr4:173192058
|
C | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+23097C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192058 | ||||||
| chr4:173192083
|
T | C | 1 | a0001c0002t0001g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.126+23122T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192083 | ||||||
| chr4:173192212
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0058others(1): Show | 4 | HG00280.hp2 HG01099.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+23251A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192212 | ||||||
| chr4:173192223
|
C | T | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.126+23262C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192223 | ||||||
| chr4:173192308
|
C | A | 1 | a0001c0001t0004g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.126+23347C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192308 | ||||||
| chr4:173192475
|
A | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+23514A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192475 | ||||||
| chr4:173192614
|
G | A | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+23653G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192614 | ||||||
| chr4:173192938
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.126+23977C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192938 | ||||||
| chr4:173193013
|
G | C | 1 | a0001c0002t0001g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+24052G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193013 | ||||||
| chr4:173193386
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+24425G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193386 | ||||||
| chr4:173193428
|
C | T | 2 | a0001c0002t0006g0170a0001c0002t0006g0171 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.126+24467C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193428 | ||||||
| chr4:173193493
|
T | A | 1 | a0001c0001t0005g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+24532T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193493 | ||||||
| chr4:173193504
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+24543C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193504 | ||||||
| chr4:173193563
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0125 | 3 | NA18966.hp1 NA18969.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.126+24602A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193563 | ||||||
| chr4:173194244
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0153 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.126+25283A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194244 | ||||||
| chr4:173194272
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+25311G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194272 | ||||||
| chr4:173194308
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | HG01192.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.126+25347G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194308 | ||||||
| chr4:173194405
|
T | C | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+25444T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194405 | ||||||
| chr4:173194579
|
C | A | 2 | a0003c0013t0001g0175a0004c0011t0002g0180 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+25618C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194579 | ||||||
| chr4:173194580
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+25619G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194580 | ||||||
| chr4:173194776
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0032others(26): Show | 29 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+25815C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194776 | ||||||
| chr4:173194778
|
T | A | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+25817T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194778 | ||||||
| chr4:173194793
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+25832C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194793 | ||||||
| chr4:173195284
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+26323C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195284 | ||||||
| chr4:173195304
|
A | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+26343A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195304 | ||||||
| chr4:173195379
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126+26418G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195379 | ||||||
| chr4:173195405
|
G | C | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+26444G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195405 | ||||||
| chr4:173195461
|
G | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(27): Show | 30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+26500G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195461 | ||||||
| chr4:173195873
|
T | G | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02273.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.126+26912T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195873 | ||||||
| chr4:173196127
|
A | AT | 52 | a0001c0001t0001g0064a0001c0001t0001g0108a0001c0001t0001g0146others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.126+27181dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173196127 | |||||
| chr4:173196155
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+27194C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196155 | ||||||
| chr4:173196252
|
G | A | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+27291G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196252 | ||||||
| chr4:173196269
|
C | T | 7 | a0001c0002t0001g0203a0001c0002t0001g0207a0001c0002t0001g0216others(4): Show | 7 | HG01074.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+27308C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196269 | ||||||
| chr4:173196325
|
A | G | 2 | a0003c0013t0001g0175a0004c0011t0002g0180 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+27364A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196325 | ||||||
| chr4:173196732
|
C | T | 2 | a0001c0002t0001g0206a0001c0002t0001g0219 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.126+27771C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196732 | ||||||
| chr4:173196950
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(27): Show | 30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+27989C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196950 | ||||||
| chr4:173197063
|
C | CT | 137 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.126+28122dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197063
|
C | CTT | 11 | a0001c0001t0001g0002a0001c0001t0014g0057a0001c0002t0002g0020others(8): Show | 11 | HG02273.hp2 HG02809.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+28121_126+2812 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197063
|
C | CTTT | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(45): Show | 48 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+28120_126+2812 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197063
|
CT | C | 6 | a0001c0002t0001g0014a0001c0002t0001g0185a0001c0002t0006g0170others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+28122delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197063
|
CTTTT | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(15): Show | 18 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+28119_126+2812 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197063
|
CTTTTT | C | 14 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(11): Show | 14 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+28118_126+2812 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | |||||
| chr4:173197137
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+28176A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197137 | ||||||
| chr4:173197298
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.126+28337G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197298 | ||||||
| chr4:173197358
|
TG | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+28398delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197358 | ||||||
| chr4:173197379
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126+28418G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197379 | ||||||
| chr4:173197434
|
TAATC | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+28477_126+2848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197434 | |||||
| chr4:173197507
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+28546A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197507 | ||||||
| chr4:173197519
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.126+28558T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197519 | ||||||
| chr4:173197898
|
G | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+28937G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197898 | ||||||
| chr4:173198065
|
CT | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(61): Show | 64 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.126+29116delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198065 | |||||
| chr4:173198065
|
CTT | C | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+29115_126+2911 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198065 | |||||
| chr4:173198069
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+29108T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198069 | ||||||
| chr4:173198216
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.126+29255T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198216 | ||||||
| chr4:173198226
|
A | AT | 22 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0079others(19): Show | 22 | HG01081.hp2 HG01884.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+29280dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | |||||
| chr4:173198226
|
A | ATT | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(51): Show | 54 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+29279_126+2928 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | |||||
| chr4:173198226
|
A | ATTT | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.126+29278_126+2928 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | |||||
| chr4:173198226
|
A | ATTTT | 10 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0039others(7): Show | 10 | HG01099.hp1 HG01993.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+29277_126+2928 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | |||||
| chr4:173198265
|
T | C | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+29304T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198265 | ||||||
| chr4:173198281
|
G | A | 1 | a0001c0008t0002g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126+29320G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198281 | ||||||
| chr4:173198290
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+29329G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198290 | ||||||
| chr4:173198319
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+29358C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198319 | ||||||
| chr4:173198330
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+29369G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198330 | ||||||
| chr4:173198364
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+29403G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198364 | ||||||
| chr4:173198370
|
G | T | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02273.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.126+29409G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198370 | ||||||
| chr4:173198417
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126+29456A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198417 | ||||||
| chr4:173198458
|
T | A | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+29497T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198458 | ||||||
| chr4:173198526
|
A | G | 9 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+29565A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198526 | ||||||
| chr4:173198578
|
C | G | 1 | a0001c0001t0002g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+29617C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198578 | ||||||
| chr4:173198609
|
A | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+29648A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198609 | ||||||
| chr4:173198711
|
G | C | 10 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+29750G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198711 | ||||||
| chr4:173198773
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.126+29812G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198773 | ||||||
| chr4:173199110
|
A | T | 1 | a0001c0001t0005g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+30149A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199110 | ||||||
| chr4:173199124
|
C | A | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+30163C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199124 | ||||||
| chr4:173199131
|
G | A | 3 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+30170G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199131 | ||||||
| chr4:173199133
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126+30172G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199133 | ||||||
| chr4:173199203
|
G | A | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+30242G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199203 | ||||||
| chr4:173199352
|
C | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+30391C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199352 | ||||||
| chr4:173199401
|
G | A | 1 | a0001c0002t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.126+30440G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199401 | ||||||
| chr4:173199479
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.126+30518T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199479 | ||||||
| chr4:173199499
|
G | A | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+30538G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199499 | ||||||
| chr4:173199755
|
C | T | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+30794C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199755 | ||||||
| chr4:173199925
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0113a0001c0001t0001g0126others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+30964T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199925 | ||||||
| chr4:173199968
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+31007T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199968 | ||||||
| chr4:173199977
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.126+31016A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199977 | ||||||
| chr4:173200195
|
T | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+31234T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200195 | ||||||
| chr4:173200450
|
T | TA | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+31501dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173200450 | |||||
| chr4:173200450
|
TA | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+31501delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173200450 | |||||
| chr4:173200599
|
C | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+31638C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200599 | ||||||
| chr4:173200773
|
C | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+31812C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200773 | ||||||
| chr4:173201024
|
T | A | 1 | a0001c0002t0001g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+32063T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201024 | ||||||
| chr4:173201105
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+32144A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201105 | ||||||
| chr4:173201148
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+32187C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201148 | ||||||
| chr4:173201238
|
AAT | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+32279_126+3228 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173201238 | |||||
| chr4:173201286
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.126+32325T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201286 | ||||||
| chr4:173201405
|
A | G | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+32444A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201405 | ||||||
| chr4:173201439
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.126+32478T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201439 | ||||||
| chr4:173201469
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+32508A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201469 | ||||||
| chr4:173201654
|
A | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+32693A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201654 | ||||||
| chr4:173201994
|
A | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+33033A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201994 | ||||||
| chr4:173202033
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+33072A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202033 | ||||||
| chr4:173202156
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.126+33195G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202156 | ||||||
| chr4:173202293
|
G | C | 2 | a0001c0002t0001g0188a0001c0002t0002g0192 | 2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.126+33332G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202293 | ||||||
| chr4:173202366
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0265 | 2 | NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.126+33405A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202366 | ||||||
| chr4:173202526
|
A | T | 1 | a0001c0001t0004g0112 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.126+33565A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202526 | ||||||
| chr4:173202640
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.126+33679A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202640 | ||||||
| chr4:173202821
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.126+33860A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202821 | ||||||
| chr4:173202841
|
G | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+33880G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202841 | ||||||
| chr4:173203016
|
AT | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(32): Show | 35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+34068delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173203016 | |||||
| chr4:173203017
|
T | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+34056T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203017 | ||||||
| chr4:173203046
|
G | A | 1 | a0004c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+34085G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203046 | ||||||
| chr4:173203057
|
C | G | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+34096C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203057 | ||||||
| chr4:173203126
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0005g0086 | 3 | HG02145.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+34165C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203126 | ||||||
| chr4:173203239
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.126+34278G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203239 | ||||||
| chr4:173203243
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+34282G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203243 | ||||||
| chr4:173203283
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+34322C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203283 | ||||||
| chr4:173203298
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126+34337A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203298 | ||||||
| chr4:173203324
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+34363T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203324 | ||||||
| chr4:173203327
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.126+34366G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203327 | ||||||
| chr4:173203342
|
C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+34381C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203342 | ||||||
| chr4:173203456
|
A | C | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+34495A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203456 | ||||||
| chr4:173203479
|
A | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+34518A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203479 | ||||||
| chr4:173203556
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+34595A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203556 | ||||||
| chr4:173203653
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+34692G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203653 | ||||||
| chr4:173203826
|
TTAAA | T | 7 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(4): Show | 7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+34869_126+3487 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173203826 | |||||
| chr4:173203964
|
A | G | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+35003A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203964 | ||||||
| chr4:173203979
|
C | T | 3 | a0001c0002t0001g0199a0001c0002t0001g0220a0001c0003t0002g0237 | 3 | HG00558.hp1 NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.126+35018C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203979 | ||||||
| chr4:173203982
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+35021G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203982 | ||||||
| chr4:173204282
|
C | T | 1 | a0001c0002t0001g0194 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.126+35321C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204282 | ||||||
| chr4:173204524
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+35563T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204524 | ||||||
| chr4:173204749
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+35788G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204749 | ||||||
| chr4:173204793
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.126+35832T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204793 | ||||||
| chr4:173204794
|
A | G | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+35833A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204794 | ||||||
| chr4:173204832
|
T | C | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+35871T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204832 | ||||||
| chr4:173204986
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126+36025A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204986 | ||||||
| chr4:173205097
|
C | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+36136C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205097 | ||||||
| chr4:173205110
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.126+36149G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205110 | ||||||
| chr4:173205260
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.126+36299T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205260 | ||||||
| chr4:173205306
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+36345G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205306 | ||||||
| chr4:173205676
|
GGGTCTGA others(13): Show |
G | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+36737_126+3675 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173205676 | |||||
| chr4:173205785
|
G | C | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+36824G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205785 | ||||||
| chr4:173205813
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.126+36852C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205813 | ||||||
| chr4:173205880
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.126+36919G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205880 | ||||||
| chr4:173206274
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+37313G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206274 | ||||||
| chr4:173206285
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+37324A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206285 | ||||||
| chr4:173206326
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0133 | 2 | NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.126+37365T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206326 | ||||||
| chr4:173206474
|
A | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(27): Show | 30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+37513A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206474 | ||||||
| chr4:173206556
|
G | C | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+37595G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206556 | ||||||
| chr4:173206765
|
T | G | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+37804T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206765 | ||||||
| chr4:173206903
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+37942G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206903 | ||||||
| chr4:173207102
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+38141G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207102 | ||||||
| chr4:173207364
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+38403A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207364 | ||||||
| chr4:173207514
|
C | T | 20 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(17): Show | 20 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+38553C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207514 | ||||||
| chr4:173207619
|
T | A | 2 | a0001c0001t0004g0115a0001c0001t0004g0122 | 2 | HG01952.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.126+38658T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207619 | ||||||
| chr4:173207762
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.126+38801T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207762 | ||||||
| chr4:173208320
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+39359C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208320 | ||||||
| chr4:173208488
|
A | G | 1 | a0001c0002t0001g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127-39492A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208488 | ||||||
| chr4:173208545
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.127-39435C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208545 | ||||||
| chr4:173208589
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.127-39391A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208589 | ||||||
| chr4:173208633
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-39347G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208633 | ||||||
| chr4:173208651
|
T | G | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-39329T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208651 | ||||||
| chr4:173208770
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-39210C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208770 | ||||||
| chr4:173208807
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-39173A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208807 | ||||||
| chr4:173209054
|
A | G | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-38926A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209054 | ||||||
| chr4:173209114
|
T | G | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.127-38866T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209114 | ||||||
| chr4:173209257
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-38723C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209257 | ||||||
| chr4:173209341
|
G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(27): Show | 30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-38639G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209341 | ||||||
| chr4:173209352
|
T | C | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-38628T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209352 | ||||||
| chr4:173209435
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-38545G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209435 | ||||||
| chr4:173209521
|
T | G | 1 | a0001c0002t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-38459T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209521 | ||||||
| chr4:173209716
|
C | G | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-38264C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209716 | ||||||
| chr4:173210007
|
C | T | 2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG02273.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.127-37973C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210007 | ||||||
| chr4:173210133
|
CA | C | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37840delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173210133 | |||||
| chr4:173210141
|
G | GA | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-37826dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173210141 | |||||
| chr4:173210165
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-37815T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210165 | ||||||
| chr4:173210194
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-37786G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210194 | ||||||
| chr4:173210296
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.127-37684G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210296 | ||||||
| chr4:173210305
|
G | T | 1 | a0001c0002t0001g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127-37675G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210305 | ||||||
| chr4:173210323
|
G | A | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-37657G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210323 | ||||||
| chr4:173210520
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.127-37460T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210520 | ||||||
| chr4:173210630
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-37350A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210630 | ||||||
| chr4:173210647
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-37333G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210647 | ||||||
| chr4:173210710
|
G | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37270G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210710 | ||||||
| chr4:173210720
|
C | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37260C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210720 | ||||||
| chr4:173210758
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-37222T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210758 | ||||||
| chr4:173210875
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.127-37105T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210875 | ||||||
| chr4:173210993
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-36987G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210993 | ||||||
| chr4:173210995
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.127-36985G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210995 | ||||||
| chr4:173211026
|
C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.127-36954C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211026 | ||||||
| chr4:173211059
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.127-36921A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211059 | ||||||
| chr4:173211259
|
C | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36721C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211259 | ||||||
| chr4:173211273
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-36707C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211273 | ||||||
| chr4:173211288
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36692G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211288 | ||||||
| chr4:173211299
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-36681C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211299 | ||||||
| chr4:173211337
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-36643G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211337 | ||||||
| chr4:173211468
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-36512C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211468 | ||||||
| chr4:173211489
|
C | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36491C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211489 | ||||||
| chr4:173211682
|
A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-36298A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211682 | ||||||
| chr4:173211834
|
T | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-36146T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211834 | ||||||
| chr4:173212486
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-35494C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212486 | ||||||
| chr4:173212628
|
C | CT | 26 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(23): Show | 26 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-35339dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173212628 | |||||
| chr4:173212628
|
CT | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.127-35339delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173212628 | |||||
| chr4:173212683
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-35297G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212683 | ||||||
| chr4:173212707
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-35273A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212707 | ||||||
| chr4:173212734
|
CAT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.127-35245_127-3524 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212734 | ||||||
| chr4:173212819
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-35161C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212819 | ||||||
| chr4:173212843
|
A | C | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-35137A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212843 | ||||||
| chr4:173213117
|
G | A | 3 | a0001c0004t0001g0006a0001c0005t0003g0093a0001c0005t0003g0095 | 3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127-34863G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213117 | ||||||
| chr4:173213228
|
T | TG | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-34752_127-3475 others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213228 | ||||||
| chr4:173213241
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-34739C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213241 | ||||||
| chr4:173213277
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127-34703C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213277 | ||||||
| chr4:173213381
|
A | G | 3 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0236 | 3 | HG01981.hp1 HG02056.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.127-34599A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213381 | ||||||
| chr4:173213533
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.127-34447G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213533 | ||||||
| chr4:173213670
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-34310G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213670 | ||||||
| chr4:173214136
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-33844T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214136 | ||||||
| chr4:173214143
|
AT | A | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-33835delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214143 | |||||
| chr4:173214288
|
T | TA | 32 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0039others(29): Show | 32 | HG00621.hp1 HG01192.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-33678dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | |||||
| chr4:173214288
|
T | TAA | 10 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(7): Show | 10 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-33679_127-3367 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | |||||
| chr4:173214288
|
TA | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-33678delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | |||||
| chr4:173214644
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-33336A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214644 | ||||||
| chr4:173214656
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-33324C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214656 | ||||||
| chr4:173214802
|
A | AT | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-33163dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | |||||
| chr4:173214802
|
AT | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.127-33163delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | |||||
| chr4:173214802
|
ATT | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0069others(11): Show | 14 | HG00423.hp2 HG01256.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-33164_127-3316 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | |||||
| chr4:173214980
|
T | C | 3 | a0001c0002t0001g0200a0001c0002t0001g0235a0001c0002t0013g0233 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-33000T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214980 | ||||||
| chr4:173215232
|
C | CT | 59 | a0001c0001t0001g0032a0001c0001t0002g0033a0001c0001t0002g0034others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.127-32732dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173215232 | |||||
| chr4:173215235
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-32745T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215235 | ||||||
| chr4:173215236
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.127-32744T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215236 | ||||||
| chr4:173215299
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-32681C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215299 | ||||||
| chr4:173215395
|
T | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-32585T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215395 | ||||||
| chr4:173215416
|
A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-32564A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215416 | ||||||
| chr4:173215482
|
G | A | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-32498G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215482 | ||||||
| chr4:173215566
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-32414A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215566 | ||||||
| chr4:173215570
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127-32410G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215570 | ||||||
| chr4:173215605
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-32375C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215605 | ||||||
| chr4:173215606
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-32374G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215606 | ||||||
| chr4:173215708
|
A | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-32272A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215708 | ||||||
| chr4:173215801
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-32179C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215801 | ||||||
| chr4:173215848
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-32132G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215848 | ||||||
| chr4:173215966
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-32014A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215966 | ||||||
| chr4:173216032
|
G | A | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31948G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216032 | ||||||
| chr4:173216109
|
C | A | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-31871C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216109 | ||||||
| chr4:173216147
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-31833G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216147 | ||||||
| chr4:173216165
|
A | G | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31815A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216165 | ||||||
| chr4:173216362
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.127-31618A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216362 | ||||||
| chr4:173216372
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-31608G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216372 | ||||||
| chr4:173216372
|
G | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(32): Show | 35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-31608G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216372 | ||||||
| chr4:173216589
|
A | G | 1 | a0001c0002t0001g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-31391A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216589 | ||||||
| chr4:173216619
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-31361G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216619 | ||||||
| chr4:173216654
|
G | A | 1 | a0001c0001t0004g0112 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.127-31326G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216654 | ||||||
| chr4:173216706
|
C | CAT | 23 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(20): Show | 23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-31253_127-3125 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATAT | 4 | a0001c0001t0001g0030a0001c0001t0002g0031a0001c0001t0002g0035others(1): Show | 4 | NA18964.hp1 NA18970.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31255_127-3125 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(3): Show |
1 | a0001c0002t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-31261_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(17): Show |
5 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0195others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(28): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(19): Show |
2 | a0001c0002t0001g0189a0001c0002t0001g0194 | 2 | HG02897.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(30): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(21): Show |
1 | a0001c0002t0001g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(32): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(25): Show |
1 | a0001c0002t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.127-31252_127-3125 others(36): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216706
|
C | CATATATA others(27): Show |
1 | a0001c0002t0001g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(38): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | |||||
| chr4:173216718
|
T | A | 14 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(11): Show | 14 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-31262T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216718 | ||||||
| chr4:173216719
|
A | ATT | 5 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0011g0071others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-31260_127-3125 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216719 | |||||
| chr4:173216721
|
A | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31259A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216721 | ||||||
| chr4:173216723
|
A | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31257A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216723 | ||||||
| chr4:173216725
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.127-31254_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216725 | |||||
| chr4:173216725
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0131 | 2 | HG02083.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.127-31254_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216725 | |||||
| chr4:173216725
|
A | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31255A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216725 | ||||||
| chr4:173216727
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-31252_127-3125 others(25): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0003g0078a0001c0001t0003g0083a0001c0002t0001g0187 | 3 | HG02615.hp2 NA18970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(29): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(28): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0080 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0011g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(27): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(20): Show |
2 | a0001c0002t0001g0183a0001c0004t0001g0084 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(31): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(12): Show |
2 | a0001c0004t0001g0076a0001c0004t0001g0077 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(23): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(9): Show |
3 | a0001c0004t0001g0006a0001c0005t0003g0093a0001c0005t0003g0095 | 3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(2): Show |
12 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(9): Show | 12 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0014g0057others(2): Show | 5 | HG02273.hp2 HG02738.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(1): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG01257.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(3): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0058others(4): Show | 7 | HG00280.hp2 HG01099.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(4): Show |
8 | a0001c0001t0001g0052a0001c0001t0001g0094a0001c0001t0001g0096others(5): Show | 8 | HG01257.hp2 HG01346.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(5): Show |
3 | a0001c0001t0001g0046a0001c0001t0001g0106a0001c0001t0001g0266 | 3 | HG00597.hp2 HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(6): Show |
2 | a0001c0001t0001g0128a0001c0001t0001g0142 | 2 | HG02056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATATTT others(7): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0109 | 2 | HG00423.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTT | 5 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0102others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(1): Show |
10 | a0001c0002t0001g0199a0001c0002t0001g0206a0001c0002t0001g0220others(7): Show | 10 | HG00558.hp1 HG00597.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(2): Show |
28 | a0001c0002t0001g0016a0001c0002t0001g0018a0001c0002t0001g0179others(25): Show | 28 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(3): Show |
25 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(22): Show | 25 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0141 | 2 | HG01934.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(5): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0001g0119others(6): Show | 9 | HG02683.hp1 HG02717.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(6): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0162 | 2 | HG02135.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATATTTTT others(7): Show |
1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0013a0001c0001t0001g0132a0001c0002t0001g0211others(6): Show | 9 | HG01928.hp2 HG02080.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-31242_127-3123 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATTTTTTT others(3): Show |
27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0064others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-31243_127-3123 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATTTTTTT others(4): Show |
12 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0124others(9): Show | 12 | HG01071.hp1 HG01106.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-31244_127-3123 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0155 | 2 | HG02027.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.127-31245_127-3123 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | |||||
| chr4:173216727
|
A | T | 14 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0004g0122others(11): Show | 14 | HG01952.hp2 HG02083.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-31253A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216727 | ||||||
| chr4:173216728
|
T | TATATATA others(18): Show |
2 | a0001c0002t0001g0186a0001c0002t0001g0198 | 2 | HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(29): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216728 | ||||||
| chr4:173216728
|
T | TATATATA others(22): Show |
2 | a0001c0002t0001g0190a0001c0002t0001g0191 | 2 | HG01952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(33): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216728 | ||||||
| chr4:173216729
|
T | A | 2 | a0001c0002t0001g0188a0001c0002t0002g0192 | 2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.127-31251T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216729 | ||||||
| chr4:173216767
|
G | C | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-31213G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216767 | ||||||
| chr4:173216799
|
C | T | 22 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0253others(19): Show | 22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-31181C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216799 | ||||||
| chr4:173216800
|
G | T | 3 | a0001c0002t0001g0200a0001c0002t0001g0235a0001c0002t0013g0233 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-31180G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216800 | ||||||
| chr4:173216843
|
G | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-31137G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216843 | ||||||
| chr4:173216856
|
G | A | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-31124G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216856 | ||||||
| chr4:173217168
|
A | T | 1 | a0001c0002t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-30812A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217168 | ||||||
| chr4:173217621
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-30359A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217621 | ||||||
| chr4:173217625
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-30355T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217625 | ||||||
| chr4:173217630
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0087 | 3 | HG02055.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.127-30350A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217630 | ||||||
| chr4:173217716
|
T | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.127-30264T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217716 | ||||||
| chr4:173217724
|
A | G | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.127-30256A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217724 | ||||||
| chr4:173217871
|
A | G | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-30109A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217871 | ||||||
| chr4:173217975
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.127-30005C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217975 | ||||||
| chr4:173218024
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-29956G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218024 | ||||||
| chr4:173218048
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.127-29932G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218048 | ||||||
| chr4:173218096
|
C | G | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-29884C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218096 | ||||||
| chr4:173218138
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-29842A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218138 | ||||||
| chr4:173218469
|
GTTTCC | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.127-29507_127-2950 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218469 | |||||
| chr4:173218604
|
C | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(32): Show | 35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-29376C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218604 | ||||||
| chr4:173218976
|
TA | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-28997delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218976 | |||||
| chr4:173218983
|
AT | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(27): Show | 30 | HG00621.hp1 HG01192.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-28987delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218983 | |||||
| chr4:173219048
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-28932G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219048 | ||||||
| chr4:173219176
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-28804T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219176 | ||||||
| chr4:173219176
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-28804T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219176 | ||||||
| chr4:173219301
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0133 | 3 | HG02040.hp1 NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.127-28679T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219301 | ||||||
| chr4:173219360
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-28620A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219360 | ||||||
| chr4:173219701
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(31): Show | 34 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.127-28279T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219701 | ||||||
| chr4:173219751
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.127-28229C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219751 | ||||||
| chr4:173219764
|
A | AT | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-28208dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173219764 | |||||
| chr4:173219879
|
A | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-28101A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219879 | ||||||
| chr4:173220371
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.127-27609T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220371 | ||||||
| chr4:173220430
|
C | A | 1 | a0001c0001t0015g0157 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.127-27550C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220430 | ||||||
| chr4:173220430
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00280.hp2 HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.127-27550C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220430 | ||||||
| chr4:173220449
|
G | A | 1 | a0001c0005t0003g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-27531G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220449 | ||||||
| chr4:173220502
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.127-27478A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220502 | ||||||
| chr4:173220503
|
A | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 81 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-27477A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220503 | ||||||
| chr4:173220608
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-27372G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220608 | ||||||
| chr4:173220705
|
C | T | 2 | a0001c0002t0001g0189a0001c0002t0001g0238 | 2 | NA18986.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.127-27275C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220705 | ||||||
| chr4:173220748
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-27232G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220748 | ||||||
| chr4:173220827
|
G | C | 1 | a0001c0008t0002g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.127-27153G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220827 | ||||||
| chr4:173220870
|
A | G | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-27110A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220870 | ||||||
| chr4:173220899
|
C | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-27081C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220899 | ||||||
| chr4:173220916
|
G | A | 1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-27064G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220916 | ||||||
| chr4:173220938
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-27042T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220938 | ||||||
| chr4:173220951
|
G | A | 1 | a0001c0002t0002g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-27029G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220951 | ||||||
| chr4:173220954
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-27026A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220954 | ||||||
| chr4:173221302
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-26678A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221302 | ||||||
| chr4:173221423
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-26557G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221423 | ||||||
| chr4:173221498
|
G | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0005t0001g0099others(3): Show | 6 | HG01346.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-26482G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221498 | ||||||
| chr4:173221723
|
A | G | 51 | a0001c0001t0001g0266a0001c0002t0001g0016a0001c0002t0001g0017others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.127-26257A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221723 | ||||||
| chr4:173221816
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-26164T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221816 | ||||||
| chr4:173221891
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-26089C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221891 | ||||||
| chr4:173222130
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 42 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-25850C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222130 | ||||||
| chr4:173222184
|
A | G | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-25796A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222184 | ||||||
| chr4:173222329
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-25651A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222329 | ||||||
| chr4:173222607
|
AG | A | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-25372delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222607 | ||||||
| chr4:173222845
|
A | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-25135A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222845 | ||||||
| chr4:173222849
|
A | G | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-25131A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222849 | ||||||
| chr4:173222880
|
A | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-25100A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222880 | ||||||
| chr4:173222927
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-25053A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222927 | ||||||
| chr4:173223038
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24942G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223038 | ||||||
| chr4:173223056
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-24924A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223056 | ||||||
| chr4:173223478
|
G | GTAATAA | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.127-24498_127-2449 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173223478 | |||||
| chr4:173223574
|
C | T | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-24406C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223574 | ||||||
| chr4:173223598
|
G | A | 2 | a0001c0003t0002g0176a0001c0003t0002g0181 | 2 | HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.127-24382G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223598 | ||||||
| chr4:173223636
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24344C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223636 | ||||||
| chr4:173223878
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-24102T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223878 | ||||||
| chr4:173223898
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24082T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223898 | ||||||
| chr4:173223972
|
T | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-24008T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223972 | ||||||
| chr4:173224007
|
C | CT | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 41 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-23964dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173224007 | |||||
| chr4:173224241
|
G | A | 26 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(23): Show | 26 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-23739G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224241 | ||||||
| chr4:173224480
|
T | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.127-23500T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224480 | ||||||
| chr4:173224734
|
C | T | 45 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0002t0001g0016others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.127-23246C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224734 | ||||||
| chr4:173224738
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.127-23242C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224738 | ||||||
| chr4:173224740
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-23240C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224740 | ||||||
| chr4:173224741
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-23239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224741 | ||||||
| chr4:173224753
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-23227C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224753 | ||||||
| chr4:173224779
|
G | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.127-23201G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224779 | ||||||
| chr4:173224789
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.127-23191G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224789 | ||||||
| chr4:173224795
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0130 | 2 | NA19010.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.127-23185G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224795 | ||||||
| chr4:173224809
|
C | G | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-23171C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224809 | ||||||
| chr4:173224821
|
G | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-23159G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224821 | ||||||
| chr4:173224828
|
C | G | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0003t0002g0169 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.127-23152C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224828 | ||||||
| chr4:173224840
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0002g0040 | 3 | HG01192.hp1 HG01943.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.127-23140G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224840 | ||||||
| chr4:173224874
|
G | T | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-23106G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224874 | ||||||
| chr4:173224875
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0064others(52): Show | 55 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.127-23105C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224875 | ||||||
| chr4:173224879
|
G | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(22): Show | 25 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-23101G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224879 | ||||||
| chr4:173224883
|
C | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-23097C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224883 | ||||||
| chr4:173224884
|
G | A | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-23096G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224884 | ||||||
| chr4:173224885
|
C | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(22): Show | 25 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-23095C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224885 | ||||||
| chr4:173224888
|
G | A | 1 | a0001c0002t0001g0226 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.127-23092G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224888 | ||||||
| chr4:173224966
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127-23014A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224966 | ||||||
| chr4:173224979
|
C | A | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-23001C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224979 | ||||||
| chr4:173224984
|
T | C | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22996T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224984 | ||||||
| chr4:173224992
|
A | G | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22988A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224992 | ||||||
| chr4:173224994
|
G | C | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22986G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224994 | ||||||
| chr4:173225018
|
A | AAATAAT | 7 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0081others(4): Show | 7 | HG02615.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22934_127-2292 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
A | AAATAATA others(2): Show |
4 | a0001c0001t0003g0080a0001c0006t0001g0073a0001c0006t0001g0074others(1): Show | 4 | HG01081.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-22937_127-2292 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
A | AAATAATA others(5): Show |
2 | a0001c0001t0003g0078a0001c0001t0005g0072 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.127-22940_127-2292 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
A | AAATAATA others(8): Show |
2 | a0001c0001t0005g0085a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.127-22943_127-2292 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
A | AAATAATA others(11): Show |
2 | a0001c0001t0011g0071a0001c0002t0011g0208 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-22946_127-2292 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
AAAT | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(46): Show | 49 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-22931_127-2292 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
AAATAAT | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.127-22934_127-2292 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225018
|
AAATAATA others(2): Show |
A | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22937_127-2292 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | |||||
| chr4:173225046
|
AATAATT | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG02451.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-22924_127-2291 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225046 | |||||
| chr4:173225049
|
A | AATT | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-22928_127-2292 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225049 | |||||
| chr4:173225148
|
C | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.127-22832C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225148 | ||||||
| chr4:173225333
|
A | G | 3 | a0001c0002t0009g0244a0001c0002t0009g0245a0003c0013t0001g0175 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-22647A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225333 | ||||||
| chr4:173225497
|
A | G | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-22483A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225497 | ||||||
| chr4:173225504
|
G | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-22476G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225504 | ||||||
| chr4:173225579
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.127-22401G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225579 | ||||||
| chr4:173225621
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.127-22359T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225621 | ||||||
| chr4:173225633
|
C | T | 3 | a0001c0002t0001g0200a0001c0002t0001g0235a0001c0002t0013g0233 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-22347C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225633 | ||||||
| chr4:173225745
|
G | A | 1 | a0007c0010t0003g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-22235G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225745 | ||||||
| chr4:173226189
|
C | G | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-21791C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226189 | ||||||
| chr4:173226208
|
C | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.127-21772C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226208 | ||||||
| chr4:173226210
|
A | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-21770A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226210 | ||||||
| chr4:173226281
|
C | G | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-21699C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226281 | ||||||
| chr4:173226357
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-21623C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226357 | ||||||
| chr4:173226392
|
T | A | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-21588T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226392 | ||||||
| chr4:173226426
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-21554C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226426 | ||||||
| chr4:173226874
|
T | C | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-21106T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226874 | ||||||
| chr4:173226926
|
A | T | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-21054A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226926 | ||||||
| chr4:173226960
|
A | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 10 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-21020A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226960 | ||||||
| chr4:173227234
|
A | G | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-20746A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227234 | ||||||
| chr4:173227417
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.127-20563C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227417 | ||||||
| chr4:173227461
|
A | G | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-20519A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227461 | ||||||
| chr4:173227497
|
A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-20483A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227497 | ||||||
| chr4:173227564
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-20416C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227564 | ||||||
| chr4:173227572
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-20408C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227572 | ||||||
| chr4:173227590
|
C | G | 27 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(24): Show | 27 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-20390C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227590 | ||||||
| chr4:173227786
|
A | G | 8 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-20194A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227786 | ||||||
| chr4:173227794
|
CTG | C | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-20182_127-2018 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227794 | |||||
| chr4:173227812
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-20168T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227812 | ||||||
| chr4:173227813
|
T | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | NA18946.hp1 NA18979.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-20167T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227813 | ||||||
| chr4:173227822
|
T | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 43 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-20158T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227822 | ||||||
| chr4:173227823
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-20157C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227823 | ||||||
| chr4:173227848
|
G | GT | 5 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0118others(2): Show | 5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-20126dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227848 | |||||
| chr4:173227858
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-20122T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227858 | ||||||
| chr4:173227895
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-20085C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227895 | ||||||
| chr4:173227910
|
C | T | 1 | a0001c0002t0011g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-20070C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227910 | ||||||
| chr4:173227960
|
A | G | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-20020A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227960 | ||||||
| chr4:173227984
|
GTCATGTG others(3): Show |
G | 1 | a0001c0002t0001g0210 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.127-19993_127-1998 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227984 | |||||
| chr4:173228141
|
G | A | 4 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0011g0071others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-19839G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228141 | ||||||
| chr4:173228150
|
A | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-19830A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228150 | ||||||
| chr4:173228212
|
G | T | 41 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-19768G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228212 | ||||||
| chr4:173228289
|
T | TCTTCTAG others(309): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0106a0001c0001t0001g0119others(3): Show | 6 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(320): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(310): Show |
47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(321): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(311): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0113a0001c0001t0001g0118others(4): Show | 7 | HG00558.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(322): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(313): Show |
1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(324): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(315): Show |
1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(326): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(321): Show |
1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(332): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(326): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0163a0001c0001t0001g0165 | 3 | HG00280.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-19676_127-1967 others(337): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(327): Show |
8 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG00741.hp1 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(338): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(327): Show |
1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(338): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(328): Show |
2 | a0001c0001t0001g0063a0004c0011t0002g0180 | 2 | HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.127-19676_127-1967 others(339): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(329): Show |
1 | a0001c0001t0001g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(340): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(330): Show |
1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(341): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(330): Show |
1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(341): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(331): Show |
1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(342): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228289
|
T | TCTTCTAG others(337): Show |
1 | a0001c0001t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(348): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | |||||
| chr4:173228503
|
A | G | 1 | a0001c0002t0001g0201 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-19477A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228503 | ||||||
| chr4:173228602
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-19378T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228602 | ||||||
| chr4:173228683
|
CA | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-19289delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228683 | |||||
| chr4:173228811
|
T | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-19169T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228811 | ||||||
| chr4:173229243
|
C | T | 16 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(13): Show | 16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-18737C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229243 | ||||||
| chr4:173229325
|
A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-18655A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229325 | ||||||
| chr4:173229361
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-18619A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229361 | ||||||
| chr4:173229711
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-18269T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229711 | ||||||
| chr4:173229748
|
T | C | 1 | a0001c0002t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-18232T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229748 | ||||||
| chr4:173229814
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(34): Show | 37 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-18166A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229814 | ||||||
| chr4:173230295
|
A | AT | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-17684dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173230295 | |||||
| chr4:173230298
|
T | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-17682T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230298 | ||||||
| chr4:173230299
|
A | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-17681A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230299 | ||||||
| chr4:173230468
|
T | C | 50 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-17512T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230468 | ||||||
| chr4:173230698
|
G | A | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-17282G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230698 | ||||||
| chr4:173230863
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-17117T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230863 | ||||||
| chr4:173231017
|
C | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0118others(2): Show | 5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-16963C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231017 | ||||||
| chr4:173231070
|
C | T | 4 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-16910C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231070 | ||||||
| chr4:173231081
|
T | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.127-16899T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231081 | ||||||
| chr4:173231158
|
C | T | 1 | a0004c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-16822C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231158 | ||||||
| chr4:173231200
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-16780T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231200 | ||||||
| chr4:173231272
|
G | A | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-16708G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231272 | ||||||
| chr4:173231512
|
G | A | 3 | a0001c0002t0009g0244a0001c0002t0009g0245a0003c0013t0001g0175 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-16468G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231512 | ||||||
| chr4:173231541
|
C | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-16439C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231541 | ||||||
| chr4:173231739
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16241A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231739 | ||||||
| chr4:173231840
|
G | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-16140G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231840 | ||||||
| chr4:173231876
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.127-16104A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231876 | ||||||
| chr4:173232041
|
A | G | 2 | a0001c0001t0001g0096a0001c0005t0003g0092 | 2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.127-15939A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232041 | ||||||
| chr4:173232215
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-15765G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232215 | ||||||
| chr4:173232230
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.127-15750G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232230 | ||||||
| chr4:173232249
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127-15731G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232249 | ||||||
| chr4:173232271
|
T | TA | 18 | a0001c0002t0001g0253a0001c0002t0001g0259a0001c0002t0001g0260others(15): Show | 18 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-15697dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173232271 | |||||
| chr4:173232611
|
T | A | 1 | a0001c0002t0011g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-15369T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232611 | ||||||
| chr4:173232636
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-15344A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232636 | ||||||
| chr4:173232810
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0142 | 2 | HG02056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.127-15170G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232810 | ||||||
| chr4:173233160
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.127-14820T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233160 | ||||||
| chr4:173233204
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(3): Show | 6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-14776G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233204 | ||||||
| chr4:173233456
|
G | A | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-14524G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233456 | ||||||
| chr4:173233597
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-14383G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233597 | ||||||
| chr4:173233999
|
G | C | 6 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0006g0170others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-13981G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233999 | ||||||
| chr4:173234019
|
G | A | 1 | a0002c0007t0007g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-13961G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234019 | ||||||
| chr4:173234077
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-13903A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234077 | ||||||
| chr4:173234221
|
G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-13759G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234221 | ||||||
| chr4:173234223
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0030others(34): Show | 37 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-13757G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234223 | ||||||
| chr4:173234367
|
T | C | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.127-13613T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234367 | ||||||
| chr4:173234503
|
G | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.127-13477G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234503 | ||||||
| chr4:173234515
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-13465A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234515 | ||||||
| chr4:173234590
|
A | T | 1 | a0001c0002t0001g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127-13390A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234590 | ||||||
| chr4:173234756
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.127-13224A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234756 | ||||||
| chr4:173234842
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-13138C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234842 | ||||||
| chr4:173234909
|
C | T | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.127-13071C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234909 | ||||||
| chr4:173234994
|
A | G | 4 | a0001c0004t0001g0076a0001c0004t0001g0077a0001c0004t0001g0084others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-12986A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234994 | ||||||
| chr4:173235219
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.127-12761A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235219 | ||||||
| chr4:173235232
|
C | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-12748C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235232 | ||||||
| chr4:173235313
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12667C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235313 | ||||||
| chr4:173235387
|
A | G | 64 | a0001c0001t0001g0142a0001c0002t0001g0016a0001c0002t0001g0017others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.127-12593A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235387 | ||||||
| chr4:173235556
|
C | CT | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.127-12410dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173235556 | |||||
| chr4:173235556
|
C | CTTT | 9 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0259others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-12412_127-1241 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173235556 | |||||
| chr4:173235644
|
C | T | 2 | a0001c0004t0001g0076a0001c0004t0001g0077 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-12336C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235644 | ||||||
| chr4:173235694
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.127-12286T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235694 | ||||||
| chr4:173235855
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-12125C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235855 | ||||||
| chr4:173235890
|
A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-12090A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235890 | ||||||
| chr4:173236025
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01257.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.127-11955G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236025 | ||||||
| chr4:173236060
|
G | A | 35 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(32): Show | 35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-11920G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236060 | ||||||
| chr4:173236140
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-11840A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236140 | ||||||
| chr4:173236311
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0151 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.127-11669A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236311 | ||||||
| chr4:173236468
|
A | G | 15 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-11512A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236468 | ||||||
| chr4:173236538
|
C | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(26): Show | 29 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-11442C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236538 | ||||||
| chr4:173236909
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0102others(2): Show | 5 | HG02257.hp2 HG02572.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-11071A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236909 | ||||||
| chr4:173236929
|
A | G | 2 | a0001c0004t0001g0076a0001c0004t0001g0077 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-11051A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236929 | ||||||
| chr4:173236940
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-11040T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236940 | ||||||
| chr4:173236980
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-11000G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236980 | ||||||
| chr4:173236981
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.127-10999A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236981 | ||||||
| chr4:173237012
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-10968G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237012 | ||||||
| chr4:173237025
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.127-10955T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237025 | ||||||
| chr4:173237308
|
A | G | 5 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10672A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237308 | ||||||
| chr4:173237340
|
G | T | 2 | a0001c0003t0002g0169a0001c0003t0002g0257 | 2 | HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127-10640G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237340 | ||||||
| chr4:173237561
|
T | C | 1 | a0001c0002t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.127-10419T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237561 | ||||||
| chr4:173237759
|
TA | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.127-10206delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173237759 | |||||
| chr4:173237849
|
G | A | 3 | a0001c0002t0001g0207a0001c0002t0001g0216a0001c0002t0001g0221 | 3 | HG01255.hp2 HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.127-10131G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237849 | ||||||
| chr4:173238115
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-9865A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238115 | ||||||
| chr4:173238124
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-9856A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238124 | ||||||
| chr4:173238216
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-9764T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238216 | ||||||
| chr4:173238300
|
T | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-9680T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238300 | ||||||
| chr4:173238318
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-9662G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238318 | ||||||
| chr4:173238637
|
G | A | 63 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-9343G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238637 | ||||||
| chr4:173238768
|
A | G | 8 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-9212A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238768 | ||||||
| chr4:173239210
|
G | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-8770G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239210 | ||||||
| chr4:173239211
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(8): Show | 11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-8769T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239211 | ||||||
| chr4:173239524
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-8456C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239524 | ||||||
| chr4:173239525
|
G | A | 7 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0078others(4): Show | 7 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-8455G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239525 | ||||||
| chr4:173239579
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(21): Show | 24 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.127-8401A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239579 | ||||||
| chr4:173239694
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-8286C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239694 | ||||||
| chr4:173240137
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-7843A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240137 | ||||||
| chr4:173240357
|
A | AT | 18 | a0001c0002t0001g0200a0001c0002t0001g0215a0001c0002t0001g0253others(15): Show | 18 | HG01192.hp2 HG01346.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-7594dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
AT | A | 22 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0003g0080others(19): Show | 22 | HG01081.hp2 HG02027.hp2 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-7594delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATT | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-7595_127-7594d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATTT | A | 8 | a0001c0001t0001g0266a0001c0001t0005g0072a0001c0001t0005g0085others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-7596_127-7594d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATTTT | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0002g0035others(4): Show | 7 | HG02055.hp2 HG02738.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-7597_127-7594d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATTTTT | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 59 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.127-7598_127-7594d others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATTTTTT | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.127-7599_127-7594d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240357
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0002t0001g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-7609_127-7594d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | |||||
| chr4:173240658
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-7322C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240658 | ||||||
| chr4:173240748
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7232T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240748 | ||||||
| chr4:173241110
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-6870C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241110 | ||||||
| chr4:173241137
|
G | A | 2 | a0001c0002t0006g0170a0001c0002t0006g0171 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.127-6843G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241137 | ||||||
| chr4:173241167
|
T | C | 2 | a0001c0002t0001g0259a0001c0002t0002g0182 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-6813T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241167 | ||||||
| chr4:173241223
|
A | AAAAG | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.127-6755_127-6754i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | |||||
| chr4:173241223
|
A | AAAG | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(41): Show | 44 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-6754_127-6752d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | |||||
| chr4:173241223
|
A | AAG | 7 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0079others(4): Show | 7 | HG01257.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-6756_127-6755i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | |||||
| chr4:173241316
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-6664G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241316 | ||||||
| chr4:173241589
|
G | A | 4 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0194others(1): Show | 4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6391G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241589 | ||||||
| chr4:173241934
|
T | G | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-6046T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241934 | ||||||
| chr4:173242018
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.127-5962T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242018 | ||||||
| chr4:173242031
|
T | C | 17 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-5949T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242031 | ||||||
| chr4:173242209
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-5771A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242209 | ||||||
| chr4:173242247
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.127-5733G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242247 | ||||||
| chr4:173242446
|
T | C | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-5534T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242446 | ||||||
| chr4:173242550
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-5430G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242550 | ||||||
| chr4:173242861
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-5119T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242861 | ||||||
| chr4:173243006
|
A | C | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-4974A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243006 | ||||||
| chr4:173243221
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0100others(3): Show | 6 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-4759T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243221 | ||||||
| chr4:173243569
|
G | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-4411G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243569 | ||||||
| chr4:173243715
|
A | C | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-4265A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243715 | ||||||
| chr4:173243784
|
T | C | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-4196T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243784 | ||||||
| chr4:173243820
|
G | T | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.127-4160G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243820 | ||||||
| chr4:173243879
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-4101A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243879 | ||||||
| chr4:173243975
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.127-4005C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243975 | ||||||
| chr4:173244163
|
G | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 7 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-3817G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244163 | ||||||
| chr4:173244234
|
C | G | 10 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(7): Show | 10 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-3746C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244234 | ||||||
| chr4:173244328
|
C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-3652C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244328 | ||||||
| chr4:173244391
|
A | G | 1 | a0001c0002t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.127-3589A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244391 | ||||||
| chr4:173244397
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127-3583A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244397 | ||||||
| chr4:173244984
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-2996G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244984 | ||||||
| chr4:173245197
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-2783G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245197 | ||||||
| chr4:173245215
|
CA | C | 30 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0096others(27): Show | 30 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-2747delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | |||||
| chr4:173245215
|
CAA | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.127-2748_127-2747d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | |||||
| chr4:173245215
|
CAAA | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0064others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.127-2749_127-2747d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | |||||
| chr4:173245374
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-2606T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245374 | ||||||
| chr4:173245395
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-2585T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245395 | ||||||
| chr4:173245399
|
A | G | 1 | a0007c0010t0003g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-2581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245399 | ||||||
| chr4:173245739
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.127-2241C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245739 | ||||||
| chr4:173245795
|
G | C | 10 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(7): Show | 10 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-2185G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245795 | ||||||
| chr4:173245823
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127-2157A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245823 | ||||||
| chr4:173245841
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.127-2139C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245841 | ||||||
| chr4:173246095
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.127-1885A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246095 | ||||||
| chr4:173246143
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-1837C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246143 | ||||||
| chr4:173246269
|
C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.127-1711C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246269 | ||||||
| chr4:173246830
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0118others(2): Show | 5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1150A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246830 | ||||||
| chr4:173246861
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0153 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-1119T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246861 | ||||||
| chr4:173246936
|
G | A | 6 | a0001c0001t0001g0090a0001c0002t0006g0170a0001c0002t0006g0171others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1044G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246936 | ||||||
| chr4:173246968
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-1012C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246968 | ||||||
| chr4:173246983
|
T | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-997T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246983 | ||||||
| chr4:173247268
|
G | C | 2 | a0001c0002t0009g0244a0001c0002t0009g0245 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-712G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247268 | ||||||
| chr4:173247295
|
C | T | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-685C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247295 | ||||||
| chr4:173247300
|
T | C | 1 | a0001c0002t0009g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.127-680T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247300 | ||||||
| chr4:173247416
|
G | C | 1 | a0001c0005t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127-564G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247416 | ||||||
| chr4:173247474
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-506G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247474 | ||||||
| chr4:173247480
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.127-500T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247480 | ||||||
| chr4:173247588
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.127-392C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247588 | ||||||
| chr4:173247692
|
T | G | 1 | a0001c0002t0001g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-288T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247692 | ||||||
| chr4:173248895
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(23): Show | 26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+455G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173248895 | ||||||
| chr4:173248940
|
TC | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.587+503delC | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173248940 | |||||
| chr4:173249509
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.587+1069A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249509 | ||||||
| chr4:173249584
|
A | C | 1 | a0001c0002t0009g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.587+1144A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249584 | ||||||
| chr4:173249644
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+1204G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249644 | ||||||
| chr4:173250001
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.587+1561A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250001 | ||||||
| chr4:173250231
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+1791G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250231 | ||||||
| chr4:173250458
|
A | G | 3 | a0001c0001t0001g0094a0001c0005t0001g0099a0001c0005t0003g0098 | 3 | HG02723.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.587+2018A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250458 | ||||||
| chr4:173250460
|
C | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0100others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+2020C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250460 | ||||||
| chr4:173250482
|
T | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 26 | HG01192.hp1 HG01884.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+2042T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250482 | ||||||
| chr4:173250487
|
C | T | 1 | a0007c0010t0003g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.587+2047C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250487 | ||||||
| chr4:173250488
|
T | C | 1 | a0001c0002t0002g0192 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.587+2048T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250488 | ||||||
| chr4:173250530
|
T | C | 11 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0004t0001g0006others(8): Show | 11 | HG01346.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.587+2090T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250530 | ||||||
| chr4:173250620
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.587+2180C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250620 | ||||||
| chr4:173250767
|
C | T | 3 | a0001c0001t0001g0090a0002c0007t0007g0177a0002c0007t0007g0178 | 3 | HG03130.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587+2327C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250767 | ||||||
| chr4:173250997
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.587+2557C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250997 | ||||||
| chr4:173251003
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+2563G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251003 | ||||||
| chr4:173251149
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+2709T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251149 | ||||||
| chr4:173251208
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(22): Show | 25 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.587+2768C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251208 | ||||||
| chr4:173251613
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.587+3173G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251613 | ||||||
| chr4:173251732
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+3292G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251732 | ||||||
| chr4:173251994
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.587+3554T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251994 | ||||||
| chr4:173252100
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+3660A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252100 | ||||||
| chr4:173252150
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.587+3710T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252150 | ||||||
| chr4:173252592
|
G | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(89): Show |
intron_variant | MODIFIER | c.587+4152G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252592 | ||||||
| chr4:173252635
|
C | T | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+4195C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252635 | ||||||
| chr4:173252809
|
A | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.587+4369A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252809 | ||||||
| chr4:173253042
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+4602A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253042 | ||||||
| chr4:173253150
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0014g0057 | 2 | HG01346.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.587+4710C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253150 | ||||||
| chr4:173253325
|
C | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+4885C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253325 | ||||||
| chr4:173253338
|
T | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+4898T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253338 | ||||||
| chr4:173253504
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587+5064G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253504 | ||||||
| chr4:173253538
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.587+5098T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253538 | ||||||
| chr4:173253566
|
A | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5126A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253566 | ||||||
| chr4:173253818
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.587+5378G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253818 | ||||||
| chr4:173253837
|
T | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5397T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253837 | ||||||
| chr4:173253852
|
G | C | 2 | a0001c0003t0002g0169a0001c0003t0002g0257 | 2 | HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.587+5412G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253852 | ||||||
| chr4:173254001
|
T | G | 1 | a0001c0002t0001g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.587+5561T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254001 | ||||||
| chr4:173254089
|
T | C | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+5649T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254089 | ||||||
| chr4:173254216
|
A | T | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+5776A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254216 | ||||||
| chr4:173254364
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.587+5924A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254364 | ||||||
| chr4:173254374
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5934T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254374 | ||||||
| chr4:173254653
|
A | C | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+6213A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254653 | ||||||
| chr4:173254655
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.587+6215A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254655 | ||||||
| chr4:173254754
|
G | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.587+6314G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254754 | ||||||
| chr4:173254764
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587+6324T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254764 | ||||||
| chr4:173254932
|
T | C | 5 | a0001c0002t0002g0020a0001c0002t0002g0240a0001c0002t0002g0241others(2): Show | 5 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+6492T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254932 | ||||||
| chr4:173254944
|
T | G | 3 | a0001c0002t0001g0200a0001c0002t0001g0235a0001c0002t0013g0233 | 3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.587+6504T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254944 | ||||||
| chr4:173255085
|
C | T | 1 | a0005c0009t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.587+6645C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255085 | ||||||
| chr4:173255158
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 44 | HG00621.hp1 HG01257.hp1 HG01993.hp2 others(41): Show |
intron_variant | MODIFIER | c.587+6718A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255158 | ||||||
| chr4:173255177
|
A | C | 5 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+6737A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255177 | ||||||
| chr4:173255279
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+6839G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255279 | ||||||
| chr4:173255455
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+7015G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255455 | ||||||
| chr4:173255542
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+7102G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255542 | ||||||
| chr4:173255563
|
A | G | 1 | a0001c0003t0002g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.587+7123A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255563 | ||||||
| chr4:173255743
|
G | A | 1 | a0001c0002t0003g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.587+7303G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255743 | ||||||
| chr4:173255828
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+7388G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255828 | ||||||
| chr4:173255836
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.587+7396C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255836 | ||||||
| chr4:173256207
|
A | G | 5 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(2): Show | 5 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+7767A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256207 | ||||||
| chr4:173256270
|
A | C | 1 | a0001c0001t0002g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.587+7830A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256270 | ||||||
| chr4:173256329
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+7889G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256329 | ||||||
| chr4:173256494
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.587+8054G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256494 | ||||||
| chr4:173256502
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.587+8062A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256502 | ||||||
| chr4:173256692
|
T | C | 1 | a0001c0002t0001g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.587+8252T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256692 | ||||||
| chr4:173256821
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.587+8381A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256821 | ||||||
| chr4:173256926
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.587+8486T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256926 | ||||||
| chr4:173257058
|
C | T | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+8618C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257058 | ||||||
| chr4:173257059
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+8619A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257059 | ||||||
| chr4:173257102
|
C | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+8662C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257102 | ||||||
| chr4:173257163
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00621.hp1 HG01257.hp1 HG01993.hp2 others(45): Show |
intron_variant | MODIFIER | c.587+8723T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257163 | ||||||
| chr4:173257211
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+8771A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257211 | ||||||
| chr4:173257777
|
C | T | 2 | a0001c0002t0001g0216a0001c0002t0001g0221 | 2 | HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.587+9337C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257777 | ||||||
| chr4:173257808
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+9368T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257808 | ||||||
| chr4:173257884
|
G | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(30): Show | 33 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.587+9444G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257884 | ||||||
| chr4:173257906
|
G | A | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587+9466G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257906 | ||||||
| chr4:173258031
|
T | G | 1 | a0001c0002t0001g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587+9591T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258031 | ||||||
| chr4:173258053
|
AAGG | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+9618_587+9620d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173258053 | |||||
| chr4:173258342
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(28): Show | 31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+9902T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258342 | ||||||
| chr4:173258350
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.587+9910C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258350 | ||||||
| chr4:173258523
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 80 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.587+10083T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258523 | ||||||
| chr4:173258560
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+10120C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258560 | ||||||
| chr4:173258581
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587+10141C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258581 | ||||||
| chr4:173258637
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+10197C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258637 | ||||||
| chr4:173258686
|
A | G | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+10246A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258686 | ||||||
| chr4:173258936
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587+10496C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258936 | ||||||
| chr4:173258987
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+10547G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258987 | ||||||
| chr4:173259171
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.587+10731A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259171 | ||||||
| chr4:173259188
|
C | T | 1 | a0001c0002t0006g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.587+10748C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259188 | ||||||
| chr4:173259410
|
C | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(29): Show | 32 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.587+10970C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259410 | ||||||
| chr4:173259428
|
C | CT | 16 | a0001c0003t0002g0021a0001c0003t0002g0176a0001c0003t0002g0181others(13): Show | 16 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+11001dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173259428 | |||||
| chr4:173259474
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+11034C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259474 | ||||||
| chr4:173259485
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(24): Show | 27 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.587+11045A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259485 | ||||||
| chr4:173259677
|
G | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+11237G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259677 | ||||||
| chr4:173259700
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587+11260C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259700 | ||||||
| chr4:173259933
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.587+11493C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259933 | ||||||
| chr4:173260054
|
GTA | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0004g0112 | 3 | HG02056.hp1 NA18945.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.587+11617_587+1161 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173260054 | |||||
| chr4:173260239
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(28): Show | 31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+11799T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260239 | ||||||
| chr4:173260245
|
A | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+11805A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260245 | ||||||
| chr4:173260374
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.587+11934G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260374 | ||||||
| chr4:173260458
|
G | A | 1 | a0004c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.587+12018G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260458 | ||||||
| chr4:173260503
|
T | TA | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+12064dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173260503 | |||||
| chr4:173260513
|
G | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12073G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260513 | ||||||
| chr4:173260581
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12141G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260581 | ||||||
| chr4:173260764
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+12324A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260764 | ||||||
| chr4:173260765
|
C | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.587+12325C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260765 | ||||||
| chr4:173260799
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12359T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260799 | ||||||
| chr4:173260933
|
C | T | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+12493C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260933 | ||||||
| chr4:173261028
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.587+12588C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261028 | ||||||
| chr4:173261232
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+12792G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261232 | ||||||
| chr4:173261304
|
C | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12864C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261304 | ||||||
| chr4:173261390
|
G | GT | 23 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(20): Show | 23 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.587+12961dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173261390 | |||||
| chr4:173261426
|
G | C | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+12986G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261426 | ||||||
| chr4:173261459
|
A | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+13019A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261459 | ||||||
| chr4:173261481
|
G | A | 21 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(18): Show | 21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.587+13041G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261481 | ||||||
| chr4:173261502
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(28): Show | 31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+13062A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261502 | ||||||
| chr4:173261518
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+13078A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261518 | ||||||
| chr4:173261614
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+13174C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261614 | ||||||
| chr4:173261696
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587+13256G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261696 | ||||||
| chr4:173261743
|
C | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+13303C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261743 | ||||||
| chr4:173262129
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+13689A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262129 | ||||||
| chr4:173262167
|
A | T | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587+13727A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262167 | ||||||
| chr4:173262305
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+13865C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262305 | ||||||
| chr4:173262441
|
A | T | 2 | a0001c0002t0001g0188a0001c0002t0002g0192 | 2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.587+14001A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262441 | ||||||
| chr4:173262613
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587+14173T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262613 | ||||||
| chr4:173262680
|
G | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+14240G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262680 | ||||||
| chr4:173262744
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+14304C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262744 | ||||||
| chr4:173262753
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(23): Show | 26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+14313T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262753 | ||||||
| chr4:173262760
|
ACCCAT | A | 21 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(18): Show | 21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.587+14322_587+1432 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173262760 | |||||
| chr4:173262799
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.587+14359A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262799 | ||||||
| chr4:173263113
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 66 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.587+14673C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263113 | ||||||
| chr4:173263195
|
GA | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.587+14760delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173263195 | |||||
| chr4:173263268
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.587+14828G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263268 | ||||||
| chr4:173263552
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.587+15112A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263552 | ||||||
| chr4:173263697
|
A | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+15257A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263697 | ||||||
| chr4:173263698
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+15258A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263698 | ||||||
| chr4:173263864
|
C | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+15424C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263864 | ||||||
| chr4:173264036
|
A | G | 1 | a0001c0002t0001g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.587+15596A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264036 | ||||||
| chr4:173264070
|
G | A | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+15630G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264070 | ||||||
| chr4:173264169
|
A | G | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+15729A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264169 | ||||||
| chr4:173264199
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.587+15759G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264199 | ||||||
| chr4:173264435
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(30): Show | 33 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.587+15995G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264435 | ||||||
| chr4:173264692
|
T | C | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+16252T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264692 | ||||||
| chr4:173264732
|
C | T | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.587+16292C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264732 | ||||||
| chr4:173264749
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.587+16309A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264749 | ||||||
| chr4:173264878
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+16438G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264878 | ||||||
| chr4:173264893
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+16453C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264893 | ||||||
| chr4:173264913
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.587+16473G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264913 | ||||||
| chr4:173264957
|
A | G | 3 | a0001c0002t0001g0203a0001c0002t0001g0217a0001c0002t0001g0228 | 3 | HG03704.hp2 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.587+16517A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264957 | ||||||
| chr4:173264976
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0161 | 3 | NA18975.hp2 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.587+16536A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264976 | ||||||
| chr4:173265101
|
G | A | 2 | a0001c0003t0002g0021a0001c0003t0002g0250 | 2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.587+16661G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265101 | ||||||
| chr4:173265118
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.587+16678C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265118 | ||||||
| chr4:173265171
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.587+16731G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265171 | ||||||
| chr4:173265175
|
G | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+16735G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265175 | ||||||
| chr4:173265220
|
T | C | 1 | a0001c0002t0001g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.587+16780T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265220 | ||||||
| chr4:173265493
|
C | A | 2 | a0001c0002t0006g0170a0001c0002t0006g0171 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.587+17053C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265493 | ||||||
| chr4:173265568
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.587+17128C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265568 | ||||||
| chr4:173265587
|
A | ATC | 7 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG00738.hp2 HG01256.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+17179_587+1718 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
A | ATCTC | 14 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0064others(11): Show | 14 | HG01257.hp1 HG01891.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.587+17177_587+1718 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
A | ATCTCTC | 6 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0069others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.587+17175_587+1718 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
A | ATCTCTCT others(1): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0079others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+17173_587+1718 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
A | ATCTCTCT others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.587+17171_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
ATC | A | 6 | a0001c0001t0001g0266a0001c0002t0001g0184a0001c0002t0001g0230others(3): Show | 6 | HG02273.hp1 HG02280.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.587+17179_587+1718 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
ATCTC | A | 61 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0061others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.587+17177_587+1718 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
ATCTCTCT others(1): Show |
A | 14 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+17173_587+1718 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265587
|
ATCTCTCT others(3): Show |
A | 12 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0002t0006g0170others(9): Show | 12 | HG01346.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+17171_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | |||||
| chr4:173265611
|
CTCTCTCT others(3): Show |
C | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+17177_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265611 | |||||
| chr4:173265621
|
G | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17181G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265621 | ||||||
| chr4:173266039
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17599C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266039 | ||||||
| chr4:173266079
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17639G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266079 | ||||||
| chr4:173266255
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.587+17815G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266255 | ||||||
| chr4:173266256
|
T | G | 3 | a0001c0001t0005g0072a0001c0002t0009g0244a0001c0002t0009g0245 | 3 | HG02257.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.587+17816T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266256 | ||||||
| chr4:173266282
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 27 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.587+17842A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266282 | ||||||
| chr4:173266325
|
G | C | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587+17885G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266325 | ||||||
| chr4:173266337
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(7): Show | 10 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+17897A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266337 | ||||||
| chr4:173266432
|
T | C | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+17992T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266432 | ||||||
| chr4:173266486
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+18046A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266486 | ||||||
| chr4:173266866
|
AG | A | 4 | a0001c0001t0001g0103a0001c0001t0002g0042a0001c0002t0001g0017others(1): Show | 4 | HG00621.hp1 HG01934.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+18429delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266866 | |||||
| chr4:173266867
|
GGGTGTGT others(10): Show |
G | 1 | a0001c0001t0001g0059 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.587+18429_587+1844 others(21): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266867 | |||||
| chr4:173266868
|
G | GGT | 38 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0045others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.587+18486_587+1848 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
G | GGTGT | 21 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG00423.hp1 HG00558.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.587+18484_587+1848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
G | GGTGTGT | 3 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0002t0001g0222 | 3 | HG01109.hp2 NA18942.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.587+18482_587+1848 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0069a0001c0001t0001g0137a0001c0001t0002g0040others(5): Show | 8 | HG02040.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+18480_587+1848 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
G | GGTGTGTG others(3): Show |
1 | a0001c0004t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.587+18478_587+1848 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
G | GT | 5 | a0001c0001t0001g0001a0001c0001t0002g0029a0001c0003t0002g0247others(2): Show | 5 | HG01993.hp2 HG02615.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+18428_587+1842 others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | ||||||
| chr4:173266868
|
G | GTGTGTGT others(4): Show |
1 | a0001c0003t0012g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.587+18428_587+1842 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | ||||||
| chr4:173266868
|
G | T | 1 | a0001c0001t0001g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.587+18428G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | ||||||
| chr4:173266868
|
GGT | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0052a0001c0001t0001g0061others(46): Show | 49 | HG00323.hp2 HG01070.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.587+18486_587+1848 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGT | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0091others(17): Show | 20 | HG00280.hp1 HG01255.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.587+18484_587+1848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGT | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0094a0001c0001t0001g0111others(4): Show | 7 | HG00558.hp2 HG00621.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+18482_587+1848 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0113a0001c0002t0001g0186a0001c0002t0001g0220others(4): Show | 7 | HG01243.hp2 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+18480_587+1848 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(3): Show |
G | 11 | a0001c0001t0001g0266a0001c0002t0001g0194a0001c0002t0001g0195others(8): Show | 11 | HG00323.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587+18478_587+1848 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0041a0001c0002t0002g0020a0001c0002t0002g0241others(2): Show | 5 | HG01943.hp1 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+18476_587+1848 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(7): Show |
G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.587+18474_587+1848 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(9): Show |
G | 3 | a0001c0002t0001g0016a0001c0002t0001g0225a0001c0005t0003g0092 | 3 | HG01978.hp1 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.587+18472_587+1848 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(11): Show |
G | 4 | a0001c0001t0001g0128a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG00140.hp1 HG02056.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+18470_587+1848 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(13): Show |
G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(6): Show | 9 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+18468_587+1848 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266868
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.587+18466_587+1848 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | |||||
| chr4:173266870
|
T | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+18430T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266870 | ||||||
| chr4:173266874
|
T | G | 2 | a0001c0001t0001g0049a0001c0002t0001g0262 | 2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.587+18434T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266874 | ||||||
| chr4:173266893
|
G | A | 1 | a0001c0002t0003g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.587+18453G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266893 | ||||||
| chr4:173266939
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.587+18499T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266939 | ||||||
| chr4:173266969
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.587+18529A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266969 | ||||||
| chr4:173267063
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+18623G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267063 | ||||||
| chr4:173267123
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+18683T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267123 | ||||||
| chr4:173267128
|
A | G | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+18688A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267128 | ||||||
| chr4:173267648
|
G | C | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+19208G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267648 | ||||||
| chr4:173267763
|
T | C | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.587+19323T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267763 | ||||||
| chr4:173267773
|
TA | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(23): Show | 26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+19335delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173267773 | |||||
| chr4:173268204
|
C | CA | 7 | a0001c0001t0001g0136a0001c0002t0001g0204a0001c0002t0001g0205others(4): Show | 7 | HG01070.hp2 HG01257.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+19769dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268204 | |||||
| chr4:173268209
|
A | C | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+19769A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268209 | ||||||
| chr4:173268298
|
A | T | 1 | a0001c0002t0002g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.587+19858A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268298 | ||||||
| chr4:173268328
|
C | T | 1 | a0001c0002t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+19888C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268328 | ||||||
| chr4:173268355
|
G | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+19915G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268355 | ||||||
| chr4:173268441
|
T | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0118others(2): Show | 5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+20001T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268441 | ||||||
| chr4:173268530
|
G | GT | 76 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0041others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.587+20117dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | |||||
| chr4:173268530
|
G | GTT | 76 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.587+20116_587+2011 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | |||||
| chr4:173268530
|
G | GTTT | 26 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(23): Show | 26 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.587+20115_587+2011 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | |||||
| chr4:173268530
|
GT | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0082others(5): Show | 8 | HG01257.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+20117delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | |||||
| chr4:173268530
|
GTTTT | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(26): Show | 29 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.587+20114_587+2011 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | |||||
| chr4:173268655
|
C | T | 4 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0194others(1): Show | 4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+20215C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268655 | ||||||
| chr4:173268697
|
AT | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(26): Show | 29 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.587+20272delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268697 | |||||
| chr4:173268713
|
G | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+20273G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268713 | ||||||
| chr4:173268715
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.587+20275A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268715 | ||||||
| chr4:173268760
|
C | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+20320C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268760 | ||||||
| chr4:173268781
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+20341C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268781 | ||||||
| chr4:173268958
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+20518T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268958 | ||||||
| chr4:173269071
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0041others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.587+20631G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269071 | ||||||
| chr4:173269077
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+20637A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269077 | ||||||
| chr4:173269097
|
G | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+20657G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269097 | ||||||
| chr4:173269159
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(32): Show | 35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.587+20719C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269159 | ||||||
| chr4:173269302
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+20862A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269302 | ||||||
| chr4:173269482
|
G | T | 1 | a0001c0002t0001g0225 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.587+21042G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269482 | ||||||
| chr4:173269630
|
A | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.587+21190A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269630 | ||||||
| chr4:173269800
|
T | C | 1 | a0001c0003t0002g0257 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.587+21360T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269800 | ||||||
| chr4:173269980
|
G | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+21540G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269980 | ||||||
| chr4:173270013
|
G | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+21573G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270013 | ||||||
| chr4:173270110
|
G | A | 1 | a0001c0002t0001g0226 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.587+21670G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270110 | ||||||
| chr4:173270116
|
C | A | 5 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+21676C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270116 | ||||||
| chr4:173270127
|
T | C | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+21687T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270127 | ||||||
| chr4:173270294
|
G | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(32): Show | 35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.588-21814G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270294 | ||||||
| chr4:173270462
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-21646T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270462 | ||||||
| chr4:173270544
|
G | A | 7 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(4): Show | 7 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-21564G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270544 | ||||||
| chr4:173270681
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588-21427G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270681 | ||||||
| chr4:173270749
|
A | G | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-21359A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270749 | ||||||
| chr4:173270806
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.588-21302C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270806 | ||||||
| chr4:173271386
|
C | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0151 | 2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.588-20722C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173271386 | ||||||
| chr4:173271435
|
CTGTT | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 46 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-20659_588-2065 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173271435 | |||||
| chr4:173271453
|
A | G | 8 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(5): Show | 8 | HG01081.hp2 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-20655A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173271453 | ||||||
| chr4:173272464
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-19644G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272464 | ||||||
| chr4:173272642
|
G | A | 1 | a0007c0010t0003g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.588-19466G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272642 | ||||||
| chr4:173272927
|
C | G | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-19181C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272927 | ||||||
| chr4:173272947
|
C | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.588-19161C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272947 | ||||||
| chr4:173273018
|
C | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0100others(3): Show | 6 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-19090C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273018 | ||||||
| chr4:173273170
|
T | C | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-18938T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273170 | ||||||
| chr4:173273302
|
C | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.588-18806C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273302 | ||||||
| chr4:173273369
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.588-18739T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273369 | ||||||
| chr4:173273384
|
A | G | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-18724A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273384 | ||||||
| chr4:173273419
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.588-18689A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273419 | ||||||
| chr4:173273523
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588-18585C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273523 | ||||||
| chr4:173273578
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.588-18530C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273578 | ||||||
| chr4:173273658
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-18450G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273658 | ||||||
| chr4:173273660
|
A | T | 2 | a0001c0001t0001g0146a0001c0002t0001g0215 | 2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.588-18448A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273660 | ||||||
| chr4:173273788
|
C | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 46 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-18320C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273788 | ||||||
| chr4:173273805
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-18303T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273805 | ||||||
| chr4:173274807
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588-17301C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274807 | ||||||
| chr4:173274822
|
C | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG02451.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588-17286C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274822 | ||||||
| chr4:173274890
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.588-17218G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274890 | ||||||
| chr4:173274934
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-17174T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274934 | ||||||
| chr4:173274983
|
C | T | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.588-17125C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274983 | ||||||
| chr4:173275117
|
T | G | 5 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.588-16991T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275117 | ||||||
| chr4:173275273
|
G | C | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-16835G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275273 | ||||||
| chr4:173275335
|
G | T | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-16773G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275335 | ||||||
| chr4:173275445
|
T | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-16663T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275445 | ||||||
| chr4:173275626
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(9): Show | 12 | HG01257.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-16482C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275626 | ||||||
| chr4:173275681
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.588-16427C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275681 | ||||||
| chr4:173275694
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.588-16414A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275694 | ||||||
| chr4:173275699
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-16409T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275699 | ||||||
| chr4:173275762
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-16346G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275762 | ||||||
| chr4:173275917
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-16191C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275917 | ||||||
| chr4:173275930
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.588-16178C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275930 | ||||||
| chr4:173276127
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(23): Show | 26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.588-15981A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276127 | ||||||
| chr4:173276363
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.588-15745A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276363 | ||||||
| chr4:173276606
|
G | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-15502G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276606 | ||||||
| chr4:173276699
|
G | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(30): Show | 33 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.588-15409G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276699 | ||||||
| chr4:173276731
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.588-15377C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276731 | ||||||
| chr4:173276815
|
AT | A | 6 | a0001c0002t0002g0020a0001c0002t0002g0192a0001c0002t0002g0240others(3): Show | 6 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-15283delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173276815 | |||||
| chr4:173276916
|
A | C | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-15192A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276916 | ||||||
| chr4:173277044
|
A | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(37): Show | 40 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.588-15064A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277044 | ||||||
| chr4:173277192
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.588-14916T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277192 | ||||||
| chr4:173277418
|
C | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(23): Show | 26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.588-14690C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277418 | ||||||
| chr4:173277763
|
G | T | 1 | a0001c0002t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-14345G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277763 | ||||||
| chr4:173277996
|
AGAG | A | 21 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(18): Show | 21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.588-14108_588-1410 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173277996 | |||||
| chr4:173278215
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588-13893T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278215 | ||||||
| chr4:173278320
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.588-13788T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278320 | ||||||
| chr4:173278339
|
A | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-13769A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278339 | ||||||
| chr4:173278560
|
A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-13548A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278560 | ||||||
| chr4:173278705
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.588-13403C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278705 | ||||||
| chr4:173278788
|
A | C | 3 | a0001c0002t0001g0207a0001c0002t0001g0216a0001c0002t0001g0221 | 3 | HG01255.hp2 HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.588-13320A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278788 | ||||||
| chr4:173278846
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.588-13262C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278846 | ||||||
| chr4:173278893
|
C | A | 1 | a0001c0008t0002g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.588-13215C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278893 | ||||||
| chr4:173278982
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(32): Show | 35 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.588-13126C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278982 | ||||||
| chr4:173279121
|
A | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-12987A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279121 | ||||||
| chr4:173279345
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.588-12763G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279345 | ||||||
| chr4:173279435
|
C | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-12673C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279435 | ||||||
| chr4:173279771
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.588-12337G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279771 | ||||||
| chr4:173279783
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0032others(66): Show | 69 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.588-12325A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279783 | ||||||
| chr4:173279990
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-12118A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279990 | ||||||
| chr4:173280095
|
C | A | 1 | a0001c0001t0010g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.588-12013C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280095 | ||||||
| chr4:173280106
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-11999dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173280106 | |||||
| chr4:173280277
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.588-11831G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280277 | ||||||
| chr4:173280340
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(24): Show | 27 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.588-11768A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280340 | ||||||
| chr4:173280420
|
A | ATT | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-11683_588-1168 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173280420 | |||||
| chr4:173280815
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-11293C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280815 | ||||||
| chr4:173280947
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.588-11161C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280947 | ||||||
| chr4:173281085
|
C | T | 9 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0005t0001g0099others(6): Show | 9 | HG01346.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-11023C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281085 | ||||||
| chr4:173281162
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-10946G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281162 | ||||||
| chr4:173281186
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-10922C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281186 | ||||||
| chr4:173281346
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588-10762G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281346 | ||||||
| chr4:173281351
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0032others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.588-10757A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281351 | ||||||
| chr4:173281438
|
A | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-10670A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281438 | ||||||
| chr4:173281768
|
C | T | 1 | a0005c0009t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.588-10340C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281768 | ||||||
| chr4:173281779
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-10329C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281779 | ||||||
| chr4:173282010
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-10098T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282010 | ||||||
| chr4:173282134
|
A | G | 20 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(17): Show | 20 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.588-9974A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282134 | ||||||
| chr4:173282218
|
T | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.588-9890T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282218 | ||||||
| chr4:173282373
|
G | C | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-9735G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282373 | ||||||
| chr4:173282391
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0039others(28): Show | 31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.588-9717A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282391 | ||||||
| chr4:173282449
|
T | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-9659T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282449 | ||||||
| chr4:173282471
|
G | GT | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.588-9636dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173282471 | |||||
| chr4:173282608
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.588-9500G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282608 | ||||||
| chr4:173282646
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-9462G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282646 | ||||||
| chr4:173282720
|
A | G | 21 | a0001c0002t0001g0207a0001c0002t0001g0216a0001c0002t0001g0221others(18): Show | 21 | HG01074.hp2 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.588-9388A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282720 | ||||||
| chr4:173283006
|
T | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(39): Show | 42 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.588-9102T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283006 | ||||||
| chr4:173283329
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-8779A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283329 | ||||||
| chr4:173283377
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.588-8731T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283377 | ||||||
| chr4:173283500
|
C | T | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-8608C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283500 | ||||||
| chr4:173283524
|
C | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(33): Show | 36 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.588-8584C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283524 | ||||||
| chr4:173283548
|
G | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-8560G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283548 | ||||||
| chr4:173283635
|
G | C | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.588-8473G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283635 | ||||||
| chr4:173283635
|
G | GA | 11 | a0001c0001t0001g0070a0001c0001t0001g0140a0001c0001t0001g0152others(8): Show | 11 | HG02027.hp2 HG02109.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.588-8455dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173283635 | |||||
| chr4:173283650
|
A | C | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.588-8458A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283650 | ||||||
| chr4:173283703
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0068 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.588-8405T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283703 | ||||||
| chr4:173283984
|
C | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0094others(12): Show | 15 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.588-8124C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283984 | ||||||
| chr4:173284115
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.588-7993T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284115 | ||||||
| chr4:173284227
|
C | T | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-7881C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284227 | ||||||
| chr4:173284387
|
T | G | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-7721T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284387 | ||||||
| chr4:173284392
|
A | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7716A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284392 | ||||||
| chr4:173284396
|
T | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-7712T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284396 | ||||||
| chr4:173284426
|
C | T | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588-7682C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284426 | ||||||
| chr4:173284427
|
A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.588-7681A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284427 | ||||||
| chr4:173284466
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-7642C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284466 | ||||||
| chr4:173284545
|
T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.588-7563T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284545 | ||||||
| chr4:173284583
|
C | T | 45 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7525C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284583 | ||||||
| chr4:173284681
|
A | T | 1 | a0001c0002t0001g0168 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.588-7427A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284681 | ||||||
| chr4:173284726
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588-7382A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284726 | ||||||
| chr4:173284729
|
A | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.588-7379A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284729 | ||||||
| chr4:173284791
|
T | TC | 45 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7317_588-7316i others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284791 | ||||||
| chr4:173284856
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7252A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284856 | ||||||
| chr4:173284859
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.588-7249C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284859 | ||||||
| chr4:173284904
|
T | G | 4 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0194others(1): Show | 4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7204T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284904 | ||||||
| chr4:173285332
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-6776A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285332 | ||||||
| chr4:173285641
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-6467C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285641 | ||||||
| chr4:173285645
|
T | C | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-6463T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285645 | ||||||
| chr4:173285763
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-6345G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285763 | ||||||
| chr4:173285824
|
T | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-6284T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285824 | ||||||
| chr4:173285849
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.588-6259T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285849 | ||||||
| chr4:173285852
|
C | T | 1 | a0001c0003t0002g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.588-6256C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285852 | ||||||
| chr4:173285895
|
T | G | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-6213T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285895 | ||||||
| chr4:173285981
|
G | A | 1 | a0001c0002t0001g0226 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.588-6127G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285981 | ||||||
| chr4:173286018
|
A | C | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-6090A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286018 | ||||||
| chr4:173286061
|
T | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588-6047T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286061 | ||||||
| chr4:173286137
|
T | G | 42 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(39): Show | 42 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-5971T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286137 | ||||||
| chr4:173287067
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0094others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-5041C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287067 | ||||||
| chr4:173287165
|
G | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-4943G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287165 | ||||||
| chr4:173287186
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-4922A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287186 | ||||||
| chr4:173287227
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.588-4881A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287227 | ||||||
| chr4:173287390
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.588-4718C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287390 | ||||||
| chr4:173287391
|
G | A | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-4717G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287391 | ||||||
| chr4:173287415
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.588-4693G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287415 | ||||||
| chr4:173287643
|
G | A | 3 | a0001c0001t0001g0063a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG01099.hp1 HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.588-4465G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287643 | ||||||
| chr4:173287907
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0116 | 2 | HG00597.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.588-4201A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287907 | ||||||
| chr4:173288086
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-4022A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288086 | ||||||
| chr4:173288140
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3968A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288140 | ||||||
| chr4:173288144
|
C | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 103 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.588-3964C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288144 | ||||||
| chr4:173288231
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0002g0192 | 2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.588-3877C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288231 | ||||||
| chr4:173288270
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-3838G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288270 | ||||||
| chr4:173288278
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3830A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288278 | ||||||
| chr4:173288282
|
C | CAAAAA | 31 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(28): Show | 31 | HG01106.hp1 HG01192.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.588-3807_588-3803d others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAA | 7 | a0001c0001t0002g0037a0001c0001t0002g0042a0001c0002t0002g0182others(4): Show | 7 | HG00423.hp1 HG00621.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-3808_588-3803d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0082others(9): Show | 12 | HG01081.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3811_588-3803d others(11): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(3): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0079others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3812_588-3803d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0091a0001c0002t0001g0173 | 3 | HG01192.hp1 HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588-3813_588-3803d others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0100a0001c0004t0001g0084 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.588-3814_588-3803d others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0265a0001c0005t0003g0095a0004c0011t0002g0180 | 3 | HG03471.hp1 HG06807.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.588-3816_588-3803d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(8): Show |
2 | a0001c0004t0001g0006a0001c0005t0003g0098 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.588-3817_588-3803d others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0266a0001c0002t0006g0170a0001c0002t0006g0171others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3818_588-3803d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(11): Show |
1 | a0001c0005t0003g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.588-3820_588-3803d others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.588-3821_588-3803d others(21): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588-3824_588-3803d others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(37): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
C | CAAAAAAA others(41): Show |
1 | a0001c0002t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(50): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
CA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.588-3803delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288282
|
CAA | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0155others(3): Show | 6 | HG02922.hp1 HG03516.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-3804_588-3803d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | |||||
| chr4:173288301
|
A | AAAAAAAA others(9): Show |
2 | a0001c0002t0001g0014a0001c0002t0001g0185 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.588-3803_588-3802i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288301 | |||||
| chr4:173288301
|
A | G | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588-3807A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288301 | ||||||
| chr4:173288306
|
G | A | 3 | a0001c0001t0001g0266a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.588-3802G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288306 | ||||||
| chr4:173288466
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.588-3642A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288466 | ||||||
| chr4:173288467
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.588-3641T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288467 | ||||||
| chr4:173288573
|
A | T | 1 | a0001c0002t0011g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.588-3535A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288573 | ||||||
| chr4:173288756
|
G | A | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3352G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288756 | ||||||
| chr4:173289010
|
C | A | 79 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0043others(76): Show | 79 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.588-3098C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289010 | ||||||
| chr4:173289080
|
G | A | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588-3028G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289080 | ||||||
| chr4:173289207
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.588-2901C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289207 | ||||||
| chr4:173289247
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.588-2861T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289247 | ||||||
| chr4:173289394
|
G | A | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-2714G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289394 | ||||||
| chr4:173289557
|
G | A | 1 | a0001c0005t0003g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.588-2551G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289557 | ||||||
| chr4:173289805
|
G | GT | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(8): Show | 11 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.588-2293dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173289805 | |||||
| chr4:173289920
|
C | A | 10 | a0001c0001t0001g0030a0001c0002t0001g0186a0001c0002t0001g0187others(7): Show | 10 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-2188C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289920 | ||||||
| chr4:173289940
|
G | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-2168G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289940 | ||||||
| chr4:173289981
|
A | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-2127A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289981 | ||||||
| chr4:173290134
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.588-1974G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290134 | ||||||
| chr4:173290238
|
GACTATGG others(9): Show |
G | 2 | a0001c0002t0001g0206a0001c0002t0001g0219 | 2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.588-1844_588-1829d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173290238 | |||||
| chr4:173290393
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.588-1715T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290393 | ||||||
| chr4:173290628
|
T | C | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-1480T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290628 | ||||||
| chr4:173290648
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-1460C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290648 | ||||||
| chr4:173290870
|
C | A | 50 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0061others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.588-1238C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290870 | ||||||
| chr4:173291119
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.588-989C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291119 | ||||||
| chr4:173291162
|
C | T | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-946C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291162 | ||||||
| chr4:173291169
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0094others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-939C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291169 | ||||||
| chr4:173291391
|
G | T | 1 | a0001c0002t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.588-717G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291391 | ||||||
| chr4:173291395
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588-713C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291395 | ||||||
| chr4:173291783
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(14): Show | 17 | HG01257.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-325G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291783 | ||||||
| chr4:173291794
|
G | GA | 14 | a0001c0001t0001g0050a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00738.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-298dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173291794 | |||||
| chr4:173291794
|
GA | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0094others(9): Show | 12 | HG01256.hp2 HG02055.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-298delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173291794 | |||||
| chr4:173291836
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.588-272C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291836 | ||||||
| chr4:173291846
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-262T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291846 | ||||||
| chr4:173291942
|
G | C | 1 | a0001c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-166G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291942 | ||||||
| chr4:173291962
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-146A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291962 | ||||||
| chr4:173292030
|
A | C | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-78A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173292030 | ||||||
| chr4:173292035
|
C | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-73C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173292035 | ||||||
| chr4:173292493
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.754+219G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292493 | ||||||
| chr4:173292563
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.754+289T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292563 | ||||||
| chr4:173292577
|
C | T | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.754+303C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292577 | ||||||
| chr4:173293106
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+832C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293106 | ||||||
| chr4:173293282
|
C | CT | 10 | a0001c0001t0004g0115a0001c0002t0001g0186a0001c0002t0001g0187others(7): Show | 10 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1018dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293282 | |||||
| chr4:173293320
|
T | C | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.754+1046T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293320 | ||||||
| chr4:173293347
|
TTTAGAG | T | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1075_754+1080d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293347 | |||||
| chr4:173293448
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754+1174A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293448 | ||||||
| chr4:173293532
|
T | TTTAAGA | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.754+1259_754+1260i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293532 | |||||
| chr4:173293589
|
A | G | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1315A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293589 | ||||||
| chr4:173293728
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.754+1454C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293728 | ||||||
| chr4:173293817
|
C | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+1543C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293817 | ||||||
| chr4:173293993
|
A | G | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.755-1403A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293993 | ||||||
| chr4:173294057
|
T | C | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1339T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294057 | ||||||
| chr4:173294243
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.755-1153C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294243 | ||||||
| chr4:173294274
|
C | CT | 6 | a0001c0001t0001g0158a0001c0002t0001g0207a0001c0002t0001g0216others(3): Show | 6 | HG01074.hp2 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-1109dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173294274 | |||||
| chr4:173294274
|
CTT | C | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.755-1110_755-1109d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173294274 | |||||
| chr4:173294343
|
G | A | 2 | a0001c0002t0002g0240a0001c0002t0002g0243 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.755-1053G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294343 | ||||||
| chr4:173294345
|
G | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.755-1051G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294345 | ||||||
| chr4:173295053
|
A | G | 54 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(51): Show | 54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.755-343A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295053 | ||||||
| chr4:173295259
|
C | A | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.755-137C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295259 | ||||||
| chr4:173295375
|
T | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.755-21T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295375 | ||||||
| chr4:173295596
|
C | T | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.885+70C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 4/11 | chr4 | 173295596 | ||||||
| chr4:173295971
|
A | G | 20 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.965+128A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173295971 | ||||||
| chr4:173296131
|
T | C | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.965+288T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296131 | ||||||
| chr4:173296254
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.965+411T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296254 | ||||||
| chr4:173296293
|
A | C | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+450A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296293 | ||||||
| chr4:173296437
|
C | T | 1 | a0001c0002t0001g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.965+594C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296437 | ||||||
| chr4:173296483
|
T | C | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.965+640T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296483 | ||||||
| chr4:173296525
|
A | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.965+682A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296525 | ||||||
| chr4:173296642
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.965+799C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296642 | ||||||
| chr4:173296647
|
A | C | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.965+804A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296647 | ||||||
| chr4:173296656
|
C | T | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+813C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296656 | ||||||
| chr4:173296927
|
A | G | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+1084A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296927 | ||||||
| chr4:173297172
|
A | G | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.966-943A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297172 | ||||||
| chr4:173297213
|
C | CT | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.966-891dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 173297213 | |||||
| chr4:173297245
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0044 | 3 | HG01993.hp2 HG02293.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.966-870T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297245 | ||||||
| chr4:173297248
|
TG | T | 15 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(12): Show | 15 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.966-866delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297248 | ||||||
| chr4:173297249
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.966-866G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297249 | ||||||
| chr4:173297274
|
T | G | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.966-841T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297274 | ||||||
| chr4:173297293
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.966-822G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297293 | ||||||
| chr4:173297414
|
A | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-701A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297414 | ||||||
| chr4:173297505
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.966-610A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297505 | ||||||
| chr4:173297639
|
C | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.966-476C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297639 | ||||||
| chr4:173297751
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.966-364T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297751 | ||||||
| chr4:173298430
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(28): Show | 31 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1148+133A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298430 | ||||||
| chr4:173298430
|
A | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1148+133A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298430 | ||||||
| chr4:173298439
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1148+142G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298439 | ||||||
| chr4:173298461
|
G | C | 5 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+164G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298461 | ||||||
| chr4:173298681
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+384C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298681 | ||||||
| chr4:173298702
|
A | T | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1148+405A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298702 | ||||||
| chr4:173299087
|
T | C | 3 | a0001c0003t0008g0248a0001c0003t0008g0254a0001c0003t0012g0255 | 3 | NA18975.hp1 NA19012.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1148+790T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299087 | ||||||
| chr4:173299180
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1148+883T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299180 | ||||||
| chr4:173299539
|
C | T | 54 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(51): Show | 54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1148+1242C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299539 | ||||||
| chr4:173299582
|
C | T | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1148+1285C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299582 | ||||||
| chr4:173299652
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1148+1355A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299652 | ||||||
| chr4:173299838
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+1541T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299838 | ||||||
| chr4:173299851
|
C | CA | 29 | a0001c0001t0001g0134a0001c0001t0005g0072a0001c0001t0005g0085others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1148+1565dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 173299851 | |||||
| chr4:173299857
|
A | C | 1 | a0001c0002t0001g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1148+1560A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299857 | ||||||
| chr4:173299877
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1148+1580G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299877 | ||||||
| chr4:173300008
|
A | G | 1 | a0001c0003t0002g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1148+1711A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300008 | ||||||
| chr4:173300176
|
G | A | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-1871G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300176 | ||||||
| chr4:173300335
|
C | T | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-1712C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300335 | ||||||
| chr4:173300589
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0001g0150a0001c0002t0001g0017others(1): Show | 4 | HG01934.hp1 NA18948.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149-1458G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300589 | ||||||
| chr4:173300751
|
C | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1149-1296C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300751 | ||||||
| chr4:173300778
|
A | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0265 | 3 | HG01192.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1149-1269A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300778 | ||||||
| chr4:173300937
|
C | G | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149-1110C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300937 | ||||||
| chr4:173300955
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0060others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-1092G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300955 | ||||||
| chr4:173301059
|
C | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-988C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301059 | ||||||
| chr4:173301083
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0154 | 2 | HG00558.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1149-964C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301083 | ||||||
| chr4:173301207
|
T | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1149-840T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301207 | ||||||
| chr4:173301345
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149-702C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301345 | ||||||
| chr4:173301567
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1149-480T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301567 | ||||||
| chr4:173301693
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1149-354G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301693 | ||||||
| chr4:173301830
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0043others(92): Show | 95 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1149-217G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301830 | ||||||
| chr4:173301834
|
C | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-213C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301834 | ||||||
| chr4:173302232
|
C | T | 5 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+68C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302232 | ||||||
| chr4:173302250
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+86A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302250 | ||||||
| chr4:173302504
|
A | G | 1 | a0001c0002t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1266+340A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302504 | ||||||
| chr4:173302518
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1266+354C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302518 | ||||||
| chr4:173302669
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1266+505C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302669 | ||||||
| chr4:173302839
|
A | T | 1 | a0001c0002t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1266+675A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302839 | ||||||
| chr4:173302914
|
A | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0062others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1266+750A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302914 | ||||||
| chr4:173302914
|
A | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+750A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302914 | ||||||
| chr4:173302921
|
G | A | 2 | a0001c0001t0001g0146a0001c0002t0001g0019 | 2 | HG00621.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1266+757G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302921 | ||||||
| chr4:173303019
|
A | G | 18 | a0001c0003t0002g0021a0001c0003t0002g0169a0001c0003t0002g0176others(15): Show | 18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266+855A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303019 | ||||||
| chr4:173303031
|
C | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+867C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303031 | ||||||
| chr4:173303032
|
T | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+868T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303032 | ||||||
| chr4:173303037
|
T | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+873T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303037 | ||||||
| chr4:173303039
|
C | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+875C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303039 | ||||||
| chr4:173303087
|
C | T | 1 | a0001c0002t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1267-909C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303087 | ||||||
| chr4:173303182
|
G | A | 2 | a0001c0005t0003g0093a0001c0005t0003g0095 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1267-814G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303182 | ||||||
| chr4:173303194
|
C | CA | 48 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0165others(45): Show | 48 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1267-789dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 173303194 | |||||
| chr4:173303223
|
A | G | 45 | a0001c0001t0001g0032a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00621.hp1 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.1267-773A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303223 | ||||||
| chr4:173303334
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1267-662A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303334 | ||||||
| chr4:173303513
|
C | T | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1267-483C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303513 | ||||||
| chr4:173303563
|
C | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267-433C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303563 | ||||||
| chr4:173303566
|
A | G | 10 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1267-430A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303566 | ||||||
| chr4:173303586
|
A | G | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1267-410A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303586 | ||||||
| chr4:173303609
|
A | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1267-387A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303609 | ||||||
| chr4:173303612
|
C | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267-384C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303612 | ||||||
| chr4:173303979
|
G | A | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1267-17G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303979 | ||||||
| chr4:173304386
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0004g0115a0001c0001t0004g0122 | 3 | HG01952.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1389+268G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304386 | ||||||
| chr4:173304400
|
TA | T | 6 | a0001c0001t0001g0054a0001c0001t0001g0117a0001c0001t0001g0141others(3): Show | 6 | HG00642.hp1 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+294delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173304400 | |||||
| chr4:173304434
|
T | C | 1 | a0001c0005t0003g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1389+316T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304434 | ||||||
| chr4:173304587
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1389+469C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304587 | ||||||
| chr4:173304686
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0083 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1389+568C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304686 | ||||||
| chr4:173304699
|
C | T | 2 | a0001c0002t0006g0170a0001c0002t0006g0171 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1389+581C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304699 | ||||||
| chr4:173304724
|
C | T | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1389+606C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304724 | ||||||
| chr4:173304733
|
A | C | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+615A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304733 | ||||||
| chr4:173304984
|
G | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+866G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304984 | ||||||
| chr4:173305113
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1389+995G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305113 | ||||||
| chr4:173305584
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1389+1466T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305584 | ||||||
| chr4:173305711
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1389+1593C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305711 | ||||||
| chr4:173306043
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1389+1925A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306043 | ||||||
| chr4:173306047
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+1929A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306047 | ||||||
| chr4:173306151
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1389+2033C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306151 | ||||||
| chr4:173306180
|
T | C | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2062T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306180 | ||||||
| chr4:173306298
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1389+2180A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306298 | ||||||
| chr4:173306356
|
T | TTTTC | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2244_1389+224 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173306356 | |||||
| chr4:173306451
|
T | C | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2333T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306451 | ||||||
| chr4:173306472
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1389+2354T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306472 | ||||||
| chr4:173306640
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+2522G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306640 | ||||||
| chr4:173306861
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1389+2743T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306861 | ||||||
| chr4:173307056
|
T | C | 1 | a0001c0004t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1389+2938T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307056 | ||||||
| chr4:173307247
|
G | T | 2 | a0001c0001t0010g0129a0001c0002t0010g0224 | 2 | HG00140.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1389+3129G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307247 | ||||||
| chr4:173307251
|
G | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+3133G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307251 | ||||||
| chr4:173307371
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1389+3253C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307371 | ||||||
| chr4:173307394
|
C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1389+3276C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307394 | ||||||
| chr4:173307442
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1389+3324C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307442 | ||||||
| chr4:173307492
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1389+3374G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307492 | ||||||
| chr4:173307876
|
G | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+3758G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307876 | ||||||
| chr4:173307947
|
C | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1389+3829C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307947 | ||||||
| chr4:173307977
|
G | A | 24 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(21): Show | 24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1389+3859G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307977 | ||||||
| chr4:173308409
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+4291C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308409 | ||||||
| chr4:173308433
|
G | T | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1389+4315G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308433 | ||||||
| chr4:173308486
|
C | T | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+4368C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308486 | ||||||
| chr4:173308534
|
A | G | 1 | a0001c0002t0001g0215 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1389+4416A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308534 | ||||||
| chr4:173308550
|
T | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1389+4432T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308550 | ||||||
| chr4:173308611
|
T | C | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1389+4493T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308611 | ||||||
| chr4:173308633
|
A | G | 1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1389+4515A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308633 | ||||||
| chr4:173308661
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+4543C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308661 | ||||||
| chr4:173308662
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0002t0001g0179others(2): Show | 5 | HG00642.hp1 HG01070.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+4544G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308662 | ||||||
| chr4:173308718
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0100 | 3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1389+4600C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308718 | ||||||
| chr4:173308721
|
A | G | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+4603A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308721 | ||||||
| chr4:173308772
|
G | A | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+4654G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308772 | ||||||
| chr4:173309199
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0100 | 3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-4759C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173309199 | ||||||
| chr4:173309217
|
G | A | 12 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-4741G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173309217 | ||||||
| chr4:173309883
|
CA | C | 13 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(10): Show | 13 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1390-4073delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173309883 | |||||
| chr4:173310097
|
A | C | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-3861A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310097 | ||||||
| chr4:173310541
|
G | A | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-3417G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310541 | ||||||
| chr4:173310828
|
C | A | 2 | a0001c0001t0001g0266a0001c0002t0001g0184 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1390-3130C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310828 | ||||||
| chr4:173310937
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-3021T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310937 | ||||||
| chr4:173311096
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0100 | 3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-2862C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311096 | ||||||
| chr4:173311115
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390-2843G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311115 | ||||||
| chr4:173311304
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1390-2654A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311304 | ||||||
| chr4:173311305
|
T | G | 1 | a0001c0002t0001g0194 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390-2653T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311305 | ||||||
| chr4:173311323
|
G | A | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-2635G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311323 | ||||||
| chr4:173311474
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1390-2484C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311474 | ||||||
| chr4:173311515
|
T | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0043others(84): Show | 87 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1390-2443T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311515 | ||||||
| chr4:173311719
|
G | A | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1390-2239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311719 | ||||||
| chr4:173311892
|
A | G | 3 | a0001c0002t0001g0017a0002c0007t0007g0177a0002c0007t0007g0178 | 3 | HG01934.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-2066A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311892 | ||||||
| chr4:173312761
|
A | G | 1 | a0001c0003t0002g0257 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1390-1197A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173312761 | ||||||
| chr4:173312788
|
A | G | 55 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(52): Show | 55 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.1390-1170A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173312788 | ||||||
| chr4:173313005
|
G | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-953G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313005 | ||||||
| chr4:173313070
|
T | TA | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0064others(29): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1390-888_1390-887i others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313070 | ||||||
| chr4:173313071
|
T | A | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-887T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313071 | ||||||
| chr4:173313086
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1390-872G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313086 | ||||||
| chr4:173313282
|
T | C | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-676T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313282 | ||||||
| chr4:173313290
|
C | G | 1 | a0003c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1390-668C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313290 | ||||||
| chr4:173313296
|
C | T | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1390-662C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313296 | ||||||
| chr4:173313379
|
G | T | 1 | a0001c0002t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1390-579G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313379 | ||||||
| chr4:173313405
|
C | CA | 53 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0039others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1390-546dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313405 | |||||
| chr4:173313458
|
C | T | 4 | a0001c0002t0013g0233a0001c0006t0001g0073a0001c0006t0001g0074others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-500C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313458 | ||||||
| chr4:173313570
|
C | CA | 11 | a0001c0001t0001g0004a0001c0002t0001g0173a0001c0002t0001g0174others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-372dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313570 | |||||
| chr4:173313570
|
CA | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0087a0001c0001t0002g0031others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-372delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313570 | |||||
| chr4:173313666
|
A | G | 5 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-292A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313666 | ||||||
| chr4:173313820
|
G | A | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-138G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313820 | ||||||
| chr4:173313901
|
A | G | 1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1390-57A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313901 | ||||||
| chr4:173313928
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1390-30G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313928 | ||||||
| chr4:173313928
|
G | GATAT | 10 | a0001c0001t0001g0032a0001c0001t0002g0026a0001c0001t0002g0027others(7): Show | 10 | HG00621.hp1 HG02040.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390-17_1390-14dup others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313928 | |||||
| chr4:173313941
|
A | AT | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-16dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313941 | |||||
| chr4:173313941
|
A | T | 17 | a0001c0003t0002g0021a0001c0003t0002g0176a0001c0003t0002g0181others(14): Show | 17 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-17A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313941 | ||||||
| chr4:173313943
|
A | ATAT | 13 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(10): Show | 13 | HG02451.hp1 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1390-14_1390-13ins others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313943 | |||||
| chr4:173313943
|
A | T | 33 | a0001c0001t0001g0266a0001c0001t0005g0072a0001c0001t0005g0085others(30): Show | 33 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1390-15A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313943 | ||||||
| chr4:173313944
|
T | TA | 5 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174others(2): Show | 5 | HG01891.hp1 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-14_1390-13ins others(1): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313944 | ||||||
| chr4:173313945
|
T | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0039 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1390-13T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313945 | ||||||
| chr4:173313946
|
T | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-12T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313946 | ||||||
| chr4:173313951
|
T | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.1390-7T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313951 | ||||||
| chr4:173314329
|
T | C | 45 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0165others(42): Show | 45 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1608+153T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314329 | ||||||
| chr4:173314445
|
T | A | 1 | a0001c0002t0001g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1608+269T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314445 | ||||||
| chr4:173314473
|
T | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1608+297T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314473 | ||||||
| chr4:173314662
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1608+486G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314662 | ||||||
| chr4:173314782
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1608+606T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314782 | ||||||
| chr4:173314852
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1608+676C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314852 | ||||||
| chr4:173314869
|
C | G | 1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+693C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314869 | ||||||
| chr4:173315046
|
GATA | G | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1608+873_1608+875d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173315046 | |||||
| chr4:173315270
|
T | G | 9 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172others(6): Show | 9 | HG01346.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1608+1094T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315270 | ||||||
| chr4:173315353
|
G | A | 1 | a0001c0002t0001g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1608+1177G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315353 | ||||||
| chr4:173315559
|
G | A | 5 | a0001c0001t0003g0078a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+1383G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315559 | ||||||
| chr4:173315602
|
C | G | 42 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(39): Show | 42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1608+1426C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315602 | ||||||
| chr4:173315667
|
C | CTTAT | 54 | a0001c0001t0001g0032a0001c0001t0001g0102a0001c0001t0002g0022others(51): Show | 54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1608+1494_1608+149 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173315667 | |||||
| chr4:173315697
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1608+1521A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315697 | ||||||
| chr4:173315885
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1709A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315885 | ||||||
| chr4:173315910
|
C | T | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1609-1724C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315910 | ||||||
| chr4:173315940
|
C | G | 1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-1694C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315940 | ||||||
| chr4:173316038
|
AGAGT | A | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0002t0001g0173others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1609-1593_1609-159 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173316038 | |||||
| chr4:173316065
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1609-1569A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316065 | ||||||
| chr4:173316171
|
GGCCTCAC others(8): Show |
G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1609-1460_1609-144 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173316171 | |||||
| chr4:173316221
|
C | T | 1 | a0001c0005t0003g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1609-1413C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316221 | ||||||
| chr4:173316291
|
G | C | 1 | a0001c0001t0002g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1609-1343G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316291 | ||||||
| chr4:173316420
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0002t0001g0173others(1): Show | 4 | HG01891.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1214T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316420 | ||||||
| chr4:173316654
|
T | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1609-980T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316654 | ||||||
| chr4:173316838
|
C | T | 1 | a0001c0002t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1609-796C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316838 | ||||||
| chr4:173316897
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1609-737T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316897 | ||||||
| chr4:173317005
|
A | C | 1 | a0001c0001t0011g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1609-629A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317005 | ||||||
| chr4:173317199
|
C | T | 1 | a0001c0002t0013g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-435C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317199 | ||||||
| chr4:173317449
|
C | A | 1 | a0001c0002t0001g0225 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1609-185C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317449 | ||||||
| chr4:173317451
|
T | A | 2 | a0001c0002t0001g0200a0001c0002t0001g0235 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1609-183T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317451 | ||||||
| chr4:173317769
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0265 | 3 | HG01192.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1707+37A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173317769 | ||||||
| chr4:173317889
|
A | G | 51 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(48): Show | 51 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.1707+157A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173317889 | ||||||
| chr4:173318106
|
A | G | 3 | a0001c0002t0006g0170a0001c0002t0006g0171a0001c0002t0006g0172 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1708-325A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318106 | ||||||
| chr4:173318226
|
G | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG01884.hp1 HG02897.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-205G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318226 | ||||||
| chr4:173318396
|
C | T | 1 | a0001c0001t0002g0031 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1708-35C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318396 | ||||||
| chr4:173318786
|
G | A | 43 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(40): Show | 43 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1836+227G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173318786 | ||||||
| chr4:173319057
|
G | A | 3 | a0001c0001t0001g0091a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+498G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319057 | ||||||
| chr4:173319109
|
G | A | 5 | a0001c0004t0001g0006a0001c0004t0001g0076a0001c0004t0001g0077others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+550G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319109 | ||||||
| chr4:173319275
|
T | TAA | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+722_1836+723d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 173319275 | |||||
| chr4:173319526
|
CA | C | 45 | a0001c0001t0001g0032a0001c0001t0002g0022a0001c0001t0002g0023others(42): Show | 45 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1836+976delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 173319526 | |||||
| chr4:173319818
|
A | G | 9 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1836+1259A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319818 | ||||||
| chr4:173320383
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1837-1197A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320383 | ||||||
| chr4:173320443
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1837-1137A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320443 | ||||||
| chr4:173320542
|
T | C | 53 | a0001c0001t0001g0102a0001c0001t0002g0022a0001c0001t0002g0023others(50): Show | 53 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1837-1038T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320542 | ||||||
| chr4:173320614
|
G | A | 7 | a0001c0001t0005g0072a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-966G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320614 | ||||||
| chr4:173320619
|
C | T | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1837-961C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320619 | ||||||
| chr4:173320656
|
A | C | 2 | a0001c0001t0001g0150a0001c0002t0001g0017 | 2 | HG01934.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1837-924A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320656 | ||||||
| chr4:173320827
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1837-753C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320827 | ||||||
| chr4:173320939
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1837-641G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320939 | ||||||
| chr4:173321044
|
C | T | 1 | a0001c0002t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1837-536C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321044 | ||||||
| chr4:173321075
|
A | C | 1 | a0001c0002t0001g0226 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1837-505A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321075 | ||||||
| chr4:173321126
|
T | C | 53 | a0001c0001t0001g0102a0001c0001t0002g0022a0001c0001t0002g0023others(50): Show | 53 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1837-454T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321126 | ||||||
| chr4:173321147
|
A | C | 43 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(40): Show | 43 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1837-433A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321147 | ||||||
| chr4:173321167
|
G | A | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837-413G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321167 | ||||||
| chr4:173321516
|
G | A | 2 | a0002c0007t0007g0177a0002c0007t0007g0178 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1837-64G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321516 |