| geneid | 145173 |
|---|---|
| ensemblid | ENSG00000187676.8 |
| hgncid | 20207 |
| symbol | B3GLCT |
| name | beta 3-glucosyltransferase |
| refseq_nuc | NM_194318.4 |
| refseq_prot | NP_919299.3 |
| ensembl_nuc | ENST00000343307.5 |
| ensembl_prot | ENSP00000343002.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 31199975 |
| end | 31332276 |
| strand | + |
| ver | v1.2 |
| region | chr13:31199975-31332276 |
| region5000 | chr13:31194975-31337276 |
| regionname0 | B3GLCT_chr13_31199975_31332276 |
| regionname5000 | B3GLCT_chr13_31194975_31337276 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 498 | 140 | 22 | 33 | 65 | 5 | 15 | 44 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002 | 1/1 | 498 | 118 | 56 | 15 | 32 | 3 | 10 | 27 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0003 | 0/0 | 498 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0004 | 0/0 | 498 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0005 | 0/0 | 338 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0006 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0007 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| 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 | 1497 | 139 | 21 | 33 | 65 | 5 | 15 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0002 | 0/1 | 1497 | 106 | 47 | 14 | 32 | 2 | 10 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0003 | 1/0 | 1497 | 8 | 7 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0004 | 0/0 | 1497 | 3 | 0 | 3 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0005 | 0/0 | 1497 | 3 | 1 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0006 | 0/0 | 1497 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0007 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0008 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0009 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0010 | 0/0 | 1497 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0011 | 0/0 | 1497 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0012 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| c0013 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2713 | 75 | 14 | 21 | 30 | 2 | 8 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0002 | 0/0 | 2713 | 44 | 21 | 1 | 18 | 0 | 4 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0003 | 1/1 | 2719 | 42 | 20 | 12 | 0 | 3 | 5 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0004 | 0/0 | 2719 | 33 | 11 | 7 | 14 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0005 | 0/0 | 2713 | 16 | 1 | 3 | 8 | 1 | 3 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0006 | 0/0 | 2719 | 13 | 0 | 2 | 10 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0007 | 0/0 | 2713 | 9 | 0 | 5 | 0 | 2 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0008 | 0/0 | 2714 | 7 | 0 | 0 | 7 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0009 | 0/0 | 2720 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0010 | 0/0 | 2713 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0011 | 0/0 | 2710 | 3 | 3 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0012 | 0/0 | 2719 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0013 | 0/0 | 2720 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0014 | 0/0 | 2713 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0015 | 0/0 | 2714 | 2 | 1 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0016 | 0/0 | 2713 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0017 | 0/0 | 2719 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0018 | 0/0 | 2719 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0019 | 0/0 | 2719 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0020 | 0/0 | 2719 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0021 | 0/0 | 2713 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0022 | 0/0 | 2713 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0023 | 0/0 | 2720 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0024 | 0/0 | 2713 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| t0025 | 0/0 | 2713 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| 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 | 1497 | 139 | 21 | 33 | 65 | 5 | 15 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0013 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002 | 0/1 | 1497 | 106 | 47 | 14 | 32 | 2 | 10 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0003 | 1/0 | 1497 | 8 | 7 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0007 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0008 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0010 | 0/0 | 1497 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0011 | 0/0 | 1497 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0003c0004 | 0/0 | 1497 | 3 | 0 | 3 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0004c0005 | 0/0 | 1497 | 3 | 1 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0005c0006 | 0/0 | 1497 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0006c0012 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0007c0009 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4209 | 70 | 11 | 20 | 30 | 2 | 7 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0004 | 0/0 | 4215 | 21 | 7 | 1 | 12 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0005 | 0/0 | 4209 | 16 | 1 | 3 | 8 | 1 | 3 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0006 | 0/0 | 4215 | 12 | 0 | 2 | 9 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0007 | 0/0 | 4209 | 9 | 0 | 5 | 0 | 2 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0010 | 0/0 | 4209 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0014 | 0/0 | 4209 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0015 | 0/0 | 4210 | 2 | 1 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0022 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0024 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0001t0025 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0001c0013t0001 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0001 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0002 | 0/0 | 4209 | 40 | 17 | 1 | 18 | 0 | 4 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0003 | 0/1 | 4215 | 34 | 16 | 10 | 0 | 2 | 5 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0004 | 0/0 | 4215 | 7 | 4 | 2 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0006 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0008 | 0/0 | 4210 | 7 | 0 | 0 | 7 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0009 | 0/0 | 4216 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0011 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0012 | 0/0 | 4215 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0013 | 0/0 | 4216 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0016 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0017 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0018 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0019 | 0/0 | 4215 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0002t0020 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0003t0002 | 0/0 | 4209 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0003t0003 | 1/0 | 4215 | 5 | 4 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0003t0021 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0007t0023 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0008t0002 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0010t0003 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0002c0011t0004 | 0/0 | 4215 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0003c0004t0004 | 0/0 | 4215 | 3 | 0 | 3 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0004c0005t0001 | 0/0 | 4209 | 3 | 1 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0005c0006t0003 | 0/0 | 4215 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0006c0012t0004 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| a0007c0009t0002 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | copy fasta | chr13 | 31194975 | 31337276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0014g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0014g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0015g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0015g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0024g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0025g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0013t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0018g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0019g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0021g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0007t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0008t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0010t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0011t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0004t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0004t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0004t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0005c0006t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0005c0006t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0006c0012t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0007c0009t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0010 | t0003 | g0010 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0200 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00621 | hp1 | a0002 | c0002 | t0008 | g0145 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0230 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0109 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0088 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00741 | hp2 | a0004 | c0005 | t0001 | g0073 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01071 | hp2 | a0003 | c0004 | t0004 | g0205 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0207 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01106 | hp2 | a0002 | c0011 | t0004 | g0181 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01167 | hp1 | a0003 | c0004 | t0004 | g0208 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01169 | hp1 | a0003 | c0004 | t0004 | g0209 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0023 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0183 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0236 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0243 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0186 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01256 | hp2 | a0005 | c0006 | t0003 | g0226 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01258 | hp1 | a0005 | c0006 | t0003 | g0227 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0028 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0254 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0244 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0240 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0247 | EUR | IBS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0020 | EUR | IBS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01891 | hp1 | a0002 | c0008 | t0002 | g0063 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01943 | hp2 | a0002 | c0002 | t0019 | g0251 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0147 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0245 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0238 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02015 | hp1 | a0002 | c0002 | t0009 | g0211 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0198 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02055 | hp1 | a0001 | c0013 | t0001 | g0262 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0123 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0216 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0249 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02148 | hp2 | a0001 | c0001 | t0014 | g0036 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | CDX | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02280 | hp1 | a0002 | c0002 | t0011 | g0006 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0067 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0094 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02451 | hp2 | a0002 | c0003 | t0021 | g0068 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02572 | hp2 | a0002 | c0002 | t0011 | g0005 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02615 | hp1 | a0002 | c0003 | t0002 | g0171 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02615 | hp2 | a0002 | c0002 | t0013 | g0008 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0248 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02630 | hp2 | a0002 | c0002 | t0012 | g0174 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0255 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0144 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0257 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02717 | hp2 | a0002 | c0007 | t0023 | g0004 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0012 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0105 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02818 | hp2 | a0007 | c0009 | t0002 | g0264 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02886 | hp1 | a0002 | c0002 | t0011 | g0007 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02896 | hp2 | a0001 | c0001 | t0025 | g0261 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0265 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0180 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0033 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03098 | hp1 | a0002 | c0002 | t0004 | g0011 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03130 | hp1 | a0002 | c0002 | t0018 | g0253 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03139 | hp2 | a0002 | c0002 | t0012 | g0176 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0177 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03195 | hp2 | a0002 | c0002 | t0020 | g0239 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0263 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03239 | hp1 | a0002 | c0002 | t0017 | g0019 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0219 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0172 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0079 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0182 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0246 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0250 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0258 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0074 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0078 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0214 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0197 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0066 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0077 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0234 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0021 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0034 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0099 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18963 | hp1 | a0002 | c0002 | t0009 | g0013 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18968 | hp1 | a0002 | c0002 | t0008 | g0125 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0081 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18975 | hp1 | a0002 | c0002 | t0016 | g0142 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18978 | hp1 | a0002 | c0002 | t0008 | g0060 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18984 | hp2 | a0006 | c0012 | t0004 | g0059 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18990 | hp2 | a0002 | c0002 | t0006 | g0141 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18997 | hp1 | a0002 | c0002 | t0009 | g0212 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18997 | hp2 | a0002 | c0002 | t0008 | g0083 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0221 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19030 | hp2 | a0002 | c0003 | t0002 | g0162 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0228 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19056 | hp1 | a0001 | c0001 | t0022 | g0050 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19058 | hp1 | a0002 | c0002 | t0008 | g0097 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19060 | hp2 | a0002 | c0002 | t0008 | g0096 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19072 | hp2 | a0002 | c0002 | t0008 | g0143 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19081 | hp1 | a0002 | c0002 | t0009 | g0210 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19082 | hp1 | a0001 | c0001 | t0010 | g0114 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0179 | AFR | ASW | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ASW | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0025 | EUR | TSI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0027 | EUR | TSI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02109 | hp2 | a0002 | c0003 | t0003 | g0188 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02486 | hp1 | a0004 | c0005 | t0001 | g0072 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0222 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02559 | hp2 | a0002 | c0002 | t0013 | g0191 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0241 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG06807 | hp1 | a0002 | c0003 | t0003 | g0026 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0259 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0220 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0229 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0260 | REF | REF | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0003 | g0213 | REF | REF | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31247957
|
C | A | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.450C>A | p.Asp150Glu | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/15 | 560/4215 | 450/1497 | 150/498 | chr13 | 31247957 | ||
| chr13:31274581
|
G | A | 1 | a0003 | 3 | HG01071.hp2 HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.733G>A | p.Val245Met | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/15 | 843/4215 | 733/1497 | 245/498 | chr13 | 31274581 | ||
| chr13:31284699
|
A | T | 1 | a0006 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.902A>T | p.Tyr301Phe | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/15 | 1012/4215 | 902/1497 | 301/498 | chr13 | 31284699 | ||
| chr13:31286770
|
C | T | 1 | a0005 | 2 | HG01256.hp2 HG01258.hp1 |
stop_gained | HIGH | c.1015C>T | p.Gln339* | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/15 | 1125/4215 | 1015/1497 | 339/498 | chr13 | 31286770 | ||
| chr13:31317606
|
G | A | 1 | a0004 | 3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.1105G>A | p.Gly369Ser | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1215/4215 | 1105/1497 | 369/498 | chr13 | 31317606 | ||
| chr13:31317609
|
G | A | 4 | a0001a0003a0004others(1): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
missense_variant | MODERATE | c.1108G>A | p.Glu370Lys | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1218/4215 | 1108/1497 | 370/498 | chr13 | 31317609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200123
|
G | C | 1 | a0002c0007 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.39G>C | p.Pro13Pro | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/15 | 149/4215 | 39/1497 | 13/498 | chr13 | 31200123 | ||
| chr13:31247049
|
T | C | 1 | a0002c0008 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.297T>C | p.His99His | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/15 | 407/4215 | 297/1497 | 99/498 | chr13 | 31247049 | ||
| chr13:31247855
|
T | C | 10 | a0001c0001a0002c0002a0002c0007others(7): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
splice_region_variant&synonymous_variant | LOW | c.348T>C | p.His116His | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/15 | 458/4215 | 348/1497 | 116/498 | chr13 | 31247855 | ||
| chr13:31317635
|
C | T | 1 | a0002c0011 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.1134C>T | p.Tyr378Tyr | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1244/4215 | 1134/1497 | 378/498 | chr13 | 31317635 | ||
| chr13:31329542
|
A | G | 1 | a0002c0010 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1371A>G | p.Gln457Gln | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1481/4215 | 1371/1497 | 457/498 | chr13 | 31329542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200049
|
C | G | 1 | a0001c0001t0025 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/15 | 36 | chr13 | 31200049 | |||||
| chr13:31329697
|
G | T | 11 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(8): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*29G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 29 | chr13 | 31329697 | |||||
| chr13:31329704
|
A | G | 1 | a0001c0001t0007 | 9 | HG00738.hp1 HG01175.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*36A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 36 | chr13 | 31329704 | |||||
| chr13:31330072
|
G | A | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 404 | chr13 | 31330072 | |||||
| chr13:31330079
|
T | A | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 411 | chr13 | 31330079 | |||||
| chr13:31330083
|
A | G | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 415 | chr13 | 31330083 | |||||
| chr13:31330190
|
G | A | 1 | a0002c0002t0017 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 522 | chr13 | 31330190 | |||||
| chr13:31330217
|
ACAT | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*553_*555delCAT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 553 | INFO_REALIGN_3_PRIME | chr13 | 31330217 | ||||
| chr13:31330305
|
A | G | 1 | a0002c0002t0013 | 2 | HG02559.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*637A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 637 | chr13 | 31330305 | |||||
| chr13:31330324
|
C | T | 1 | a0002c0007t0023 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 656 | chr13 | 31330324 | |||||
| chr13:31330351
|
G | A | 1 | a0002c0002t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 683 | chr13 | 31330351 | |||||
| chr13:31330490
|
T | A | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 822 | chr13 | 31330490 | |||||
| chr13:31330540
|
G | GT | 21 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(18): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*888dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | INFO_REALIGN_3_PRIME | chr13 | 31330540 | ||||
| chr13:31330540
|
G | GTT | 2 | a0001c0001t0015a0002c0002t0008 | 9 | HG00621.hp1 HG02145.hp2 HG02735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*887_*888dupTT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | INFO_REALIGN_3_PRIME | chr13 | 31330540 | ||||
| chr13:31330557
|
A | G | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(20): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*889A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | chr13 | 31330557 | |||||
| chr13:31330557
|
A | T | 2 | a0001c0001t0006a0002c0002t0006 | 13 | HG00558.hp1 HG01943.hp1 HG01952.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*889A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | chr13 | 31330557 | |||||
| chr13:31330638
|
G | C | 1 | a0002c0002t0009 | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*970G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 970 | chr13 | 31330638 | |||||
| chr13:31330865
|
A | T | 1 | a0002c0002t0013 | 2 | HG02559.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1197 | chr13 | 31330865 | |||||
| chr13:31330874
|
T | C | 1 | a0002c0003t0021 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1206 | chr13 | 31330874 | |||||
| chr13:31330997
|
T | A | 1 | a0002c0002t0012 | 2 | HG02630.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1329T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1329 | chr13 | 31330997 | |||||
| chr13:31331008
|
G | A | 1 | a0002c0002t0019 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1340 | chr13 | 31331008 | |||||
| chr13:31331012
|
C | T | 1 | a0002c0002t0020 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1344 | chr13 | 31331012 | |||||
| chr13:31331184
|
A | G | 1 | a0002c0002t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1516 | chr13 | 31331184 | |||||
| chr13:31331312
|
A | T | 8 | a0001c0001t0004a0001c0001t0006a0002c0002t0004others(5): Show | 48 | HG00558.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1644A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1644 | chr13 | 31331312 | |||||
| chr13:31331361
|
G | C | 1 | a0001c0001t0005 | 16 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1693G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1693 | chr13 | 31331361 | |||||
| chr13:31331412
|
GCCTTCTA | G | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1746_*1752delCTTC others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1746 | INFO_REALIGN_3_PRIME | chr13 | 31331412 | ||||
| chr13:31331420
|
C | T | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1752C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1752 | chr13 | 31331420 | |||||
| chr13:31331469
|
A | G | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(21): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1801A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1801 | chr13 | 31331469 | |||||
| chr13:31331504
|
G | A | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(21): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1836 | chr13 | 31331504 | |||||
| chr13:31331735
|
A | G | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2067A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2067 | chr13 | 31331735 | |||||
| chr13:31331750
|
G | T | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(9): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2082G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2082 | chr13 | 31331750 | |||||
| chr13:31331769
|
T | C | 1 | a0001c0001t0010 | 4 | HG00558.hp2 HG00673.hp2 NA19070.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2101T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2101 | chr13 | 31331769 | |||||
| chr13:31331805
|
T | C | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(17): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2137T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2137 | chr13 | 31331805 | |||||
| chr13:31331856
|
T | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2188 | chr13 | 31331856 | |||||
| chr13:31332004
|
A | C | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(19): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*2336A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2336 | chr13 | 31332004 | |||||
| chr13:31332114
|
A | G | 1 | a0001c0001t0014 | 2 | HG01255.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2446A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2446 | chr13 | 31332114 | |||||
| chr13:31332154
|
T | C | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(19): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*2486T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2486 | chr13 | 31332154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200283
|
C | G | 4 | a0002c0002t0002g0263a0002c0002t0002g0266a0002c0002t0003g0265others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+129C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200283 | ||||||
| chr13:31200594
|
C | T | 26 | a0001c0001t0001g0242a0001c0001t0001g0256a0001c0001t0005g0254others(23): Show | 27 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.70+440C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200594 | ||||||
| chr13:31200681
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70+527C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200681 | ||||||
| chr13:31200938
|
C | T | 1 | a0002c0002t0003g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.70+784C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200938 | ||||||
| chr13:31200990
|
T | A | 1 | a0001c0001t0010g0003 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.70+836T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200990 | ||||||
| chr13:31201010
|
T | TA | 167 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.70+871dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31201010 | |||||
| chr13:31201237
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+1083A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201237 | ||||||
| chr13:31201405
|
A | G | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70+1251A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201405 | ||||||
| chr13:31201637
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.70+1483T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201637 | ||||||
| chr13:31201641
|
C | A | 5 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1487C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201641 | ||||||
| chr13:31201726
|
A | G | 1 | a0002c0002t0002g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70+1572A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201726 | ||||||
| chr13:31201842
|
A | C | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.70+1688A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201842 | ||||||
| chr13:31201926
|
C | A | 66 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.70+1772C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201926 | ||||||
| chr13:31201926
|
C | G | 199 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(196): Show | 201 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.70+1772C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201926 | ||||||
| chr13:31202068
|
C | A | 1 | a0002c0002t0003g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+1914C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202068 | ||||||
| chr13:31202142
|
A | G | 1 | a0002c0002t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+1988A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202142 | ||||||
| chr13:31202161
|
A | G | 20 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(17): Show | 21 | HG00140.hp2 HG00735.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+2007A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202161 | ||||||
| chr13:31202281
|
C | T | 125 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(122): Show | 126 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.70+2127C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202281 | ||||||
| chr13:31202337
|
G | A | 1 | a0001c0001t0005g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.70+2183G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202337 | ||||||
| chr13:31202345
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70+2191C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202345 | ||||||
| chr13:31202418
|
G | A | 1 | a0002c0002t0003g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.70+2264G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202418 | ||||||
| chr13:31202601
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+2447G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202601 | ||||||
| chr13:31202698
|
C | A | 30 | a0001c0001t0001g0069a0001c0001t0001g0242a0001c0001t0001g0256others(27): Show | 31 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.70+2544C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202698 | ||||||
| chr13:31202861
|
A | G | 71 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.70+2707A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202861 | ||||||
| chr13:31202875
|
A | C | 1 | a0002c0002t0002g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.70+2721A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202875 | ||||||
| chr13:31202952
|
A | G | 1 | a0001c0001t0005g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70+2798A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202952 | ||||||
| chr13:31202983
|
C | T | 1 | a0002c0002t0002g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70+2829C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202983 | ||||||
| chr13:31203357
|
T | C | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.70+3203T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203357 | ||||||
| chr13:31203400
|
A | G | 102 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(99): Show | 102 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.70+3246A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203400 | ||||||
| chr13:31203428
|
A | G | 102 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(99): Show | 102 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.70+3274A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203428 | ||||||
| chr13:31203429
|
G | A | 4 | a0001c0001t0001g0069a0002c0003t0002g0162a0002c0003t0002g0171others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3275G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203429 | ||||||
| chr13:31203468
|
C | T | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.70+3314C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203468 | ||||||
| chr13:31203583
|
A | G | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+3429A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203583 | ||||||
| chr13:31203665
|
T | A | 1 | a0002c0002t0002g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.70+3511T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203665 | ||||||
| chr13:31203675
|
A | G | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.70+3521A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203675 | ||||||
| chr13:31203718
|
A | G | 98 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(95): Show | 98 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.70+3564A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203718 | ||||||
| chr13:31203823
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.70+3669T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203823 | ||||||
| chr13:31203982
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.70+3828A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203982 | ||||||
| chr13:31204026
|
A | T | 33 | a0001c0001t0001g0069a0001c0001t0001g0242a0001c0001t0001g0256others(30): Show | 34 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.70+3872A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204026 | ||||||
| chr13:31204069
|
G | T | 3 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0008t0002g0063 | 3 | HG01891.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.70+3915G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204069 | ||||||
| chr13:31204161
|
G | C | 1 | a0002c0002t0020g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+4007G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204161 | ||||||
| chr13:31204391
|
C | A | 1 | a0002c0010t0003g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.70+4237C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204391 | ||||||
| chr13:31204395
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+4241G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204395 | ||||||
| chr13:31204793
|
T | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+4639T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204793 | ||||||
| chr13:31204859
|
A | G | 5 | a0001c0001t0005g0206a0001c0001t0005g0207a0003c0004t0004g0205others(2): Show | 5 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+4705A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204859 | ||||||
| chr13:31204881
|
A | T | 1 | a0002c0002t0002g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.70+4727A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204881 | ||||||
| chr13:31205136
|
A | G | 1 | a0002c0002t0002g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.70+4982A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205136 | ||||||
| chr13:31205245
|
T | G | 5 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+5091T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205245 | ||||||
| chr13:31205252
|
T | G | 1 | a0002c0002t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70+5098T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205252 | ||||||
| chr13:31205372
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+5218C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205372 | ||||||
| chr13:31205428
|
G | A | 101 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(98): Show | 101 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.70+5274G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205428 | ||||||
| chr13:31205578
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70+5424C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205578 | ||||||
| chr13:31205745
|
T | G | 4 | a0002c0002t0002g0263a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+5591T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205745 | ||||||
| chr13:31205882
|
A | G | 1 | a0002c0002t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+5728A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205882 | ||||||
| chr13:31205946
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70+5792T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205946 | ||||||
| chr13:31206126
|
G | C | 1 | a0002c0002t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.70+5972G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206126 | ||||||
| chr13:31206523
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.70+6369G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206523 | ||||||
| chr13:31206584
|
C | CA | 11 | a0001c0001t0001g0217a0001c0001t0004g0163a0001c0001t0004g0164others(8): Show | 11 | HG02145.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+6449dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31206584 | |||||
| chr13:31206584
|
CA | C | 188 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(185): Show | 188 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.70+6449delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31206584 | |||||
| chr13:31206605
|
G | T | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.70+6451G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206605 | ||||||
| chr13:31206611
|
G | A | 2 | a0002c0002t0004g0011a0003c0004t0004g0205 | 2 | HG01071.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.70+6457G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206611 | ||||||
| chr13:31206616
|
T | C | 1 | a0002c0002t0003g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70+6462T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206616 | ||||||
| chr13:31206724
|
G | A | 1 | a0002c0002t0002g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70+6570G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206724 | ||||||
| chr13:31206826
|
C | A | 4 | a0002c0002t0002g0263a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+6672C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206826 | ||||||
| chr13:31206851
|
G | A | 39 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0242others(36): Show | 40 | HG01106.hp2 HG01123.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.70+6697G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206851 | ||||||
| chr13:31207048
|
G | A | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+6894G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207048 | ||||||
| chr13:31207241
|
T | C | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+7087T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207241 | ||||||
| chr13:31207275
|
C | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0146a0001c0001t0001g0148others(13): Show | 16 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.70+7121C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207275 | ||||||
| chr13:31207287
|
A | AT | 66 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.70+7145dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31207287 | |||||
| chr13:31207558
|
T | C | 10 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(7): Show | 10 | HG01106.hp2 HG02630.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+7404T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207558 | ||||||
| chr13:31207625
|
G | A | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-7426G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207625 | ||||||
| chr13:31208096
|
TGTACTCT others(14): Show |
T | 1 | a0001c0001t0001g0232 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-6943_71-6923del others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208096 | |||||
| chr13:31208145
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0004g0173a0002c0002t0002g0235 | 3 | HG01891.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.71-6906A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208145 | ||||||
| chr13:31208148
|
A | T | 2 | a0002c0002t0003g0079a0002c0002t0003g0258 | 2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.71-6903A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208148 | ||||||
| chr13:31208170
|
C | CCGGGTCT others(3): Show |
1 | a0002c0002t0008g0083 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.71-6879_71-6870dup others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208170 | |||||
| chr13:31208172
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.71-6879G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208172 | ||||||
| chr13:31208243
|
A | G | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-6808A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208243 | ||||||
| chr13:31208289
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-6762T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208289 | ||||||
| chr13:31208342
|
G | A | 3 | a0002c0002t0003g0240a0002c0002t0013g0008a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-6709G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208342 | ||||||
| chr13:31208407
|
C | T | 2 | a0002c0002t0002g0266a0002c0002t0003g0265 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.71-6644C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208407 | ||||||
| chr13:31208437
|
A | G | 37 | a0001c0001t0001g0062a0001c0001t0001g0117a0001c0001t0001g0118others(34): Show | 37 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-6614A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208437 | ||||||
| chr13:31208552
|
T | G | 4 | a0002c0003t0002g0162a0002c0003t0002g0171a0002c0003t0021g0068others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6499T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208552 | ||||||
| chr13:31208561
|
G | A | 50 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0085others(47): Show | 50 | HG00609.hp1 HG01192.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.71-6490G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208561 | ||||||
| chr13:31208594
|
GC | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0051others(82): Show | 86 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.71-6455delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208594 | |||||
| chr13:31208619
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-6432G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208619 | ||||||
| chr13:31208619
|
G | GC | 50 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0070others(47): Show | 51 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-6420dupC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | |||||
| chr13:31208619
|
G | GCC | 22 | a0001c0001t0001g0086a0001c0001t0001g0192a0001c0001t0001g0242others(19): Show | 23 | HG00609.hp2 HG00735.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-6421_71-6420dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | |||||
| chr13:31208619
|
GC | G | 16 | a0001c0001t0004g0032a0001c0001t0010g0003a0001c0001t0010g0109others(13): Show | 16 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-6420delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | |||||
| chr13:31208626
|
C | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0117a0001c0001t0001g0118others(7): Show | 10 | HG02027.hp2 HG02129.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-6425C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208626 | ||||||
| chr13:31208626
|
C | CCT | 86 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(83): Show | 86 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.71-6424_71-6423ins others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208626 | |||||
| chr13:31208626
|
C | T | 1 | a0002c0002t0003g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-6425C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208626 | ||||||
| chr13:31208627
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71-6424C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208627 | ||||||
| chr13:31208631
|
C | T | 97 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(94): Show | 97 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.71-6420C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208631 | ||||||
| chr13:31208730
|
G | A | 4 | a0001c0001t0001g0175a0002c0002t0003g0220a0002c0002t0012g0174others(1): Show | 4 | HG02630.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6321G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208730 | ||||||
| chr13:31208845
|
A | G | 244 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.71-6206A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208845 | ||||||
| chr13:31208879
|
G | A | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-6172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208879 | ||||||
| chr13:31209090
|
C | T | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.71-5961C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209090 | ||||||
| chr13:31209094
|
G | C | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-5957G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209094 | ||||||
| chr13:31209200
|
A | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5851A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209200 | ||||||
| chr13:31209227
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5824G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209227 | ||||||
| chr13:31209344
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5707C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209344 | ||||||
| chr13:31209471
|
A | G | 1 | a0001c0001t0005g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.71-5580A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209471 | ||||||
| chr13:31209497
|
C | T | 20 | a0001c0001t0001g0022a0001c0001t0001g0192a0001c0001t0001g0193others(17): Show | 21 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-5554C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209497 | ||||||
| chr13:31209571
|
A | T | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-5480A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209571 | ||||||
| chr13:31209840
|
C | G | 223 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.71-5211C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209840 | ||||||
| chr13:31210003
|
T | G | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71-5048T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210003 | ||||||
| chr13:31210096
|
T | C | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.71-4955T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210096 | ||||||
| chr13:31210219
|
A | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.71-4832A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210219 | ||||||
| chr13:31210273
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.71-4778A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210273 | ||||||
| chr13:31210386
|
G | A | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-4665G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210386 | ||||||
| chr13:31210553
|
G | T | 5 | a0001c0001t0005g0206a0001c0001t0005g0207a0003c0004t0004g0205others(2): Show | 5 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-4498G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210553 | ||||||
| chr13:31210701
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-4350G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210701 | ||||||
| chr13:31210798
|
G | A | 1 | a0002c0002t0003g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.71-4253G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210798 | ||||||
| chr13:31210812
|
A | G | 3 | a0001c0001t0004g0044a0001c0001t0004g0061a0002c0002t0008g0060 | 3 | NA18953.hp1 NA18963.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.71-4239A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210812 | ||||||
| chr13:31211026
|
T | C | 2 | a0002c0002t0002g0087a0002c0002t0002g0095 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-4025T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211026 | ||||||
| chr13:31211256
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71-3795A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211256 | ||||||
| chr13:31211267
|
T | C | 177 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.71-3784T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211267 | ||||||
| chr13:31211282
|
C | G | 2 | a0001c0013t0001g0262a0002c0003t0003g0188 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.71-3769C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211282 | ||||||
| chr13:31211310
|
C | T | 44 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(41): Show | 44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3741C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211310 | ||||||
| chr13:31211377
|
C | T | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-3674C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211377 | ||||||
| chr13:31211411
|
C | T | 44 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(41): Show | 44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3640C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211411 | ||||||
| chr13:31211425
|
TC | T | 5 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3625delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211425 | ||||||
| chr13:31211463
|
T | A | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-3588T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211463 | ||||||
| chr13:31211484
|
T | C | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-3567T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211484 | ||||||
| chr13:31211589
|
GT | G | 6 | a0001c0001t0001g0152a0002c0002t0002g0126a0002c0002t0003g0240others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3449delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31211589 | |||||
| chr13:31211739
|
A | G | 264 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.71-3312A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211739 | ||||||
| chr13:31211850
|
C | G | 44 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(41): Show | 44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3201C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211850 | ||||||
| chr13:31211923
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-3128G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211923 | ||||||
| chr13:31212000
|
G | A | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-3051G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212000 | ||||||
| chr13:31212109
|
A | T | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71-2942A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212109 | ||||||
| chr13:31212109
|
AT | A | 6 | a0001c0001t0001g0152a0002c0002t0002g0127a0002c0002t0003g0240others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2928delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212109 | |||||
| chr13:31212155
|
A | G | 3 | a0002c0002t0003g0240a0002c0003t0021g0068a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-2896A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212155 | ||||||
| chr13:31212267
|
C | CT | 13 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0107others(10): Show | 13 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-2759dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | |||||
| chr13:31212267
|
CT | C | 81 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0069others(78): Show | 82 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.71-2759delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | |||||
| chr13:31212267
|
CTTTTTTT others(5): Show |
C | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-2770_71-2759del others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | |||||
| chr13:31212309
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.71-2742C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212309 | ||||||
| chr13:31212516
|
G | A | 6 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2535G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212516 | ||||||
| chr13:31212553
|
G | C | 2 | a0002c0002t0002g0029a0002c0002t0002g0030 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.71-2498G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212553 | ||||||
| chr13:31212648
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-2403G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212648 | ||||||
| chr13:31212704
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-2347G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212704 | ||||||
| chr13:31213018
|
T | TTG | 6 | a0002c0002t0003g0240a0002c0002t0003g0265a0002c0002t0009g0210others(3): Show | 6 | HG01496.hp2 HG02015.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2016_71-2015dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213018 | |||||
| chr13:31213019
|
T | TGTGTGTG others(21): Show |
17 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0005g0001others(14): Show | 18 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-2021_71-1994dup others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213019 | |||||
| chr13:31213042
|
G | A | 13 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(10): Show | 13 | HG01106.hp2 HG01243.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-2009G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213042 | ||||||
| chr13:31213045
|
C | T | 1 | a0002c0008t0002g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.71-2006C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213045 | ||||||
| chr13:31213048
|
G | A | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-2003G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213048 | ||||||
| chr13:31213090
|
C | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-1961C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213090 | ||||||
| chr13:31213221
|
C | G | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-1830C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213221 | ||||||
| chr13:31213416
|
C | T | 3 | a0002c0002t0003g0240a0002c0003t0021g0068a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1635C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213416 | ||||||
| chr13:31213461
|
A | G | 3 | a0002c0002t0003g0240a0002c0003t0021g0068a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1590A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213461 | ||||||
| chr13:31213608
|
A | ACCCCCCC others(3): Show |
1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213608 | |||||
| chr13:31213608
|
A | ACCCCCCC others(13): Show |
1 | a0002c0002t0002g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213608 | |||||
| chr13:31213610
|
C | CCCCCCCA others(8): Show |
1 | a0001c0001t0001g0124 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213610 | |||||
| chr13:31213616
|
A | ACCCCCCA others(4): Show |
1 | a0001c0001t0001g0136 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCA others(6): Show |
1 | a0002c0002t0002g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(13): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(3): Show |
3 | a0001c0001t0001g0118a0001c0001t0004g0119a0001c0001t0004g0120 | 3 | NA18944.hp1 NA18952.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.71-1431_71-1430ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(5): Show |
1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(8): Show |
1 | a0002c0002t0008g0083 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(4): Show |
1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(3): Show |
1 | a0002c0002t0002g0138 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(5): Show |
1 | a0002c0002t0002g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(6): Show |
1 | a0002c0002t0008g0125 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(13): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | ACCCCCCC others(9): Show |
1 | a0002c0002t0002g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | |||||
| chr13:31213616
|
A | C | 7 | a0001c0001t0001g0124a0002c0002t0002g0127a0002c0002t0002g0134others(4): Show | 7 | HG02698.hp2 HG03225.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1435A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213616 | ||||||
| chr13:31213617
|
C | A | 1 | a0002c0002t0002g0167 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.71-1434C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213617 | ||||||
| chr13:31213620
|
C | A | 9 | a0001c0001t0001g0178a0002c0002t0002g0179a0002c0002t0002g0180others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-1431C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213620 | ||||||
| chr13:31213621
|
A | AC | 29 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0080others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-1418dupC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | |||||
| chr13:31213621
|
A | ACC | 79 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(76): Show | 79 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.71-1419_71-1418dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | |||||
| chr13:31213621
|
A | ACCC | 32 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0089others(29): Show | 32 | HG00738.hp1 HG00738.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-1420_71-1418dup others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | |||||
| chr13:31213621
|
A | ACCCCACC others(3): Show |
1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-1426_71-1425ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | |||||
| chr13:31213621
|
A | C | 35 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0118others(32): Show | 35 | HG00609.hp1 HG02027.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.71-1430A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213621 | ||||||
| chr13:31213621
|
ACC | A | 19 | a0001c0001t0001g0242a0001c0001t0005g0254a0002c0002t0001g0252others(16): Show | 20 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.71-1419_71-1418del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | |||||
| chr13:31213622
|
C | A | 2 | a0001c0001t0001g0175a0002c0002t0012g0176 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.71-1429C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213622 | ||||||
| chr13:31213623
|
C | CCCCCCCC others(3): Show |
1 | a0001c0001t0005g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71-1419_71-1418ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213623 | |||||
| chr13:31213623
|
C | CCCCCCCC others(4): Show |
3 | a0001c0001t0005g0200a0001c0001t0005g0206a0001c0001t0006g0197 | 3 | HG00140.hp2 HG00735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213623 | |||||
| chr13:31213624
|
C | CCCCCCCC others(3): Show |
10 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(7): Show | 10 | HG01071.hp2 HG01074.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213624 | |||||
| chr13:31213624
|
C | CCCCCCCC others(4): Show |
2 | a0001c0001t0005g0045a0003c0004t0004g0209 | 2 | HG00609.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213624 | |||||
| chr13:31213642
|
T | C | 3 | a0002c0002t0003g0240a0002c0003t0021g0068a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1409T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213642 | ||||||
| chr13:31213789
|
G | T | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1262G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213789 | ||||||
| chr13:31213867
|
G | T | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-1184G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213867 | ||||||
| chr13:31213966
|
A | C | 1 | a0002c0002t0003g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.71-1085A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213966 | ||||||
| chr13:31214111
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-940C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214111 | ||||||
| chr13:31214198
|
T | G | 167 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.71-853T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214198 | ||||||
| chr13:31214235
|
A | C | 1 | a0002c0002t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-816A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214235 | ||||||
| chr13:31214388
|
A | G | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-663A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214388 | ||||||
| chr13:31214423
|
C | T | 2 | a0001c0001t0001g0103a0002c0002t0008g0096 | 2 | HG02074.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.71-628C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214423 | ||||||
| chr13:31214488
|
C | T | 1 | a0002c0002t0003g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-563C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214488 | ||||||
| chr13:31214516
|
G | C | 5 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-535G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214516 | ||||||
| chr13:31214665
|
G | T | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-386G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214665 | ||||||
| chr13:31214754
|
T | A | 1 | a0001c0001t0004g0047 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.71-297T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214754 | ||||||
| chr13:31214811
|
T | G | 1 | a0002c0002t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71-240T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214811 | ||||||
| chr13:31214957
|
A | C | 1 | a0001c0001t0005g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71-94A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214957 | ||||||
| chr13:31215032
|
CT | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
splice_region_variant&intron_variant | LOW | c.71-5delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31215032 | |||||
| chr13:31215259
|
A | G | 1 | a0001c0001t0005g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120+159A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215259 | ||||||
| chr13:31215339
|
G | A | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.120+239G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215339 | ||||||
| chr13:31215433
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.120+333C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215433 | ||||||
| chr13:31215600
|
G | T | 2 | a0001c0001t0001g0043a0006c0012t0004g0059 | 2 | NA18984.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.120+500G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215600 | ||||||
| chr13:31215603
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.120+503G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215603 | ||||||
| chr13:31215639
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+539C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215639 | ||||||
| chr13:31215699
|
C | T | 26 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(23): Show | 27 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.120+599C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215699 | ||||||
| chr13:31215756
|
T | C | 4 | a0002c0002t0003g0265a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 HG02922.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+656T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215756 | ||||||
| chr13:31215794
|
A | G | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.120+694A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215794 | ||||||
| chr13:31215796
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120+696C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215796 | ||||||
| chr13:31215856
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.120+756G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215856 | ||||||
| chr13:31215916
|
C | T | 29 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(26): Show | 30 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.120+816C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215916 | ||||||
| chr13:31216147
|
C | CT | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.120+1050dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216147 | |||||
| chr13:31216237
|
G | A | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.120+1137G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216237 | ||||||
| chr13:31216384
|
TTTTTTCT others(51): Show |
T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+1337_120+1394d others(60): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216384 | |||||
| chr13:31216483
|
T | TG | 6 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0003g0265others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+1384dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216483 | |||||
| chr13:31216605
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+1505C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216605 | ||||||
| chr13:31216639
|
C | G | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120+1539C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216639 | ||||||
| chr13:31216786
|
C | A | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.120+1686C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216786 | ||||||
| chr13:31216875
|
A | T | 7 | a0002c0002t0003g0009a0002c0002t0003g0031a0002c0002t0003g0033others(4): Show | 7 | HG01175.hp1 HG01243.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+1775A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216875 | ||||||
| chr13:31217221
|
T | C | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.120+2121T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217221 | ||||||
| chr13:31217279
|
A | G | 99 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.120+2179A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217279 | ||||||
| chr13:31217389
|
G | C | 51 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.120+2289G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217389 | ||||||
| chr13:31217518
|
A | G | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2418A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217518 | ||||||
| chr13:31217519
|
C | A | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2419C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217519 | ||||||
| chr13:31217548
|
T | C | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2448T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217548 | ||||||
| chr13:31217626
|
A | G | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2526A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217626 | ||||||
| chr13:31217664
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+2564C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217664 | ||||||
| chr13:31217806
|
A | C | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.120+2706A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217806 | ||||||
| chr13:31217822
|
G | T | 2 | a0001c0001t0004g0037a0001c0001t0004g0058 | 2 | HG00673.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.120+2722G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217822 | ||||||
| chr13:31217830
|
T | C | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+2730T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217830 | ||||||
| chr13:31217972
|
T | A | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2872T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217972 | ||||||
| chr13:31217978
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+2878G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217978 | ||||||
| chr13:31218186
|
A | G | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+3086A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218186 | ||||||
| chr13:31218187
|
C | CT | 6 | a0001c0001t0001g0086a0002c0002t0003g0094a0002c0002t0003g0246others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+3106dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218187 | |||||
| chr13:31218187
|
CT | C | 72 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(69): Show | 73 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.120+3106delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218187 | |||||
| chr13:31218238
|
A | G | 260 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.120+3138A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218238 | ||||||
| chr13:31218239
|
G | T | 1 | a0002c0002t0009g0013 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.120+3139G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218239 | ||||||
| chr13:31218617
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.120+3517A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218617 | ||||||
| chr13:31218751
|
G | A | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.120+3651G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218751 | ||||||
| chr13:31218811
|
G | A | 1 | a0002c0002t0004g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120+3711G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218811 | ||||||
| chr13:31218930
|
C | CT | 137 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.120+3843dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218930 | |||||
| chr13:31218990
|
A | G | 1 | a0002c0002t0002g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.120+3890A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218990 | ||||||
| chr13:31219154
|
G | A | 1 | a0002c0002t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121-3798G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219154 | ||||||
| chr13:31219155
|
T | C | 3 | a0001c0001t0001g0175a0002c0002t0012g0174a0002c0002t0012g0176 | 3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.121-3797T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219155 | ||||||
| chr13:31219229
|
C | G | 3 | a0002c0002t0003g0077a0002c0002t0003g0078a0002c0002t0003g0260 | 3 | HG03834.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.121-3723C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219229 | ||||||
| chr13:31219324
|
A | C | 1 | a0001c0001t0004g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121-3628A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219324 | ||||||
| chr13:31219434
|
T | C | 26 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(23): Show | 27 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.121-3518T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219434 | ||||||
| chr13:31219435
|
T | A | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-3517T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219435 | ||||||
| chr13:31219621
|
T | C | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.121-3331T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219621 | ||||||
| chr13:31219752
|
A | G | 5 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-3200A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219752 | ||||||
| chr13:31219813
|
A | C | 53 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.121-3139A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219813 | ||||||
| chr13:31219885
|
G | C | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-3067G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219885 | ||||||
| chr13:31220465
|
T | G | 1 | a0001c0001t0004g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121-2487T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220465 | ||||||
| chr13:31220488
|
T | C | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.121-2464T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220488 | ||||||
| chr13:31220594
|
T | G | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.121-2358T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220594 | ||||||
| chr13:31220658
|
A | G | 1 | a0001c0001t0007g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-2294A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220658 | ||||||
| chr13:31220843
|
T | C | 3 | a0002c0002t0002g0127a0002c0002t0002g0137a0002c0002t0002g0140 | 3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.121-2109T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220843 | ||||||
| chr13:31220899
|
A | T | 1 | a0002c0002t0002g0167 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.121-2053A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220899 | ||||||
| chr13:31220940
|
T | C | 1 | a0001c0001t0004g0061 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.121-2012T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220940 | ||||||
| chr13:31220967
|
A | G | 9 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0003g0265others(6): Show | 9 | HG02015.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-1985A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220967 | ||||||
| chr13:31221053
|
T | C | 2 | a0001c0001t0006g0054a0001c0001t0006g0169 | 2 | NA18947.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.121-1899T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221053 | ||||||
| chr13:31221291
|
T | C | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.121-1661T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221291 | ||||||
| chr13:31221409
|
G | A | 51 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-1543G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221409 | ||||||
| chr13:31221570
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.121-1382C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221570 | ||||||
| chr13:31221640
|
C | T | 1 | a0001c0001t0007g0028 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.121-1312C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221640 | ||||||
| chr13:31221641
|
C | T | 1 | a0001c0001t0005g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121-1311C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221641 | ||||||
| chr13:31221818
|
A | G | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.121-1134A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221818 | ||||||
| chr13:31221823
|
G | A | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.121-1129G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221823 | ||||||
| chr13:31221921
|
T | C | 1 | a0002c0002t0003g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.121-1031T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221921 | ||||||
| chr13:31221973
|
C | T | 1 | a0001c0001t0010g0110 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.121-979C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221973 | ||||||
| chr13:31222043
|
C | A | 21 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(18): Show | 22 | HG01123.hp1 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.121-909C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222043 | ||||||
| chr13:31222043
|
C | G | 5 | a0002c0002t0003g0012a0002c0002t0003g0079a0002c0002t0003g0243others(2): Show | 5 | HG01255.hp1 HG01358.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-909C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222043 | ||||||
| chr13:31222074
|
A | AT | 8 | a0001c0001t0001g0069a0002c0002t0003g0012a0002c0002t0003g0079others(5): Show | 8 | HG01255.hp1 HG01358.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-856dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | |||||
| chr13:31222074
|
AT | A | 165 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0043others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.121-856delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | |||||
| chr13:31222074
|
ATT | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0108others(2): Show | 5 | HG00140.hp1 HG01169.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-857_121-856del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | |||||
| chr13:31222169
|
C | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121-783C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222169 | ||||||
| chr13:31222266
|
G | A | 260 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.121-686G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222266 | ||||||
| chr13:31222341
|
G | T | 51 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-611G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222341 | ||||||
| chr13:31222426
|
T | G | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.121-526T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222426 | ||||||
| chr13:31222503
|
A | C | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-449A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222503 | ||||||
| chr13:31222605
|
A | G | 166 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.121-347A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222605 | ||||||
| chr13:31222832
|
G | C | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.121-120G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222832 | ||||||
| chr13:31222869
|
A | G | 78 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(75): Show | 79 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.121-83A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222869 | ||||||
| chr13:31222871
|
G | A | 1 | a0002c0002t0002g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.121-81G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222871 | ||||||
| chr13:31223294
|
G | A | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.160+303G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223294 | ||||||
| chr13:31223318
|
C | T | 51 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.160+327C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223318 | ||||||
| chr13:31223504
|
T | C | 189 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.160+513T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223504 | ||||||
| chr13:31223758
|
G | T | 5 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+767G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223758 | ||||||
| chr13:31223842
|
G | A | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+851G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223842 | ||||||
| chr13:31223938
|
T | C | 49 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0242others(46): Show | 51 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.160+947T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223938 | ||||||
| chr13:31223939
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+948C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223939 | ||||||
| chr13:31224071
|
A | G | 1 | a0001c0001t0007g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+1080A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224071 | ||||||
| chr13:31224083
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+1092C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224083 | ||||||
| chr13:31224084
|
G | A | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.160+1093G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224084 | ||||||
| chr13:31224089
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+1098C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224089 | ||||||
| chr13:31224274
|
A | G | 1 | a0002c0002t0002g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+1283A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224274 | ||||||
| chr13:31224290
|
C | T | 1 | a0002c0002t0003g0244 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.160+1299C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224290 | ||||||
| chr13:31224313
|
C | T | 1 | a0002c0002t0013g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160+1322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224313 | ||||||
| chr13:31224355
|
T | G | 3 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0008t0002g0063 | 3 | HG01891.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160+1364T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224355 | ||||||
| chr13:31224713
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+1722G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224713 | ||||||
| chr13:31224720
|
G | A | 1 | a0002c0002t0002g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160+1729G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224720 | ||||||
| chr13:31224770
|
T | G | 1 | a0002c0002t0003g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+1779T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224770 | ||||||
| chr13:31224816
|
G | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+1825G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224816 | ||||||
| chr13:31224928
|
T | C | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.160+1937T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224928 | ||||||
| chr13:31225091
|
C | T | 2 | a0001c0001t0001g0043a0006c0012t0004g0059 | 2 | NA18984.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+2100C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225091 | ||||||
| chr13:31225161
|
G | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+2170G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225161 | ||||||
| chr13:31225509
|
G | A | 30 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(27): Show | 31 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.160+2518G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225509 | ||||||
| chr13:31225582
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+2591C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225582 | ||||||
| chr13:31225595
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+2604G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225595 | ||||||
| chr13:31225653
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160+2662C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225653 | ||||||
| chr13:31225694
|
G | A | 2 | a0001c0001t0005g0099a0001c0001t0005g0104 | 2 | NA18612.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.160+2703G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225694 | ||||||
| chr13:31225804
|
A | G | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.160+2813A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225804 | ||||||
| chr13:31225842
|
C | G | 96 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.160+2851C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225842 | ||||||
| chr13:31226032
|
A | G | 2 | a0002c0002t0011g0005a0002c0002t0011g0006 | 2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.160+3041A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226032 | ||||||
| chr13:31226072
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+3081C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226072 | ||||||
| chr13:31226101
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.161-3084A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226101 | ||||||
| chr13:31226115
|
A | G | 137 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.161-3070A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226115 | ||||||
| chr13:31226120
|
C | A | 26 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(23): Show | 27 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.161-3065C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226120 | ||||||
| chr13:31226147
|
G | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-3038G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226147 | ||||||
| chr13:31226202
|
T | C | 3 | a0002c0002t0003g0077a0002c0002t0003g0078a0002c0002t0003g0260 | 3 | HG03834.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.161-2983T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226202 | ||||||
| chr13:31226205
|
C | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-2980C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226205 | ||||||
| chr13:31226237
|
G | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-2948G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226237 | ||||||
| chr13:31226348
|
A | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.161-2837A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226348 | ||||||
| chr13:31226488
|
A | G | 14 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0159others(11): Show | 14 | HG00558.hp1 HG01943.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-2697A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226488 | ||||||
| chr13:31226580
|
C | T | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.161-2605C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226580 | ||||||
| chr13:31226596
|
T | A | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.161-2589T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226596 | ||||||
| chr13:31226608
|
A | AT | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-2568dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31226608 | |||||
| chr13:31226878
|
A | C | 2 | a0002c0002t0012g0174a0002c0002t0012g0176 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.161-2307A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226878 | ||||||
| chr13:31226947
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.161-2238A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226947 | ||||||
| chr13:31226954
|
T | C | 137 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.161-2231T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226954 | ||||||
| chr13:31227329
|
TA | T | 7 | a0001c0001t0001g0069a0001c0001t0004g0041a0002c0002t0003g0240others(4): Show | 7 | HG01071.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-1846delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31227329 | |||||
| chr13:31227405
|
G | A | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.161-1780G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227405 | ||||||
| chr13:31227431
|
T | C | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-1754T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227431 | ||||||
| chr13:31227771
|
T | C | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-1414T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227771 | ||||||
| chr13:31227811
|
G | A | 4 | a0002c0002t0003g0238a0002c0002t0003g0245a0002c0002t0003g0247others(1): Show | 4 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1374G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227811 | ||||||
| chr13:31227872
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161-1313G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227872 | ||||||
| chr13:31227894
|
G | C | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.161-1291G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227894 | ||||||
| chr13:31227911
|
C | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-1274C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227911 | ||||||
| chr13:31227990
|
C | T | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-1195C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227990 | ||||||
| chr13:31228090
|
G | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.161-1095G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228090 | ||||||
| chr13:31228156
|
G | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-1029G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228156 | ||||||
| chr13:31228219
|
C | CG | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.161-965dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31228219 | |||||
| chr13:31228265
|
T | G | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.161-920T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228265 | ||||||
| chr13:31228275
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-910A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228275 | ||||||
| chr13:31228402
|
A | G | 186 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.161-783A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228402 | ||||||
| chr13:31228494
|
A | G | 49 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0242others(46): Show | 51 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.161-691A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228494 | ||||||
| chr13:31228563
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-622G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228563 | ||||||
| chr13:31228707
|
A | G | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-478A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228707 | ||||||
| chr13:31228733
|
T | C | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.161-452T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228733 | ||||||
| chr13:31228786
|
A | G | 1 | a0002c0003t0002g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.161-399A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228786 | ||||||
| chr13:31228856
|
C | G | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.161-329C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228856 | ||||||
| chr13:31228879
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-306C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228879 | ||||||
| chr13:31229021
|
AAG | A | 3 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0007t0023g0004 | 3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-158_161-157del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31229021 | |||||
| chr13:31229472
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.270+178G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229472 | ||||||
| chr13:31229521
|
G | A | 1 | a0002c0002t0003g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+227G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229521 | ||||||
| chr13:31229635
|
A | T | 1 | a0002c0002t0004g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.270+341A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229635 | ||||||
| chr13:31229762
|
G | A | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.270+468G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229762 | ||||||
| chr13:31229815
|
T | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.270+521T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229815 | ||||||
| chr13:31229817
|
T | G | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.270+523T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229817 | ||||||
| chr13:31229819
|
T | G | 5 | a0001c0001t0001g0069a0002c0002t0003g0240a0002c0002t0008g0060others(2): Show | 5 | HG01496.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+525T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229819 | ||||||
| chr13:31229820
|
TG | T | 4 | a0001c0001t0004g0173a0002c0002t0002g0235a0004c0005t0001g0072others(1): Show | 4 | HG00741.hp2 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+527delG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229820 | ||||||
| chr13:31229821
|
G | T | 121 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.270+527G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229821 | ||||||
| chr13:31229823
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.270+529G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229823 | ||||||
| chr13:31229839
|
A | G | 1 | a0001c0001t0004g0061 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.270+545A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229839 | ||||||
| chr13:31229844
|
A | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0102a0002c0002t0003g0240others(1): Show | 4 | HG01496.hp2 HG02148.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+550A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229844 | ||||||
| chr13:31229904
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.270+610G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229904 | ||||||
| chr13:31229953
|
T | C | 2 | a0001c0001t0004g0218a0002c0002t0003g0241 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.270+659T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229953 | ||||||
| chr13:31230039
|
C | T | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(4): Show | 7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+745C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230039 | ||||||
| chr13:31230156
|
G | A | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+862G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230156 | ||||||
| chr13:31230303
|
A | G | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.270+1009A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230303 | ||||||
| chr13:31230348
|
G | A | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.270+1054G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230348 | ||||||
| chr13:31230428
|
T | C | 2 | a0001c0001t0010g0003a0001c0001t0010g0109 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.270+1134T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230428 | ||||||
| chr13:31230537
|
T | G | 264 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.270+1243T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230537 | ||||||
| chr13:31230613
|
GCTCTGCT others(65): Show |
G | 1 | a0002c0002t0009g0212 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.270+1320_270+1391d others(74): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230613 | ||||||
| chr13:31230721
|
C | T | 1 | a0002c0002t0009g0212 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.270+1427C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230721 | ||||||
| chr13:31230786
|
G | A | 1 | a0002c0002t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.270+1492G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230786 | ||||||
| chr13:31230855
|
A | G | 49 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0242others(46): Show | 51 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.270+1561A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230855 | ||||||
| chr13:31231008
|
A | G | 1 | a0002c0002t0003g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.270+1714A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231008 | ||||||
| chr13:31231482
|
C | T | 5 | a0001c0001t0001g0178a0002c0002t0002g0179a0002c0002t0004g0172others(2): Show | 5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+2188C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231482 | ||||||
| chr13:31231679
|
C | T | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+2385C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231679 | ||||||
| chr13:31231710
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.270+2416A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231710 | ||||||
| chr13:31231984
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+2690T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231984 | ||||||
| chr13:31232158
|
T | C | 5 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+2864T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232158 | ||||||
| chr13:31232279
|
A | C | 5 | a0001c0001t0001g0178a0002c0002t0002g0179a0002c0002t0004g0172others(2): Show | 5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+2985A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232279 | ||||||
| chr13:31232420
|
TAGAG | T | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3133_270+3136d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31232420 | |||||
| chr13:31232430
|
G | C | 1 | a0002c0002t0003g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.270+3136G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232430 | ||||||
| chr13:31232439
|
C | T | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3145C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232439 | ||||||
| chr13:31232486
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+3192C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232486 | ||||||
| chr13:31232501
|
G | A | 1 | a0001c0001t0004g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+3207G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232501 | ||||||
| chr13:31232537
|
C | G | 1 | a0002c0002t0002g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.270+3243C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232537 | ||||||
| chr13:31232621
|
G | A | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.270+3327G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232621 | ||||||
| chr13:31232747
|
G | A | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3453G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232747 | ||||||
| chr13:31232835
|
C | T | 53 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.270+3541C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232835 | ||||||
| chr13:31232986
|
C | T | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.270+3692C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232986 | ||||||
| chr13:31232994
|
C | T | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+3700C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232994 | ||||||
| chr13:31233146
|
T | A | 2 | a0002c0002t0003g0240a0002c0007t0023g0004 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.270+3852T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233146 | ||||||
| chr13:31233246
|
G | A | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.270+3952G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233246 | ||||||
| chr13:31233594
|
G | A | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4300G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233594 | ||||||
| chr13:31233659
|
C | G | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4365C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233659 | ||||||
| chr13:31233900
|
A | G | 49 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0242others(46): Show | 51 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.270+4606A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233900 | ||||||
| chr13:31233906
|
C | T | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4612C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233906 | ||||||
| chr13:31234007
|
C | CT | 135 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4725dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31234007 | |||||
| chr13:31234007
|
CT | C | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+4725delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31234007 | |||||
| chr13:31234103
|
C | T | 4 | a0001c0001t0010g0003a0001c0001t0010g0109a0001c0001t0010g0110others(1): Show | 4 | HG00558.hp2 HG00673.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+4809C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234103 | ||||||
| chr13:31234143
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.270+4849G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234143 | ||||||
| chr13:31234163
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.270+4869A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234163 | ||||||
| chr13:31234166
|
C | T | 3 | a0002c0002t0009g0210a0002c0002t0009g0211a0002c0002t0009g0212 | 3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.270+4872C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234166 | ||||||
| chr13:31234176
|
C | T | 1 | a0002c0002t0003g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270+4882C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234176 | ||||||
| chr13:31234248
|
C | T | 51 | a0001c0001t0001g0069a0001c0001t0001g0192a0001c0001t0001g0193others(48): Show | 53 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.270+4954C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234248 | ||||||
| chr13:31234277
|
C | T | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+4983C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234277 | ||||||
| chr13:31234457
|
T | C | 1 | a0002c0002t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.270+5163T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234457 | ||||||
| chr13:31234489
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.270+5195C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234489 | ||||||
| chr13:31234672
|
G | A | 1 | a0002c0002t0011g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.270+5378G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234672 | ||||||
| chr13:31234748
|
A | T | 2 | a0001c0001t0004g0218a0002c0002t0003g0241 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.270+5454A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234748 | ||||||
| chr13:31234914
|
G | A | 5 | a0002c0002t0002g0266a0002c0002t0003g0229a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+5620G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234914 | ||||||
| chr13:31235038
|
C | T | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+5744C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235038 | ||||||
| chr13:31235202
|
A | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.270+5908A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235202 | ||||||
| chr13:31235236
|
A | G | 1 | a0002c0002t0020g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.270+5942A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235236 | ||||||
| chr13:31235300
|
G | A | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+6006G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235300 | ||||||
| chr13:31235444
|
G | A | 58 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(55): Show | 58 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.270+6150G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235444 | ||||||
| chr13:31235564
|
CAG | C | 39 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(36): Show | 39 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+6276_270+6277d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31235564 | |||||
| chr13:31235587
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.270+6293C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235587 | ||||||
| chr13:31235602
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.270+6308T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235602 | ||||||
| chr13:31235612
|
G | A | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+6318G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235612 | ||||||
| chr13:31235723
|
A | G | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+6429A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235723 | ||||||
| chr13:31235751
|
G | A | 1 | a0002c0002t0002g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.270+6457G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235751 | ||||||
| chr13:31235773
|
C | T | 1 | a0001c0001t0005g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.270+6479C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235773 | ||||||
| chr13:31235803
|
T | C | 205 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.270+6509T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235803 | ||||||
| chr13:31235831
|
A | C | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.270+6537A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235831 | ||||||
| chr13:31235962
|
G | T | 1 | a0002c0002t0003g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.270+6668G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235962 | ||||||
| chr13:31236844
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | NA18950.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.270+7550G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236844 | ||||||
| chr13:31236937
|
G | A | 10 | a0001c0001t0007g0016a0002c0002t0003g0009a0002c0002t0003g0025others(7): Show | 10 | HG00738.hp1 HG01175.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+7643G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236937 | ||||||
| chr13:31236982
|
C | T | 136 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.270+7688C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236982 | ||||||
| chr13:31237042
|
C | T | 1 | a0002c0002t0012g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.270+7748C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237042 | ||||||
| chr13:31237125
|
C | CA | 140 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.270+7844dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237125 | |||||
| chr13:31237350
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.270+8056G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237350 | ||||||
| chr13:31237353
|
G | GT | 185 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.270+8077dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237353 | |||||
| chr13:31237353
|
G | GTT | 66 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0098others(63): Show | 68 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.270+8076_270+8077d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237353 | |||||
| chr13:31237551
|
C | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+8257C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237551 | ||||||
| chr13:31237613
|
C | T | 1 | a0004c0005t0001g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+8319C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237613 | ||||||
| chr13:31237652
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+8358G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237652 | ||||||
| chr13:31237678
|
G | A | 63 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(60): Show | 63 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.270+8384G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237678 | ||||||
| chr13:31237682
|
A | G | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+8388A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237682 | ||||||
| chr13:31237717
|
G | A | 1 | a0002c0002t0003g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+8423G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237717 | ||||||
| chr13:31237828
|
A | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0006g0052others(2): Show | 5 | HG00558.hp1 NA18968.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+8534A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237828 | ||||||
| chr13:31237902
|
G | C | 3 | a0001c0001t0001g0175a0002c0002t0012g0174a0002c0002t0012g0176 | 3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.270+8608G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237902 | ||||||
| chr13:31237961
|
G | A | 1 | a0002c0002t0003g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.270+8667G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237961 | ||||||
| chr13:31238110
|
T | A | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+8816T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238110 | ||||||
| chr13:31238237
|
G | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-8786G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238237 | ||||||
| chr13:31238441
|
T | C | 1 | a0002c0002t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.271-8582T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238441 | ||||||
| chr13:31238523
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.271-8500C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238523 | ||||||
| chr13:31238575
|
T | G | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-8448T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238575 | ||||||
| chr13:31238677
|
C | T | 17 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0005g0001others(14): Show | 18 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-8346C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238677 | ||||||
| chr13:31238752
|
G | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0092a0001c0001t0001g0100others(6): Show | 9 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-8271G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238752 | ||||||
| chr13:31238888
|
C | T | 1 | a0002c0002t0002g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271-8135C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238888 | ||||||
| chr13:31238895
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-8128G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238895 | ||||||
| chr13:31238977
|
C | T | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-8046C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238977 | ||||||
| chr13:31238978
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0136 | 2 | NA18978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.271-8045G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238978 | ||||||
| chr13:31239085
|
G | A | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.271-7938G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239085 | ||||||
| chr13:31239396
|
GAGAC | G | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-7619_271-7616d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239396 | |||||
| chr13:31239636
|
A | G | 1 | a0001c0013t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-7387A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239636 | ||||||
| chr13:31239684
|
C | CT | 14 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(11): Show | 14 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-7324dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | |||||
| chr13:31239684
|
C | CTT | 20 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(17): Show | 21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-7325_271-7324d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | |||||
| chr13:31239684
|
CT | C | 55 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(52): Show | 55 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.271-7324delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | |||||
| chr13:31239730
|
C | G | 260 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.271-7293C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239730 | ||||||
| chr13:31239734
|
T | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.271-7289T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239734 | ||||||
| chr13:31239853
|
G | C | 218 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.271-7170G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239853 | ||||||
| chr13:31240181
|
T | C | 25 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(22): Show | 26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.271-6842T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240181 | ||||||
| chr13:31240234
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.271-6789C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240234 | ||||||
| chr13:31240285
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-6738A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240285 | ||||||
| chr13:31240327
|
G | A | 25 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(22): Show | 26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.271-6696G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240327 | ||||||
| chr13:31240463
|
T | G | 117 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(114): Show | 119 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.271-6560T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240463 | ||||||
| chr13:31240467
|
G | GT | 27 | a0001c0001t0001g0102a0001c0001t0001g0189a0001c0001t0001g0242others(24): Show | 28 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.271-6546dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240467 | |||||
| chr13:31240477
|
T | TTC | 62 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0070others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.271-6546_271-6545i others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240477 | ||||||
| chr13:31240478
|
C | CT | 94 | a0001c0001t0001g0022a0001c0001t0001g0086a0001c0001t0001g0117others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-6532dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240478 | |||||
| chr13:31240478
|
C | CTT | 14 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0175others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-6533_271-6532d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240478 | |||||
| chr13:31240478
|
C | T | 62 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0070others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.271-6545C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240478 | ||||||
| chr13:31240494
|
A | G | 52 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(49): Show | 52 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.271-6529A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240494 | ||||||
| chr13:31240522
|
A | G | 1 | a0001c0013t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-6501A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240522 | ||||||
| chr13:31240586
|
C | T | 25 | a0001c0001t0001g0242a0001c0001t0004g0218a0001c0001t0005g0254others(22): Show | 26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.271-6437C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240586 | ||||||
| chr13:31240780
|
T | C | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-6243T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240780 | ||||||
| chr13:31241194
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-5829C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241194 | ||||||
| chr13:31241224
|
C | G | 1 | a0002c0002t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271-5799C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241224 | ||||||
| chr13:31241252
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-5771G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241252 | ||||||
| chr13:31241281
|
C | T | 1 | a0002c0002t0002g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.271-5742C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241281 | ||||||
| chr13:31241296
|
G | T | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271-5727G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241296 | ||||||
| chr13:31241532
|
A | G | 11 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(8): Show | 11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-5491A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241532 | ||||||
| chr13:31241580
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0136 | 2 | NA18978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.271-5443T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241580 | ||||||
| chr13:31241665
|
A | C | 15 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0002g0179others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-5358A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241665 | ||||||
| chr13:31241741
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.271-5282T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241741 | ||||||
| chr13:31241743
|
G | A | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-5280G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241743 | ||||||
| chr13:31241770
|
C | T | 2 | a0002c0002t0013g0008a0002c0002t0013g0191 | 2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.271-5253C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241770 | ||||||
| chr13:31241820
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-5203G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241820 | ||||||
| chr13:31241879
|
G | A | 134 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.271-5144G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241879 | ||||||
| chr13:31241998
|
A | C | 2 | a0002c0002t0002g0195a0002c0002t0002g0196 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-5025A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241998 | ||||||
| chr13:31242164
|
TTC | T | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4853_271-4852d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31242164 | |||||
| chr13:31242192
|
G | A | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4831G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242192 | ||||||
| chr13:31242285
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4738T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242285 | ||||||
| chr13:31242371
|
G | T | 1 | a0001c0001t0004g0053 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.271-4652G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242371 | ||||||
| chr13:31242387
|
A | G | 54 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0242others(51): Show | 56 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.271-4636A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242387 | ||||||
| chr13:31242423
|
G | A | 1 | a0001c0001t0015g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.271-4600G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242423 | ||||||
| chr13:31242429
|
T | G | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4594T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242429 | ||||||
| chr13:31242473
|
C | T | 55 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(52): Show | 55 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.271-4550C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242473 | ||||||
| chr13:31242632
|
A | C | 95 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-4391A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242632 | ||||||
| chr13:31242754
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4269C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242754 | ||||||
| chr13:31242787
|
A | G | 1 | a0002c0002t0004g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.271-4236A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242787 | ||||||
| chr13:31242811
|
T | C | 19 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(16): Show | 20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4212T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242811 | ||||||
| chr13:31243026
|
C | T | 3 | a0001c0001t0004g0038a0001c0001t0004g0039a0001c0001t0004g0040 | 3 | NA18953.hp2 NA18954.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.271-3997C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243026 | ||||||
| chr13:31243031
|
G | A | 2 | a0001c0001t0007g0028a0001c0001t0007g0112 | 2 | HG01175.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.271-3992G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243031 | ||||||
| chr13:31243108
|
A | T | 57 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0055others(54): Show | 57 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.271-3915A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243108 | ||||||
| chr13:31243320
|
C | A | 2 | a0001c0013t0001g0262a0002c0003t0021g0068 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-3703C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243320 | ||||||
| chr13:31243560
|
A | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3463A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243560 | ||||||
| chr13:31243765
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3258G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243765 | ||||||
| chr13:31244053
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2970C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244053 | ||||||
| chr13:31244219
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2804C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244219 | ||||||
| chr13:31244616
|
G | A | 1 | a0001c0001t0005g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.271-2407G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244616 | ||||||
| chr13:31244747
|
A | G | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.271-2276A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244747 | ||||||
| chr13:31244847
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-2176G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244847 | ||||||
| chr13:31244904
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271-2119T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244904 | ||||||
| chr13:31244963
|
ATGT | A | 79 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(76): Show | 81 | HG00140.hp2 HG00609.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.271-2055_271-2053d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31244963 | |||||
| chr13:31245049
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.271-1974A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245049 | ||||||
| chr13:31245188
|
T | C | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.271-1835T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245188 | ||||||
| chr13:31245230
|
T | C | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-1793T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245230 | ||||||
| chr13:31245247
|
A | C | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.271-1776A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245247 | ||||||
| chr13:31245254
|
C | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.271-1769C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245254 | ||||||
| chr13:31245306
|
T | TTA | 5 | a0001c0001t0005g0254a0002c0002t0003g0238a0002c0002t0003g0245others(2): Show | 5 | HG01358.hp1 HG01516.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1707_271-1706d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31245306 | |||||
| chr13:31245403
|
T | A | 1 | a0002c0002t0009g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.271-1620T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245403 | ||||||
| chr13:31245486
|
G | A | 2 | a0001c0013t0001g0262a0002c0003t0021g0068 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-1537G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245486 | ||||||
| chr13:31245721
|
A | G | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.271-1302A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245721 | ||||||
| chr13:31245814
|
C | A | 63 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(60): Show | 64 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-1209C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245814 | ||||||
| chr13:31245859
|
A | G | 59 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(56): Show | 60 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.271-1164A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245859 | ||||||
| chr13:31246015
|
T | G | 20 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(17): Show | 21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-1008T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246015 | ||||||
| chr13:31246234
|
A | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-789A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246234 | ||||||
| chr13:31246306
|
A | G | 6 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0263others(3): Show | 6 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-717A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246306 | ||||||
| chr13:31246533
|
AAAAGT | A | 138 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.271-482_271-478del others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246533 | |||||
| chr13:31246667
|
C | CT | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-355dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246667 | |||||
| chr13:31246726
|
G | A | 4 | a0001c0001t0001g0178a0002c0002t0004g0172a0002c0002t0004g0182others(1): Show | 4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-297G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246726 | ||||||
| chr13:31246792
|
A | G | 1 | a0001c0001t0004g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.271-231A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246792 | ||||||
| chr13:31246814
|
A | G | 9 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0004g0172others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-209A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246814 | ||||||
| chr13:31246881
|
C | G | 2 | a0001c0013t0001g0262a0002c0003t0021g0068 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-142C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246881 | ||||||
| chr13:31246937
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-86T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246937 | ||||||
| chr13:31246946
|
C | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-77C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246946 | ||||||
| chr13:31246951
|
C | CT | 129 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.271-57dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | |||||
| chr13:31246951
|
C | CTT | 5 | a0001c0001t0001g0178a0001c0001t0001g0223a0002c0002t0004g0172others(2): Show | 5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-58_271-57dupTT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | |||||
| chr13:31246951
|
C | G | 2 | a0002c0002t0009g0210a0002c0002t0009g0212 | 2 | NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.271-72C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246951 | ||||||
| chr13:31246951
|
CT | C | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.271-57delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | |||||
| chr13:31246956
|
T | C | 61 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(58): Show | 62 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(59): Show |
intron_variant | MODIFIER | c.271-67T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246956 | ||||||
| chr13:31246985
|
C | T | 2 | a0001c0013t0001g0262a0002c0003t0021g0068 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-38C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246985 | ||||||
| chr13:31247011
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.271-12T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31247011 | ||||||
| chr13:31247015
|
T | C | 1 | a0002c0010t0003g0010 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.271-8T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31247015 | ||||||
| chr13:31247103
|
C | T | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.347+4C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247103 | ||||||
| chr13:31247119
|
C | G | 54 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(51): Show | 55 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.347+20C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247119 | ||||||
| chr13:31247194
|
A | G | 20 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(17): Show | 21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.347+95A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247194 | ||||||
| chr13:31247289
|
C | CT | 18 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0005g0001others(15): Show | 19 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.347+199dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr13 | 31247289 | |||||
| chr13:31247313
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.347+214G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247313 | ||||||
| chr13:31247332
|
A | G | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.347+233A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247332 | ||||||
| chr13:31247368
|
A | G | 135 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.347+269A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247368 | ||||||
| chr13:31247442
|
T | A | 255 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.347+343T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247442 | ||||||
| chr13:31248100
|
A | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+134A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248100 | ||||||
| chr13:31248170
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.459+204C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248170 | ||||||
| chr13:31248326
|
A | T | 63 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(60): Show | 64 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.459+360A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248326 | ||||||
| chr13:31248404
|
T | C | 1 | a0002c0002t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+438T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248404 | ||||||
| chr13:31248464
|
G | C | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.459+498G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248464 | ||||||
| chr13:31248500
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.459+534A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248500 | ||||||
| chr13:31248530
|
C | G | 189 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.459+564C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248530 | ||||||
| chr13:31248645
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+679G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248645 | ||||||
| chr13:31248647
|
G | A | 2 | a0001c0001t0004g0173a0002c0002t0002g0235 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.459+681G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248647 | ||||||
| chr13:31248886
|
G | A | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+920G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248886 | ||||||
| chr13:31249063
|
G | T | 6 | a0002c0002t0001g0252a0002c0002t0003g0094a0002c0002t0003g0246others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+1097G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249063 | ||||||
| chr13:31249100
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+1134T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249100 | ||||||
| chr13:31249102
|
A | G | 62 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0070others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.459+1136A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249102 | ||||||
| chr13:31249418
|
CTT | C | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+1454_459+1455d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31249418 | |||||
| chr13:31249452
|
G | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+1486G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249452 | ||||||
| chr13:31249798
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+1832G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249798 | ||||||
| chr13:31249855
|
A | G | 24 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(21): Show | 25 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+1889A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249855 | ||||||
| chr13:31249918
|
T | A | 3 | a0001c0001t0001g0055a0001c0001t0006g0052a0001c0001t0022g0050 | 3 | NA18968.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.459+1952T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249918 | ||||||
| chr13:31249919
|
G | A | 1 | a0001c0001t0004g0044 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.459+1953G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249919 | ||||||
| chr13:31249933
|
G | A | 38 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+1967G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249933 | ||||||
| chr13:31250237
|
A | G | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.459+2271A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250237 | ||||||
| chr13:31250247
|
C | T | 1 | a0002c0002t0003g0244 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.459+2281C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250247 | ||||||
| chr13:31250278
|
A | G | 1 | a0001c0001t0004g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.459+2312A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250278 | ||||||
| chr13:31250294
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+2328C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250294 | ||||||
| chr13:31250391
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.459+2425C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250391 | ||||||
| chr13:31250444
|
G | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+2478G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250444 | ||||||
| chr13:31250470
|
T | C | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.459+2504T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250470 | ||||||
| chr13:31250513
|
C | T | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+2547C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250513 | ||||||
| chr13:31250581
|
A | G | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.459+2615A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250581 | ||||||
| chr13:31250669
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.459+2703C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250669 | ||||||
| chr13:31250685
|
G | A | 154 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.459+2719G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250685 | ||||||
| chr13:31250711
|
G | A | 25 | a0001c0001t0001g0192a0001c0001t0004g0173a0001c0001t0005g0001others(22): Show | 26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+2745G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250711 | ||||||
| chr13:31250847
|
A | G | 24 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(21): Show | 25 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+2881A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250847 | ||||||
| chr13:31250950
|
C | G | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+2984C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250950 | ||||||
| chr13:31251020
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.459+3054A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251020 | ||||||
| chr13:31251033
|
T | G | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 73 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.459+3067T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251033 | ||||||
| chr13:31251049
|
C | G | 2 | a0002c0002t0002g0144a0002c0002t0002g0234 | 2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.459+3083C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251049 | ||||||
| chr13:31251085
|
G | T | 2 | a0001c0013t0001g0262a0002c0003t0021g0068 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.459+3119G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251085 | ||||||
| chr13:31251146
|
TAAAC | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3182_459+3185d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31251146 | |||||
| chr13:31251214
|
C | G | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459+3248C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251214 | ||||||
| chr13:31251264
|
T | C | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+3298T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251264 | ||||||
| chr13:31251446
|
G | A | 226 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.459+3480G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251446 | ||||||
| chr13:31251447
|
T | C | 1 | a0002c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.459+3481T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251447 | ||||||
| chr13:31251670
|
GAA | G | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.459+3705_459+3706d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251670 | ||||||
| chr13:31251807
|
C | T | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.459+3841C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251807 | ||||||
| chr13:31251964
|
GA | G | 25 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(22): Show | 26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+3999delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251964 | ||||||
| chr13:31252257
|
C | G | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+4291C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252257 | ||||||
| chr13:31252286
|
G | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+4320G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252286 | ||||||
| chr13:31252287
|
A | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+4321A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252287 | ||||||
| chr13:31252362
|
A | G | 1 | a0002c0002t0002g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.459+4396A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252362 | ||||||
| chr13:31252400
|
T | C | 155 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.459+4434T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252400 | ||||||
| chr13:31252404
|
G | A | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+4438G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252404 | ||||||
| chr13:31252423
|
C | A | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.459+4457C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252423 | ||||||
| chr13:31252494
|
C | G | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.459+4528C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252494 | ||||||
| chr13:31252543
|
CA | C | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+4586delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31252543 | |||||
| chr13:31252555
|
G | A | 1 | a0002c0002t0008g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.459+4589G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252555 | ||||||
| chr13:31252594
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459+4628A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252594 | ||||||
| chr13:31252698
|
G | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4732G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252698 | ||||||
| chr13:31252701
|
C | A | 1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4735C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252701 | ||||||
| chr13:31252702
|
C | G | 1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4736C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252702 | ||||||
| chr13:31252703
|
C | A | 1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4737C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252703 | ||||||
| chr13:31252704
|
A | C | 1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4738A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252704 | ||||||
| chr13:31252705
|
G | C | 1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4739G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252705 | ||||||
| chr13:31252797
|
G | C | 7 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0263others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+4831G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252797 | ||||||
| chr13:31253070
|
G | A | 1 | a0002c0002t0006g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.459+5104G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253070 | ||||||
| chr13:31253130
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459+5164C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253130 | ||||||
| chr13:31253131
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+5165G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253131 | ||||||
| chr13:31253373
|
C | T | 25 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(22): Show | 26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+5407C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253373 | ||||||
| chr13:31253434
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.459+5468G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253434 | ||||||
| chr13:31253466
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459+5500G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253466 | ||||||
| chr13:31253467
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459+5501C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253467 | ||||||
| chr13:31253485
|
C | T | 1 | a0002c0002t0003g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.459+5519C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253485 | ||||||
| chr13:31253512
|
G | T | 4 | a0001c0001t0001g0178a0002c0002t0004g0172a0002c0002t0004g0182others(1): Show | 4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+5546G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253512 | ||||||
| chr13:31253542
|
T | G | 226 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.459+5576T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253542 | ||||||
| chr13:31253544
|
T | C | 255 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.459+5578T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253544 | ||||||
| chr13:31253595
|
C | CA | 34 | a0001c0001t0001g0022a0001c0001t0001g0192a0001c0001t0001g0193others(31): Show | 35 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.459+5655dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAA | 17 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0005g0198others(14): Show | 17 | HG00741.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+5654_459+5655d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(8): Show |
1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.459+5641_459+5655d others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(9): Show |
1 | a0002c0002t0012g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.459+5640_459+5655d others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0178 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.459+5639_459+5655d others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(11): Show |
1 | a0002c0002t0004g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.459+5638_459+5655d others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(14): Show |
1 | a0002c0002t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+5635_459+5655d others(23): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
C | CAAAAAAA others(16): Show |
2 | a0002c0002t0012g0176a0002c0011t0004g0181 | 2 | HG01106.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.459+5633_459+5655d others(25): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
CAA | C | 55 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(52): Show | 56 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.459+5654_459+5655d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253595
|
CAAA | C | 6 | a0002c0002t0002g0266a0002c0002t0003g0078a0002c0002t0003g0241others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+5653_459+5655d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | |||||
| chr13:31253613
|
A | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+5647A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253613 | ||||||
| chr13:31253618
|
A | AAAAAACA others(3): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0237 | 2 | HG02300.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+5655_459+5656i others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | |||||
| chr13:31253618
|
A | AAAAACAA others(2): Show |
28 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0089others(25): Show | 28 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+5655_459+5656i others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | |||||
| chr13:31253618
|
A | AAAACAAA others(1): Show |
88 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0062others(85): Show | 88 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.459+5656_459+5657i others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | |||||
| chr13:31253618
|
A | C | 5 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+5652A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253618 | ||||||
| chr13:31253640
|
G | A | 255 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.459+5674G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253640 | ||||||
| chr13:31253911
|
A | G | 1 | a0001c0001t0015g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.459+5945A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253911 | ||||||
| chr13:31253986
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6020G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253986 | ||||||
| chr13:31254059
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6093C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254059 | ||||||
| chr13:31254142
|
A | G | 6 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0263others(3): Show | 6 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+6176A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254142 | ||||||
| chr13:31254230
|
G | A | 226 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.459+6264G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254230 | ||||||
| chr13:31254292
|
T | C | 257 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.459+6326T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254292 | ||||||
| chr13:31254327
|
A | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6361A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254327 | ||||||
| chr13:31254364
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6398G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254364 | ||||||
| chr13:31254372
|
T | C | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+6406T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254372 | ||||||
| chr13:31254617
|
T | C | 1 | a0003c0004t0004g0205 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.460-6329T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254617 | ||||||
| chr13:31254837
|
G | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-6109G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254837 | ||||||
| chr13:31254847
|
T | G | 1 | a0002c0002t0003g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.460-6099T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254847 | ||||||
| chr13:31254910
|
G | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-6036G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254910 | ||||||
| chr13:31254968
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0106 | 3 | NA18950.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.460-5978C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254968 | ||||||
| chr13:31254989
|
A | G | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-5957A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254989 | ||||||
| chr13:31255023
|
CA | C | 155 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.460-5920delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255023 | |||||
| chr13:31255029
|
C | T | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.460-5917C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255029 | ||||||
| chr13:31255037
|
C | CA | 26 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(23): Show | 26 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-5892dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255037 | |||||
| chr13:31255037
|
CA | C | 152 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.460-5892delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255037 | |||||
| chr13:31255051
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.460-5895A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255051 | ||||||
| chr13:31255054
|
A | G | 1 | a0002c0002t0003g0002 | 2 | HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.460-5892A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255054 | ||||||
| chr13:31255450
|
A | G | 2 | a0001c0001t0014g0186a0002c0002t0003g0088 | 2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.460-5496A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255450 | ||||||
| chr13:31255505
|
G | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-5441G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255505 | ||||||
| chr13:31255579
|
G | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-5367G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255579 | ||||||
| chr13:31255620
|
A | G | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460-5326A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255620 | ||||||
| chr13:31255669
|
C | G | 2 | a0002c0002t0002g0195a0002c0002t0002g0196 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.460-5277C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255669 | ||||||
| chr13:31255841
|
T | C | 226 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.460-5105T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255841 | ||||||
| chr13:31255874
|
A | G | 198 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.460-5072A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255874 | ||||||
| chr13:31255899
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-5047C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255899 | ||||||
| chr13:31256096
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0102others(1): Show | 4 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-4850G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256096 | ||||||
| chr13:31256173
|
T | C | 1 | a0001c0013t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.460-4773T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256173 | ||||||
| chr13:31256227
|
A | G | 2 | a0002c0002t0003g0229a0002c0002t0003g0240 | 2 | HG01496.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.460-4719A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256227 | ||||||
| chr13:31256278
|
A | G | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-4668A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256278 | ||||||
| chr13:31256497
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-4449C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256497 | ||||||
| chr13:31256544
|
T | C | 1 | a0002c0002t0003g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-4402T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256544 | ||||||
| chr13:31256728
|
C | T | 3 | a0001c0001t0004g0173a0001c0001t0004g0218a0002c0002t0002g0235 | 3 | HG01891.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.460-4218C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256728 | ||||||
| chr13:31256755
|
C | G | 3 | a0001c0001t0001g0175a0002c0002t0012g0174a0002c0002t0012g0176 | 3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.460-4191C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256755 | ||||||
| chr13:31256911
|
TA | T | 115 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.460-4023delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31256911 | |||||
| chr13:31256955
|
A | G | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-3991A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256955 | ||||||
| chr13:31257112
|
A | G | 1 | a0002c0002t0002g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.460-3834A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257112 | ||||||
| chr13:31257302
|
A | C | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-3644A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257302 | ||||||
| chr13:31257380
|
G | A | 57 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-3566G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257380 | ||||||
| chr13:31257410
|
A | G | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.460-3536A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257410 | ||||||
| chr13:31257503
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3443C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257503 | ||||||
| chr13:31257917
|
A | G | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-3029A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257917 | ||||||
| chr13:31257940
|
A | G | 255 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.460-3006A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257940 | ||||||
| chr13:31257994
|
T | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2952T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257994 | ||||||
| chr13:31258000
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2946G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258000 | ||||||
| chr13:31258016
|
C | G | 1 | a0001c0001t0007g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.460-2930C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258016 | ||||||
| chr13:31258056
|
A | G | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2890A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258056 | ||||||
| chr13:31258282
|
C | G | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.460-2664C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258282 | ||||||
| chr13:31258292
|
T | C | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(32): Show | 35 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.460-2654T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258292 | ||||||
| chr13:31258388
|
G | A | 27 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(24): Show | 28 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.460-2558G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258388 | ||||||
| chr13:31258445
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2501C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258445 | ||||||
| chr13:31258446
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.460-2500G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258446 | ||||||
| chr13:31258594
|
A | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2352A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258594 | ||||||
| chr13:31259133
|
G | A | 3 | a0001c0001t0001g0175a0002c0002t0012g0174a0002c0002t0012g0176 | 3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.460-1813G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259133 | ||||||
| chr13:31259136
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-1810C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259136 | ||||||
| chr13:31259284
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-1662G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259284 | ||||||
| chr13:31259335
|
G | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-1611G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259335 | ||||||
| chr13:31259352
|
TTCC | T | 5 | a0002c0002t0003g0009a0002c0002t0003g0031a0002c0002t0003g0033others(2): Show | 5 | HG01243.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1592_460-1590d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31259352 | |||||
| chr13:31259396
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.460-1550G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259396 | ||||||
| chr13:31259441
|
C | G | 58 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(55): Show | 59 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.460-1505C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259441 | ||||||
| chr13:31259498
|
G | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.460-1448G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259498 | ||||||
| chr13:31259540
|
CT | C | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.460-1399delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31259540 | |||||
| chr13:31259587
|
A | G | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1359A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259587 | ||||||
| chr13:31259835
|
T | A | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1111T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259835 | ||||||
| chr13:31259850
|
T | C | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460-1096T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259850 | ||||||
| chr13:31260150
|
A | C | 1 | a0002c0002t0009g0013 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.460-796A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260150 | ||||||
| chr13:31260291
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.460-655T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260291 | ||||||
| chr13:31260358
|
T | C | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-588T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260358 | ||||||
| chr13:31260445
|
G | T | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-501G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260445 | ||||||
| chr13:31260634
|
G | T | 1 | a0002c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-312G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260634 | ||||||
| chr13:31260874
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0237 | 3 | HG03834.hp1 HG03927.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.460-72T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260874 | ||||||
| chr13:31261125
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.596+43G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261125 | ||||||
| chr13:31261127
|
A | G | 1 | a0002c0002t0002g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.596+45A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261127 | ||||||
| chr13:31261131
|
AC | A | 57 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+50delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261131 | ||||||
| chr13:31261163
|
A | C | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.596+81A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261163 | ||||||
| chr13:31261214
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.596+132C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261214 | ||||||
| chr13:31261238
|
G | A | 126 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.596+156G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261238 | ||||||
| chr13:31261254
|
G | A | 1 | a0001c0001t0004g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.596+172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261254 | ||||||
| chr13:31261449
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.596+367A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261449 | ||||||
| chr13:31261471
|
A | G | 27 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(24): Show | 28 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.596+389A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261471 | ||||||
| chr13:31261647
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.596+565A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261647 | ||||||
| chr13:31262096
|
C | T | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.596+1014C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262096 | ||||||
| chr13:31262130
|
G | A | 1 | a0002c0002t0002g0017 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.596+1048G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262130 | ||||||
| chr13:31262165
|
G | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(53): Show | 57 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.596+1083G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262165 | ||||||
| chr13:31262230
|
G | T | 124 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.596+1148G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262230 | ||||||
| chr13:31262341
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1259C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262341 | ||||||
| chr13:31262424
|
C | T | 1 | a0001c0001t0005g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.596+1342C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262424 | ||||||
| chr13:31262526
|
C | T | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1444C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262526 | ||||||
| chr13:31262599
|
CTT | C | 29 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.596+1519_596+1520d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31262599 | |||||
| chr13:31262631
|
T | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.596+1549T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262631 | ||||||
| chr13:31262633
|
C | G | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(70): Show | 74 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.596+1551C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262633 | ||||||
| chr13:31262644
|
A | T | 57 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+1562A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262644 | ||||||
| chr13:31263064
|
C | T | 3 | a0001c0001t0004g0173a0001c0001t0004g0218a0002c0002t0002g0235 | 3 | HG01891.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.596+1982C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263064 | ||||||
| chr13:31263101
|
G | A | 5 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0003g0259others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+2019G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263101 | ||||||
| chr13:31263229
|
C | T | 3 | a0002c0002t0002g0087a0002c0002t0002g0095a0002c0002t0002g0216 | 3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.596+2147C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263229 | ||||||
| chr13:31263283
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.596+2201C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263283 | ||||||
| chr13:31263411
|
A | G | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+2329A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263411 | ||||||
| chr13:31263419
|
G | A | 57 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+2337G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263419 | ||||||
| chr13:31263436
|
T | C | 3 | a0002c0002t0002g0127a0002c0002t0002g0137a0002c0002t0002g0140 | 3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.596+2354T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263436 | ||||||
| chr13:31263832
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+2750G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263832 | ||||||
| chr13:31264030
|
G | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.596+2948G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264030 | ||||||
| chr13:31264162
|
C | T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.596+3080C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264162 | ||||||
| chr13:31264319
|
C | T | 1 | a0001c0013t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.596+3237C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264319 | ||||||
| chr13:31264350
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.596+3268C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264350 | ||||||
| chr13:31264365
|
C | T | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+3283C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264365 | ||||||
| chr13:31264379
|
T | C | 153 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.596+3297T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264379 | ||||||
| chr13:31264423
|
G | A | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+3341G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264423 | ||||||
| chr13:31264505
|
A | G | 6 | a0002c0002t0001g0252a0002c0002t0003g0094a0002c0002t0003g0246others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+3423A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264505 | ||||||
| chr13:31264551
|
A | G | 214 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.596+3469A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264551 | ||||||
| chr13:31264590
|
A | G | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.596+3508A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264590 | ||||||
| chr13:31264691
|
T | C | 1 | a0004c0005t0001g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.596+3609T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264691 | ||||||
| chr13:31264731
|
C | G | 214 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.596+3649C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264731 | ||||||
| chr13:31264755
|
C | T | 9 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0004g0172others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+3673C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264755 | ||||||
| chr13:31264827
|
A | T | 1 | a0002c0010t0003g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.596+3745A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264827 | ||||||
| chr13:31264836
|
C | A | 4 | a0001c0001t0001g0178a0002c0002t0004g0172a0002c0002t0004g0182others(1): Show | 4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+3754C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264836 | ||||||
| chr13:31264928
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.596+3846C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264928 | ||||||
| chr13:31265137
|
G | A | 122 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.596+4055G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265137 | ||||||
| chr13:31265151
|
A | C | 9 | a0001c0001t0001g0175a0001c0001t0001g0178a0002c0002t0004g0172others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-4063A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265151 | ||||||
| chr13:31265165
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0168a0001c0001t0025g0261 | 3 | HG02056.hp2 HG02896.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.597-4049C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265165 | ||||||
| chr13:31265293
|
C | A | 21 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0004g0173others(18): Show | 22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.597-3921C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265293 | ||||||
| chr13:31265556
|
C | T | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.597-3658C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265556 | ||||||
| chr13:31265832
|
TGGAAGTG others(19): Show |
T | 1 | a0001c0001t0004g0053 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.597-3361_597-3336d others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31265832 | |||||
| chr13:31266053
|
A | G | 192 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.597-3161A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266053 | ||||||
| chr13:31266091
|
G | A | 2 | a0002c0002t0003g0240a0002c0003t0021g0068 | 2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.597-3123G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266091 | ||||||
| chr13:31266123
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0046 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.597-3091G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266123 | ||||||
| chr13:31266127
|
A | C | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597-3087A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266127 | ||||||
| chr13:31266155
|
A | G | 1 | a0002c0002t0002g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.597-3059A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266155 | ||||||
| chr13:31266172
|
G | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.597-3042G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266172 | ||||||
| chr13:31266182
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.597-3032T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266182 | ||||||
| chr13:31266199
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.597-3015C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266199 | ||||||
| chr13:31266216
|
C | T | 2 | a0001c0001t0007g0016a0001c0001t0007g0149 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.597-2998C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266216 | ||||||
| chr13:31266219
|
C | A | 1 | a0001c0001t0007g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.597-2995C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266219 | ||||||
| chr13:31266249
|
T | C | 4 | a0002c0003t0003g0026a0002c0003t0003g0228a0005c0006t0003g0226others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-2965T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266249 | ||||||
| chr13:31266264
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-2950G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266264 | ||||||
| chr13:31266270
|
C | T | 1 | a0001c0001t0010g0110 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.597-2944C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266270 | ||||||
| chr13:31266324
|
G | A | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.597-2890G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266324 | ||||||
| chr13:31266325
|
G | A | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.597-2889G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266325 | ||||||
| chr13:31266436
|
A | G | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.597-2778A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266436 | ||||||
| chr13:31266568
|
A | T | 2 | a0001c0001t0004g0218a0002c0002t0002g0235 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.597-2646A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266568 | ||||||
| chr13:31266569
|
C | G | 1 | a0001c0013t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.597-2645C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266569 | ||||||
| chr13:31266719
|
A | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.597-2495A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266719 | ||||||
| chr13:31266792
|
A | G | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.597-2422A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266792 | ||||||
| chr13:31267190
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597-2024C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267190 | ||||||
| chr13:31267217
|
T | C | 2 | a0002c0002t0003g0229a0002c0002t0018g0253 | 2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.597-1997T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267217 | ||||||
| chr13:31267252
|
G | C | 1 | a0006c0012t0004g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.597-1962G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267252 | ||||||
| chr13:31267315
|
G | A | 22 | a0001c0013t0001g0262a0002c0002t0002g0029a0002c0002t0002g0030others(19): Show | 22 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.597-1899G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267315 | ||||||
| chr13:31267340
|
C | A | 3 | a0002c0002t0002g0127a0002c0002t0002g0137a0002c0002t0002g0140 | 3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.597-1874C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267340 | ||||||
| chr13:31267757
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.597-1457C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267757 | ||||||
| chr13:31267768
|
C | T | 15 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(12): Show | 15 | HG00639.hp1 HG01243.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-1446C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267768 | ||||||
| chr13:31267851
|
C | CT | 5 | a0002c0002t0002g0266a0002c0002t0003g0250a0002c0002t0011g0005others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-1350dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31267851 | |||||
| chr13:31268009
|
A | T | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(69): Show | 74 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.597-1205A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268009 | ||||||
| chr13:31268046
|
A | G | 1 | a0002c0002t0002g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.597-1168A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268046 | ||||||
| chr13:31268354
|
T | C | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.597-860T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268354 | ||||||
| chr13:31268533
|
T | C | 1 | a0001c0001t0007g0028 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.597-681T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268533 | ||||||
| chr13:31268633
|
C | T | 4 | a0002c0003t0003g0026a0002c0003t0003g0228a0005c0006t0003g0226others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-581C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268633 | ||||||
| chr13:31268683
|
T | C | 1 | a0002c0002t0002g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597-531T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268683 | ||||||
| chr13:31268966
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.597-248T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268966 | ||||||
| chr13:31269050
|
C | T | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.597-164C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31269050 | ||||||
| chr13:31269183
|
TA | T | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 69 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.597-23delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31269183 | |||||
| chr13:31269360
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+83A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269360 | ||||||
| chr13:31269461
|
A | G | 153 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.660+184A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269461 | ||||||
| chr13:31269489
|
A | G | 21 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.660+212A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269489 | ||||||
| chr13:31269527
|
A | G | 252 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(249): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.660+250A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269527 | ||||||
| chr13:31269601
|
C | T | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.660+324C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269601 | ||||||
| chr13:31269602
|
G | A | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 69 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.660+325G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269602 | ||||||
| chr13:31269642
|
CG | C | 90 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(87): Show | 91 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.660+366delG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269642 | ||||||
| chr13:31269643
|
G | C | 159 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.660+366G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269643 | ||||||
| chr13:31269643
|
G | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+366G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269643 | ||||||
| chr13:31269645
|
C | A | 152 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.660+368C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269645 | ||||||
| chr13:31269650
|
T | A | 13 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(10): Show | 13 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.660+373T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269650 | ||||||
| chr13:31269650
|
T | C | 19 | a0002c0002t0003g0259a0002c0002t0004g0172a0002c0002t0004g0177others(16): Show | 19 | HG01106.hp2 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.660+373T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269650 | ||||||
| chr13:31269755
|
C | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.660+478C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269755 | ||||||
| chr13:31269772
|
G | T | 2 | a0002c0002t0003g0229a0002c0002t0018g0253 | 2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.660+495G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269772 | ||||||
| chr13:31269810
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.660+533C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269810 | ||||||
| chr13:31269934
|
C | G | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.660+657C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269934 | ||||||
| chr13:31269951
|
C | T | 251 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.660+674C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269951 | ||||||
| chr13:31269983
|
C | T | 68 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(65): Show | 69 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.660+706C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269983 | ||||||
| chr13:31270283
|
A | T | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.660+1006A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270283 | ||||||
| chr13:31270346
|
T | C | 1 | a0002c0002t0004g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.660+1069T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270346 | ||||||
| chr13:31270444
|
A | G | 2 | a0002c0002t0012g0174a0002c0002t0012g0176 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.660+1167A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270444 | ||||||
| chr13:31270618
|
G | T | 229 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.660+1341G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270618 | ||||||
| chr13:31270663
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.660+1386G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270663 | ||||||
| chr13:31270934
|
AAG | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+1662_660+1663d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31270934 | |||||
| chr13:31271237
|
T | C | 4 | a0002c0003t0003g0026a0002c0003t0003g0228a0005c0006t0003g0226others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1960T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271237 | ||||||
| chr13:31271265
|
A | T | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+1988A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271265 | ||||||
| chr13:31271331
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.660+2054C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271331 | ||||||
| chr13:31271669
|
C | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.660+2392C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271669 | ||||||
| chr13:31271751
|
T | G | 1 | a0002c0002t0002g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.660+2474T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271751 | ||||||
| chr13:31271879
|
A | G | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+2602A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271879 | ||||||
| chr13:31271983
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.661-2526T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271983 | ||||||
| chr13:31271992
|
T | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-2517T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271992 | ||||||
| chr13:31272218
|
C | CT | 161 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.661-2276dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31272218 | |||||
| chr13:31272316
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661-2193A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272316 | ||||||
| chr13:31272363
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.661-2146C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272363 | ||||||
| chr13:31272744
|
CTTG | C | 2 | a0001c0001t0004g0038a0001c0001t0004g0061 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.661-1759_661-1757d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31272744 | |||||
| chr13:31272836
|
T | A | 1 | a0002c0002t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.661-1673T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272836 | ||||||
| chr13:31272903
|
T | C | 6 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(3): Show | 6 | HG01106.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-1606T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272903 | ||||||
| chr13:31273027
|
A | G | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.661-1482A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273027 | ||||||
| chr13:31273089
|
T | C | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.661-1420T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273089 | ||||||
| chr13:31273094
|
CTTTGTTT others(7): Show |
C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-1414_661-1401d others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273094 | ||||||
| chr13:31273176
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1333C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273176 | ||||||
| chr13:31273187
|
C | T | 75 | a0001c0001t0001g0069a0001c0001t0001g0117a0001c0001t0001g0118others(72): Show | 76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.661-1322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273187 | ||||||
| chr13:31273205
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.661-1304C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273205 | ||||||
| chr13:31273240
|
G | A | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.661-1269G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273240 | ||||||
| chr13:31273273
|
T | C | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.661-1236T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273273 | ||||||
| chr13:31273374
|
G | A | 1 | a0001c0001t0005g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.661-1135G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273374 | ||||||
| chr13:31273431
|
A | T | 1 | a0002c0002t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.661-1078A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273431 | ||||||
| chr13:31273502
|
AATTTT | A | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(73): Show | 77 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.661-1004_661-1000d others(7): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31273502 | |||||
| chr13:31273610
|
A | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-899A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273610 | ||||||
| chr13:31273612
|
T | A | 2 | a0002c0002t0003g0025a0002c0002t0017g0019 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.661-897T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273612 | ||||||
| chr13:31273751
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0124 | 2 | NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.661-758T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273751 | ||||||
| chr13:31273774
|
T | A | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.661-735T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273774 | ||||||
| chr13:31273831
|
T | A | 1 | a0001c0001t0007g0028 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.661-678T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273831 | ||||||
| chr13:31273959
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.661-550A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273959 | ||||||
| chr13:31274246
|
A | G | 20 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0067others(17): Show | 21 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.661-263A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274246 | ||||||
| chr13:31274318
|
G | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-191G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274318 | ||||||
| chr13:31274398
|
G | A | 248 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.661-111G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274398 | ||||||
| chr13:31274686
|
A | G | 73 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(70): Show | 74 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.780+58A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31274686 | ||||||
| chr13:31275216
|
A | G | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.780+588A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275216 | ||||||
| chr13:31275250
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+622T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275250 | ||||||
| chr13:31275268
|
A | G | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.780+640A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275268 | ||||||
| chr13:31275313
|
C | T | 1 | a0002c0002t0003g0241 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.780+685C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275313 | ||||||
| chr13:31275394
|
C | T | 142 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(139): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.780+766C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275394 | ||||||
| chr13:31275403
|
G | T | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.780+775G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275403 | ||||||
| chr13:31275434
|
A | C | 142 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(139): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.780+806A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275434 | ||||||
| chr13:31275675
|
A | G | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.781-1027A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275675 | ||||||
| chr13:31275713
|
C | T | 140 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.781-989C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275713 | ||||||
| chr13:31275852
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781-850G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275852 | ||||||
| chr13:31276148
|
C | G | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.781-554C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276148 | ||||||
| chr13:31276197
|
G | T | 20 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(17): Show | 20 | HG00639.hp1 HG01243.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.781-505G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276197 | ||||||
| chr13:31276203
|
C | T | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.781-499C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276203 | ||||||
| chr13:31276225
|
G | A | 1 | a0002c0002t0004g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.781-477G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276225 | ||||||
| chr13:31276577
|
G | C | 248 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.781-125G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276577 | ||||||
| chr13:31276580
|
G | A | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.781-122G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276580 | ||||||
| chr13:31276666
|
C | CACAT | 14 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0067others(11): Show | 15 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.781-34_781-31dupCA others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr13 | 31276666 | |||||
| chr13:31276852
|
G | A | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.850+81G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31276852 | ||||||
| chr13:31276922
|
A | G | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.850+151A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31276922 | ||||||
| chr13:31277062
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.850+291G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277062 | ||||||
| chr13:31277171
|
G | T | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+400G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277171 | ||||||
| chr13:31277190
|
A | G | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850+419A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277190 | ||||||
| chr13:31277218
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.850+447T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277218 | ||||||
| chr13:31277389
|
TA | T | 19 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(16): Show | 19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+629delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31277389 | |||||
| chr13:31277751
|
C | A | 4 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0158others(1): Show | 4 | HG00558.hp1 NA18983.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+980C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277751 | ||||||
| chr13:31277824
|
G | T | 1 | a0002c0002t0020g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+1053G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277824 | ||||||
| chr13:31277997
|
T | G | 1 | a0002c0002t0003g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.850+1226T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277997 | ||||||
| chr13:31278056
|
C | T | 7 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(4): Show | 7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1285C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278056 | ||||||
| chr13:31278088
|
G | A | 70 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.850+1317G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278088 | ||||||
| chr13:31278139
|
A | G | 140 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.850+1368A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278139 | ||||||
| chr13:31278248
|
T | C | 76 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(73): Show | 77 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.850+1477T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278248 | ||||||
| chr13:31278422
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.850+1651A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278422 | ||||||
| chr13:31278426
|
C | T | 1 | a0002c0002t0003g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.850+1655C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278426 | ||||||
| chr13:31278760
|
A | T | 151 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(148): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.850+1989A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278760 | ||||||
| chr13:31279117
|
T | C | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.850+2346T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279117 | ||||||
| chr13:31279146
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0102others(2): Show | 5 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2375C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279146 | ||||||
| chr13:31279244
|
A | G | 1 | a0002c0002t0003g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850+2473A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279244 | ||||||
| chr13:31279264
|
C | G | 1 | a0002c0002t0003g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850+2493C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279264 | ||||||
| chr13:31279493
|
G | A | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+2722G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279493 | ||||||
| chr13:31279504
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.850+2733A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279504 | ||||||
| chr13:31279543
|
C | T | 1 | a0001c0001t0006g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.850+2772C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279543 | ||||||
| chr13:31279582
|
G | A | 4 | a0002c0002t0002g0266a0002c0002t0011g0005a0002c0002t0011g0006others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+2811G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279582 | ||||||
| chr13:31279620
|
G | A | 7 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(4): Show | 7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+2849G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279620 | ||||||
| chr13:31279697
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.850+2926G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279697 | ||||||
| chr13:31279811
|
C | G | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.850+3040C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279811 | ||||||
| chr13:31279811
|
C | T | 2 | a0002c0002t0002g0082a0002c0002t0002g0111 | 2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850+3040C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279811 | ||||||
| chr13:31279845
|
C | T | 1 | a0002c0002t0002g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.850+3074C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279845 | ||||||
| chr13:31279858
|
C | T | 1 | a0002c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850+3087C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279858 | ||||||
| chr13:31279985
|
A | G | 2 | a0001c0001t0014g0186a0002c0002t0002g0235 | 2 | HG01255.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.850+3214A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279985 | ||||||
| chr13:31280051
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.850+3280C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280051 | ||||||
| chr13:31280183
|
A | G | 1 | a0002c0002t0011g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850+3412A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280183 | ||||||
| chr13:31280357
|
T | G | 19 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(16): Show | 19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+3586T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280357 | ||||||
| chr13:31280360
|
G | A | 1 | a0002c0003t0002g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.850+3589G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280360 | ||||||
| chr13:31280380
|
C | T | 1 | a0002c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850+3609C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280380 | ||||||
| chr13:31280480
|
G | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.850+3709G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280480 | ||||||
| chr13:31280556
|
G | A | 70 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(67): Show | 71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.850+3785G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280556 | ||||||
| chr13:31280607
|
G | A | 19 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(16): Show | 19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+3836G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280607 | ||||||
| chr13:31280922
|
C | T | 1 | a0001c0001t0006g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.851-3726C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280922 | ||||||
| chr13:31281119
|
G | A | 2 | a0002c0002t0003g0243a0002c0002t0003g0244 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.851-3529G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281119 | ||||||
| chr13:31281126
|
C | A | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.851-3522C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281126 | ||||||
| chr13:31281209
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.851-3439G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281209 | ||||||
| chr13:31281755
|
C | A | 1 | a0002c0002t0020g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851-2893C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281755 | ||||||
| chr13:31282019
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.851-2629C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282019 | ||||||
| chr13:31282378
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-2270G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282378 | ||||||
| chr13:31282406
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.851-2242G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282406 | ||||||
| chr13:31282411
|
G | A | 70 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(67): Show | 71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.851-2237G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282411 | ||||||
| chr13:31282415
|
G | A | 1 | a0001c0001t0006g0056 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.851-2233G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282415 | ||||||
| chr13:31282456
|
G | A | 2 | a0001c0001t0004g0044a0001c0001t0004g0053 | 2 | NA18963.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.851-2192G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282456 | ||||||
| chr13:31282503
|
G | A | 1 | a0001c0001t0007g0028 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.851-2145G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282503 | ||||||
| chr13:31282511
|
G | A | 7 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(4): Show | 7 | HG02015.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-2137G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282511 | ||||||
| chr13:31282515
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.851-2133G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282515 | ||||||
| chr13:31282617
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-2031G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282617 | ||||||
| chr13:31282629
|
G | A | 1 | a0002c0002t0008g0096 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.851-2019G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282629 | ||||||
| chr13:31282649
|
C | CA | 148 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(145): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.851-1982dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | |||||
| chr13:31282649
|
C | CAA | 6 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0168others(3): Show | 6 | HG02055.hp2 HG02056.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-1983_851-1982d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | |||||
| chr13:31282649
|
C | CAAA | 7 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0221others(4): Show | 7 | HG00639.hp1 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-1984_851-1982d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | |||||
| chr13:31282649
|
CA | C | 75 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(72): Show | 76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-1982delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | |||||
| chr13:31282941
|
G | A | 7 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(4): Show | 7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-1707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282941 | ||||||
| chr13:31283138
|
G | C | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.851-1510G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283138 | ||||||
| chr13:31283282
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-1366C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283282 | ||||||
| chr13:31283288
|
G | A | 76 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(73): Show | 77 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.851-1360G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283288 | ||||||
| chr13:31283293
|
G | A | 1 | a0001c0001t0014g0036 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.851-1355G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283293 | ||||||
| chr13:31283597
|
G | GT | 166 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.851-1044dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31283597 | |||||
| chr13:31283604
|
T | TTA | 74 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(71): Show | 75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.851-1044_851-1043i others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283604 | ||||||
| chr13:31283657
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.851-991A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283657 | ||||||
| chr13:31283723
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-925T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283723 | ||||||
| chr13:31283747
|
T | A | 1 | a0002c0002t0003g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.851-901T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283747 | ||||||
| chr13:31283786
|
T | C | 1 | a0004c0005t0001g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.851-862T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283786 | ||||||
| chr13:31283837
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851-811C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283837 | ||||||
| chr13:31284099
|
A | G | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.851-549A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284099 | ||||||
| chr13:31284205
|
G | A | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.851-443G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284205 | ||||||
| chr13:31284290
|
C | T | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-358C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284290 | ||||||
| chr13:31284320
|
G | C | 17 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0080others(14): Show | 17 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.851-328G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284320 | ||||||
| chr13:31284348
|
C | T | 1 | a0002c0002t0003g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.851-300C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284348 | ||||||
| chr13:31284902
|
T | A | 76 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(73): Show | 77 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.964+141T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31284902 | ||||||
| chr13:31285241
|
G | C | 3 | a0001c0001t0007g0016a0002c0002t0003g0025a0002c0002t0017g0019 | 3 | HG00738.hp1 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.964+480G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285241 | ||||||
| chr13:31285358
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+597G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285358 | ||||||
| chr13:31285604
|
T | TA | 11 | a0002c0002t0002g0087a0002c0002t0002g0095a0002c0002t0002g0111others(8): Show | 11 | HG01106.hp2 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+869dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | |||||
| chr13:31285604
|
TA | T | 139 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.964+869delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | |||||
| chr13:31285604
|
TAAA | T | 6 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(3): Show | 6 | HG02015.hp1 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+867_964+869del others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | |||||
| chr13:31285604
|
TAAAAA | T | 62 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(59): Show | 63 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.964+865_964+869del others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | |||||
| chr13:31285604
|
TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.964+860_964+869del others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | |||||
| chr13:31285625
|
A | G | 1 | a0002c0002t0002g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.964+864A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285625 | ||||||
| chr13:31285695
|
C | A | 239 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.964+934C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285695 | ||||||
| chr13:31285695
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.964+934C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285695 | ||||||
| chr13:31285799
|
A | G | 1 | a0002c0002t0003g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.965-921A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285799 | ||||||
| chr13:31285810
|
C | T | 1 | a0002c0002t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.965-910C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285810 | ||||||
| chr13:31285847
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.965-873A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285847 | ||||||
| chr13:31285850
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.965-870C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285850 | ||||||
| chr13:31286121
|
A | G | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.965-599A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286121 | ||||||
| chr13:31286144
|
A | G | 1 | a0002c0002t0002g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.965-576A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286144 | ||||||
| chr13:31286262
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-458C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286262 | ||||||
| chr13:31286287
|
C | T | 1 | a0001c0001t0006g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.965-433C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286287 | ||||||
| chr13:31286330
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.965-390G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286330 | ||||||
| chr13:31286541
|
TCC | T | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-177_965-176del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31286541 | |||||
| chr13:31286546
|
C | T | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-174C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286546 | ||||||
| chr13:31286548
|
G | A | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286548 | ||||||
| chr13:31286549
|
G | T | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-171G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286549 | ||||||
| chr13:31286550
|
T | C | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-170T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286550 | ||||||
| chr13:31286632
|
G | C | 76 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(73): Show | 77 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.965-88G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286632 | ||||||
| chr13:31286829
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+10C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286829 | ||||||
| chr13:31286922
|
G | A | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1064+103G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286922 | ||||||
| chr13:31286993
|
T | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+174T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286993 | ||||||
| chr13:31287141
|
C | T | 2 | a0001c0001t0005g0201a0002c0002t0003g0241 | 2 | HG02165.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1064+322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287141 | ||||||
| chr13:31287142
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1064+323G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287142 | ||||||
| chr13:31287270
|
A | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+451A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287270 | ||||||
| chr13:31287338
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1064+519G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287338 | ||||||
| chr13:31287349
|
G | A | 1 | a0001c0001t0006g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1064+530G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287349 | ||||||
| chr13:31287386
|
G | A | 3 | a0002c0002t0002g0087a0002c0002t0002g0095a0002c0002t0002g0216 | 3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+567G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287386 | ||||||
| chr13:31287467
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+648C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287467 | ||||||
| chr13:31287634
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+815G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287634 | ||||||
| chr13:31287663
|
A | G | 2 | a0002c0002t0003g0243a0002c0002t0003g0244 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1064+844A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287663 | ||||||
| chr13:31287669
|
G | GA | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1064+858dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31287669 | |||||
| chr13:31287677
|
AT | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121others(2): Show | 5 | HG02027.hp2 HG02129.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+860delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31287677 | |||||
| chr13:31287727
|
T | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+908T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287727 | ||||||
| chr13:31287730
|
T | C | 1 | a0002c0002t0002g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1064+911T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287730 | ||||||
| chr13:31287773
|
T | C | 1 | a0002c0002t0008g0083 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1064+954T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287773 | ||||||
| chr13:31287833
|
A | G | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1064+1014A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287833 | ||||||
| chr13:31287932
|
A | G | 11 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1064+1113A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287932 | ||||||
| chr13:31287935
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1064+1116A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287935 | ||||||
| chr13:31288015
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1064+1196G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288015 | ||||||
| chr13:31288038
|
G | C | 17 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0080others(14): Show | 17 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1064+1219G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288038 | ||||||
| chr13:31288197
|
C | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+1378C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288197 | ||||||
| chr13:31288335
|
A | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+1516A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288335 | ||||||
| chr13:31288369
|
A | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+1550A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288369 | ||||||
| chr13:31288380
|
C | T | 1 | a0002c0011t0004g0181 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1064+1561C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288380 | ||||||
| chr13:31288405
|
A | G | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1064+1586A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288405 | ||||||
| chr13:31288754
|
C | T | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+1935C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288754 | ||||||
| chr13:31288806
|
A | C | 1 | a0001c0001t0024g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1064+1987A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288806 | ||||||
| chr13:31288872
|
A | G | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1064+2053A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288872 | ||||||
| chr13:31288893
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+2074A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288893 | ||||||
| chr13:31289104
|
T | C | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+2285T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289104 | ||||||
| chr13:31289183
|
A | T | 164 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(161): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1064+2364A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289183 | ||||||
| chr13:31289321
|
C | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+2502C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289321 | ||||||
| chr13:31289458
|
A | T | 1 | a0002c0002t0002g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1064+2639A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289458 | ||||||
| chr13:31289466
|
T | C | 240 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+2647T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289466 | ||||||
| chr13:31289536
|
T | C | 1 | a0002c0002t0002g0134 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1064+2717T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289536 | ||||||
| chr13:31289593
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+2774A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289593 | ||||||
| chr13:31289619
|
GA | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+2811delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31289619 | |||||
| chr13:31289866
|
GT | G | 5 | a0002c0002t0003g0009a0002c0002t0009g0013a0002c0002t0009g0210others(2): Show | 5 | HG02015.hp1 HG03209.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+3059delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31289866 | |||||
| chr13:31289870
|
T | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3051T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289870 | ||||||
| chr13:31290011
|
C | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3192C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290011 | ||||||
| chr13:31290116
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3297C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290116 | ||||||
| chr13:31290140
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1064+3321A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290140 | ||||||
| chr13:31290199
|
G | C | 250 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1064+3380G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290199 | ||||||
| chr13:31290470
|
A | G | 2 | a0002c0002t0002g0221a0002c0003t0021g0068 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1064+3651A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290470 | ||||||
| chr13:31290485
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3666G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290485 | ||||||
| chr13:31290589
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+3770T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290589 | ||||||
| chr13:31290672
|
C | T | 1 | a0002c0002t0004g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1064+3853C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290672 | ||||||
| chr13:31290682
|
C | A | 5 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | NA18942.hp1 NA18947.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+3863C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290682 | ||||||
| chr13:31290800
|
T | C | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+3981T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290800 | ||||||
| chr13:31290835
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1064+4016C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290835 | ||||||
| chr13:31290867
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+4048G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290867 | ||||||
| chr13:31290923
|
G | A | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1064+4104G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290923 | ||||||
| chr13:31290949
|
G | T | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1064+4130G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290949 | ||||||
| chr13:31291201
|
T | C | 1 | a0001c0001t0007g0028 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1064+4382T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291201 | ||||||
| chr13:31291346
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1064+4527T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291346 | ||||||
| chr13:31291681
|
T | C | 3 | a0004c0005t0001g0072a0004c0005t0001g0073a0004c0005t0001g0074 | 3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1064+4862T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291681 | ||||||
| chr13:31291693
|
T | C | 3 | a0004c0005t0001g0072a0004c0005t0001g0073a0004c0005t0001g0074 | 3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1064+4874T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291693 | ||||||
| chr13:31291859
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1064+5040G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291859 | ||||||
| chr13:31291877
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+5058A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291877 | ||||||
| chr13:31292041
|
T | C | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1064+5222T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292041 | ||||||
| chr13:31292141
|
G | A | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1064+5322G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292141 | ||||||
| chr13:31292182
|
C | T | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+5363C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292182 | ||||||
| chr13:31292208
|
T | G | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+5389T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292208 | ||||||
| chr13:31292246
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1064+5427G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292246 | ||||||
| chr13:31292449
|
T | C | 1 | a0001c0001t0005g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1064+5630T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292449 | ||||||
| chr13:31292699
|
C | CT | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1064+5890dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31292699 | |||||
| chr13:31292804
|
C | G | 1 | a0002c0002t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1064+5985C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292804 | ||||||
| chr13:31292816
|
T | TG | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+5998dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31292816 | |||||
| chr13:31292883
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0231 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1064+6064T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292883 | ||||||
| chr13:31292893
|
G | C | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+6074G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292893 | ||||||
| chr13:31293034
|
A | C | 8 | a0002c0002t0003g0002a0002c0002t0003g0067a0002c0002t0003g0088others(5): Show | 9 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1064+6215A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293034 | ||||||
| chr13:31293055
|
A | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+6236A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293055 | ||||||
| chr13:31293110
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+6291G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293110 | ||||||
| chr13:31293171
|
T | C | 2 | a0001c0001t0004g0032a0001c0001t0004g0173 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1064+6352T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293171 | ||||||
| chr13:31293441
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+6622T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293441 | ||||||
| chr13:31293487
|
G | A | 1 | a0002c0003t0002g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1064+6668G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293487 | ||||||
| chr13:31293557
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0217 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1064+6738G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293557 | ||||||
| chr13:31293693
|
G | GGGTGTCT others(39): Show |
1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+6877_1064+692 others(50): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31293693 | |||||
| chr13:31293902
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+7083C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293902 | ||||||
| chr13:31294273
|
T | G | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1064+7454T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294273 | ||||||
| chr13:31294307
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1064+7488T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294307 | ||||||
| chr13:31294457
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1064+7638T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294457 | ||||||
| chr13:31294769
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064+7950G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294769 | ||||||
| chr13:31294987
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+8168T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294987 | ||||||
| chr13:31295007
|
C | CT | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+8197dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31295007 | |||||
| chr13:31295017
|
G | T | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+8198G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295017 | ||||||
| chr13:31295089
|
C | T | 7 | a0002c0002t0003g0012a0002c0002t0003g0079a0002c0002t0003g0243others(4): Show | 7 | HG01255.hp1 HG01358.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1064+8270C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295089 | ||||||
| chr13:31295090
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+8271G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295090 | ||||||
| chr13:31295139
|
T | C | 1 | a0002c0002t0003g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1064+8320T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295139 | ||||||
| chr13:31295209
|
G | A | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1064+8390G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295209 | ||||||
| chr13:31295301
|
C | G | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1064+8482C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295301 | ||||||
| chr13:31295337
|
A | C | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1064+8518A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295337 | ||||||
| chr13:31295442
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+8623C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295442 | ||||||
| chr13:31295485
|
T | G | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1064+8666T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295485 | ||||||
| chr13:31295571
|
G | T | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1064+8752G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295571 | ||||||
| chr13:31295654
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+8835T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295654 | ||||||
| chr13:31295675
|
C | T | 1 | a0002c0002t0002g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1064+8856C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295675 | ||||||
| chr13:31295886
|
A | G | 246 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1064+9067A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295886 | ||||||
| chr13:31295988
|
G | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+9169G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295988 | ||||||
| chr13:31296075
|
C | T | 5 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0002t0002g0179others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064+9256C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296075 | ||||||
| chr13:31296092
|
C | G | 1 | a0002c0003t0002g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1064+9273C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296092 | ||||||
| chr13:31296135
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+9316G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296135 | ||||||
| chr13:31296257
|
G | A | 67 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(64): Show | 68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1064+9438G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296257 | ||||||
| chr13:31296377
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+9558C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296377 | ||||||
| chr13:31296493
|
G | A | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1064+9674G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296493 | ||||||
| chr13:31296702
|
CA | C | 5 | a0002c0002t0003g0031a0002c0002t0003g0033a0002c0002t0003g0220others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+9884delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296702 | ||||||
| chr13:31296703
|
AT | A | 240 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+9894delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31296703 | |||||
| chr13:31296750
|
C | A | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+9931C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296750 | ||||||
| chr13:31296785
|
T | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+9966T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296785 | ||||||
| chr13:31296812
|
A | G | 3 | a0002c0002t0002g0087a0002c0002t0002g0095a0002c0002t0002g0216 | 3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+9993A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296812 | ||||||
| chr13:31296956
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+10137A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296956 | ||||||
| chr13:31297025
|
G | GT | 71 | a0001c0001t0001g0089a0001c0001t0001g0187a0001c0001t0006g0042others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1064+10218dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297025 | |||||
| chr13:31297085
|
G | A | 3 | a0002c0002t0002g0087a0002c0002t0002g0095a0002c0002t0002g0216 | 3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+10266G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297085 | ||||||
| chr13:31297375
|
G | GT | 29 | a0001c0001t0001g0086a0001c0001t0001g0103a0001c0001t0001g0108others(26): Show | 29 | HG01074.hp2 HG01106.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.1064+10575dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | |||||
| chr13:31297375
|
GT | G | 38 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0062others(35): Show | 38 | HG00639.hp1 HG01071.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1064+10575delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | |||||
| chr13:31297375
|
GTT | G | 6 | a0001c0001t0001g0069a0001c0001t0001g0122a0001c0001t0001g0231others(3): Show | 6 | HG03098.hp2 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064+10574_1064+10 others(8): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | |||||
| chr13:31297375
|
GTTTT | G | 5 | a0002c0002t0002g0235a0002c0002t0002g0266a0002c0002t0009g0013others(2): Show | 5 | HG02109.hp1 HG03041.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+10572_1064+10 others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | |||||
| chr13:31297382
|
T | G | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1064+10563T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297382 | ||||||
| chr13:31297465
|
C | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+10646C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297465 | ||||||
| chr13:31297526
|
G | A | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1064+10707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297526 | ||||||
| chr13:31297576
|
A | G | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+10757A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297576 | ||||||
| chr13:31297664
|
A | C | 8 | a0002c0002t0003g0002a0002c0002t0003g0067a0002c0002t0003g0088others(5): Show | 9 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1064+10845A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297664 | ||||||
| chr13:31297832
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11013T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297832 | ||||||
| chr13:31297894
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064+11075G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297894 | ||||||
| chr13:31298044
|
A | C | 49 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0128others(46): Show | 49 | HG00558.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1064+11225A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298044 | ||||||
| chr13:31298068
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+11249C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298068 | ||||||
| chr13:31298069
|
C | A | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1064+11250C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298069 | ||||||
| chr13:31298127
|
C | T | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1064+11308C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298127 | ||||||
| chr13:31298198
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11379G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298198 | ||||||
| chr13:31298267
|
C | T | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1064+11448C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298267 | ||||||
| chr13:31298282
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+11463T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298282 | ||||||
| chr13:31298377
|
T | G | 166 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1064+11558T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298377 | ||||||
| chr13:31298456
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0231 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1064+11637G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298456 | ||||||
| chr13:31298508
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11689G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298508 | ||||||
| chr13:31298621
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0242a0001c0001t0007g0028 | 3 | HG00140.hp1 HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1064+11802C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298621 | ||||||
| chr13:31298682
|
C | T | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+11863C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298682 | ||||||
| chr13:31298688
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11869G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298688 | ||||||
| chr13:31298689
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1064+11870G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298689 | ||||||
| chr13:31298728
|
T | C | 5 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(2): Show | 5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+11909T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298728 | ||||||
| chr13:31298793
|
T | G | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+11974T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298793 | ||||||
| chr13:31298834
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+12015G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298834 | ||||||
| chr13:31298984
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1064+12165C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298984 | ||||||
| chr13:31299249
|
G | A | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1064+12430G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299249 | ||||||
| chr13:31299367
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+12548C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299367 | ||||||
| chr13:31299410
|
G | A | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1064+12591G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299410 | ||||||
| chr13:31299492
|
T | C | 1 | a0002c0002t0003g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1064+12673T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299492 | ||||||
| chr13:31299679
|
C | T | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+12860C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299679 | ||||||
| chr13:31300086
|
C | G | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1064+13267C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300086 | ||||||
| chr13:31300158
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+13339G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300158 | ||||||
| chr13:31300166
|
C | T | 169 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1064+13347C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300166 | ||||||
| chr13:31300168
|
G | T | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+13349G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300168 | ||||||
| chr13:31300307
|
C | T | 170 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(167): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1064+13488C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300307 | ||||||
| chr13:31300370
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0150a0001c0001t0001g0152others(4): Show | 7 | HG01074.hp1 HG01952.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1064+13551C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300370 | ||||||
| chr13:31300380
|
T | C | 1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1064+13561T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300380 | ||||||
| chr13:31300718
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+13899C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300718 | ||||||
| chr13:31300779
|
T | A | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+13960T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300779 | ||||||
| chr13:31300856
|
G | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+14037G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300856 | ||||||
| chr13:31300917
|
G | A | 1 | a0002c0002t0008g0125 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1064+14098G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300917 | ||||||
| chr13:31300953
|
C | T | 1 | a0002c0002t0006g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1064+14134C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300953 | ||||||
| chr13:31301003
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14184C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301003 | ||||||
| chr13:31301325
|
C | T | 1 | a0002c0002t0003g0260 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1064+14506C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301325 | ||||||
| chr13:31301372
|
A | T | 265 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1064+14553A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301372 | ||||||
| chr13:31301465
|
C | T | 1 | a0001c0001t0025g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1064+14646C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301465 | ||||||
| chr13:31301509
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14690G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301509 | ||||||
| chr13:31301624
|
G | A | 4 | a0002c0003t0003g0026a0002c0003t0003g0228a0005c0006t0003g0226others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+14805G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301624 | ||||||
| chr13:31301633
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+14814C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301633 | ||||||
| chr13:31301668
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14849C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301668 | ||||||
| chr13:31302006
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+15187G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302006 | ||||||
| chr13:31302015
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+15196T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302015 | ||||||
| chr13:31302018
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+15199T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302018 | ||||||
| chr13:31302049
|
C | T | 1 | a0002c0002t0008g0143 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+15230C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302049 | ||||||
| chr13:31302075
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1064+15256C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302075 | ||||||
| chr13:31302234
|
C | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15332C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302234 | ||||||
| chr13:31302350
|
C | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-15216C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302350 | ||||||
| chr13:31302351
|
G | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15215G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302351 | ||||||
| chr13:31302374
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15192G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302374 | ||||||
| chr13:31302385
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15181C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302385 | ||||||
| chr13:31302386
|
G | A | 5 | a0002c0002t0004g0081a0002c0002t0009g0013a0002c0002t0009g0210others(2): Show | 5 | HG02015.hp1 NA18963.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-15180G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302386 | ||||||
| chr13:31302451
|
C | T | 1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065-15115C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302451 | ||||||
| chr13:31302469
|
C | T | 67 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(64): Show | 68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1065-15097C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302469 | ||||||
| chr13:31302485
|
C | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-15081C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302485 | ||||||
| chr13:31302486
|
G | C | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-15080G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302486 | ||||||
| chr13:31302520
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-15046G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302520 | ||||||
| chr13:31302647
|
G | A | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1065-14919G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302647 | ||||||
| chr13:31302692
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1065-14874G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302692 | ||||||
| chr13:31302733
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14833G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302733 | ||||||
| chr13:31302737
|
A | G | 61 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1065-14829A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302737 | ||||||
| chr13:31302738
|
C | T | 1 | a0001c0001t0006g0056 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1065-14828C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302738 | ||||||
| chr13:31302740
|
G | A | 251 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1065-14826G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302740 | ||||||
| chr13:31302762
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14804C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302762 | ||||||
| chr13:31302799
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14767G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302799 | ||||||
| chr13:31302825
|
A | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14741A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302825 | ||||||
| chr13:31302881
|
GACAA | G | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-14679_1065-14 others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31302881 | |||||
| chr13:31302966
|
T | G | 170 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(167): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1065-14600T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302966 | ||||||
| chr13:31303012
|
C | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-14554C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303012 | ||||||
| chr13:31303032
|
C | T | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-14534C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303032 | ||||||
| chr13:31303081
|
T | C | 242 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1065-14485T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303081 | ||||||
| chr13:31303082
|
G | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14484G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303082 | ||||||
| chr13:31303091
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14475T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303091 | ||||||
| chr13:31303163
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-14403G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303163 | ||||||
| chr13:31303216
|
A | G | 1 | a0002c0002t0003g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1065-14350A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303216 | ||||||
| chr13:31303267
|
T | C | 5 | a0002c0002t0003g0238a0002c0002t0003g0245a0002c0002t0003g0247others(2): Show | 5 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-14299T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303267 | ||||||
| chr13:31303342
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14224G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303342 | ||||||
| chr13:31303364
|
C | T | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1065-14202C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303364 | ||||||
| chr13:31303462
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14104C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303462 | ||||||
| chr13:31303800
|
A | G | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1065-13766A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303800 | ||||||
| chr13:31303950
|
G | GA | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-13613dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31303950 | |||||
| chr13:31303951
|
A | G | 1 | a0002c0010t0003g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1065-13615A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303951 | ||||||
| chr13:31303971
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13595C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303971 | ||||||
| chr13:31303981
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13585G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303981 | ||||||
| chr13:31304023
|
G | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-13543G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304023 | ||||||
| chr13:31304146
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13420C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304146 | ||||||
| chr13:31304201
|
C | T | 74 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(71): Show | 75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1065-13365C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304201 | ||||||
| chr13:31304244
|
C | T | 1 | a0002c0002t0003g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1065-13322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304244 | ||||||
| chr13:31304348
|
T | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-13218T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304348 | ||||||
| chr13:31304416
|
C | G | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1065-13150C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304416 | ||||||
| chr13:31304591
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12975C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304591 | ||||||
| chr13:31304608
|
A | G | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12958A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304608 | ||||||
| chr13:31304625
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-12941T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304625 | ||||||
| chr13:31304688
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12878G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304688 | ||||||
| chr13:31304693
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12873C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304693 | ||||||
| chr13:31305013
|
G | C | 7 | a0002c0002t0001g0252a0002c0002t0003g0094a0002c0002t0003g0246others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-12553G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305013 | ||||||
| chr13:31305035
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-12531T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305035 | ||||||
| chr13:31305039
|
C | T | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12527C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305039 | ||||||
| chr13:31305130
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0231 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-12436C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305130 | ||||||
| chr13:31305262
|
A | C | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-12304A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305262 | ||||||
| chr13:31305338
|
T | C | 62 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1065-12228T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305338 | ||||||
| chr13:31305339
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12227G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305339 | ||||||
| chr13:31305339
|
G | T | 59 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0051others(56): Show | 59 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1065-12227G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305339 | ||||||
| chr13:31305378
|
A | G | 67 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(64): Show | 68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1065-12188A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305378 | ||||||
| chr13:31305405
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12161G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305405 | ||||||
| chr13:31305473
|
A | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-12093A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305473 | ||||||
| chr13:31305488
|
A | G | 75 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(72): Show | 76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1065-12078A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305488 | ||||||
| chr13:31305556
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-12010T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305556 | ||||||
| chr13:31305566
|
C | G | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1065-12000C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305566 | ||||||
| chr13:31305764
|
G | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11802G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305764 | ||||||
| chr13:31305782
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-11784C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305782 | ||||||
| chr13:31305783
|
T | G | 75 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(72): Show | 76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1065-11783T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305783 | ||||||
| chr13:31305824
|
T | G | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1065-11742T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305824 | ||||||
| chr13:31305859
|
G | A | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-11707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305859 | ||||||
| chr13:31305916
|
T | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-11650T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305916 | ||||||
| chr13:31305955
|
G | A | 1 | a0002c0002t0002g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1065-11611G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305955 | ||||||
| chr13:31305980
|
C | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11586C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305980 | ||||||
| chr13:31306100
|
G | T | 1 | a0001c0001t0005g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1065-11466G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306100 | ||||||
| chr13:31306127
|
C | G | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1065-11439C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306127 | ||||||
| chr13:31306131
|
C | G | 75 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(72): Show | 76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1065-11435C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306131 | ||||||
| chr13:31306282
|
C | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11284C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306282 | ||||||
| chr13:31306293
|
C | T | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1065-11273C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306293 | ||||||
| chr13:31306300
|
A | C | 7 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(4): Show | 7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-11266A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306300 | ||||||
| chr13:31306310
|
C | G | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-11256C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306310 | ||||||
| chr13:31306366
|
A | G | 1 | a0002c0003t0002g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1065-11200A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306366 | ||||||
| chr13:31306430
|
C | T | 1 | a0001c0001t0005g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1065-11136C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306430 | ||||||
| chr13:31306436
|
G | A | 1 | a0001c0001t0004g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1065-11130G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306436 | ||||||
| chr13:31306478
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-11088G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306478 | ||||||
| chr13:31306544
|
A | AATCAT | 8 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11022_1065-11 others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306544 | ||||||
| chr13:31306545
|
C | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11021C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306545 | ||||||
| chr13:31306551
|
G | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11015G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306551 | ||||||
| chr13:31306570
|
C | G | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-10996C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306570 | ||||||
| chr13:31306583
|
A | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-10983A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306583 | ||||||
| chr13:31306612
|
C | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-10954C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306612 | ||||||
| chr13:31306673
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10893A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306673 | ||||||
| chr13:31306686
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-10880T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306686 | ||||||
| chr13:31306735
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10831C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306735 | ||||||
| chr13:31306768
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1065-10798C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306768 | ||||||
| chr13:31306858
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10708G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306858 | ||||||
| chr13:31306868
|
G | A | 1 | a0002c0002t0002g0233 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1065-10698G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306868 | ||||||
| chr13:31306879
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10687C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306879 | ||||||
| chr13:31306999
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-10567C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306999 | ||||||
| chr13:31307098
|
C | T | 5 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0002t0002g0179others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-10468C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307098 | ||||||
| chr13:31307158
|
T | C | 3 | a0002c0003t0003g0026a0005c0006t0003g0226a0005c0006t0003g0227 | 3 | HG01256.hp2 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1065-10408T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307158 | ||||||
| chr13:31307167
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1065-10399T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307167 | ||||||
| chr13:31307208
|
G | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-10358G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307208 | ||||||
| chr13:31307315
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10251G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307315 | ||||||
| chr13:31307319
|
A | G | 1 | a0001c0001t0004g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-10247A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307319 | ||||||
| chr13:31307338
|
A | C | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-10228A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307338 | ||||||
| chr13:31307343
|
A | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0231 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-10223A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307343 | ||||||
| chr13:31307347
|
C | A | 3 | a0001c0001t0001g0184a0002c0002t0003g0240a0002c0002t0018g0253 | 3 | HG01496.hp2 HG03130.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1065-10219C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307347 | ||||||
| chr13:31307411
|
A | G | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-10155A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307411 | ||||||
| chr13:31307420
|
G | A | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1065-10146G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307420 | ||||||
| chr13:31307433
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1065-10133C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307433 | ||||||
| chr13:31307498
|
A | C | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1065-10068A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307498 | ||||||
| chr13:31307509
|
A | C | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-10057A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307509 | ||||||
| chr13:31307614
|
A | T | 5 | a0002c0002t0002g0064a0002c0002t0002g0065a0002c0002t0002g0179others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-9952A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307614 | ||||||
| chr13:31307712
|
G | A | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9854G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307712 | ||||||
| chr13:31307727
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-9839G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307727 | ||||||
| chr13:31307757
|
T | G | 1 | a0002c0002t0002g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1065-9809T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307757 | ||||||
| chr13:31307765
|
T | A | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9801T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307765 | ||||||
| chr13:31307767
|
A | G | 145 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1065-9799A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307767 | ||||||
| chr13:31307779
|
C | A | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9787C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307779 | ||||||
| chr13:31307779
|
C | T | 1 | a0002c0002t0003g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1065-9787C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307779 | ||||||
| chr13:31307788
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-9778T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307788 | ||||||
| chr13:31307867
|
G | A | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9699G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307867 | ||||||
| chr13:31307874
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1065-9692C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307874 | ||||||
| chr13:31307883
|
G | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-9683G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307883 | ||||||
| chr13:31307883
|
G | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9683G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307883 | ||||||
| chr13:31307895
|
C | T | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1065-9671C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307895 | ||||||
| chr13:31307902
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(1): Show | 4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9664A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307902 | ||||||
| chr13:31307926
|
C | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-9640C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307926 | ||||||
| chr13:31308015
|
A | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9551A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308015 | ||||||
| chr13:31308098
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9468C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308098 | ||||||
| chr13:31308131
|
A | G | 162 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1065-9435A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308131 | ||||||
| chr13:31308173
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9393T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308173 | ||||||
| chr13:31308176
|
C | A | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1065-9390C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308176 | ||||||
| chr13:31308176
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9390C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308176 | ||||||
| chr13:31308179
|
T | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(1): Show | 4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9387T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308179 | ||||||
| chr13:31308188
|
C | G | 5 | a0001c0001t0005g0200a0001c0001t0005g0202a0001c0001t0005g0206others(2): Show | 5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9378C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308188 | ||||||
| chr13:31308195
|
G | C | 5 | a0001c0001t0005g0200a0001c0001t0005g0202a0001c0001t0005g0206others(2): Show | 5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9371G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308195 | ||||||
| chr13:31308245
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9321G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308245 | ||||||
| chr13:31308313
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9253C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308313 | ||||||
| chr13:31308331
|
A | ATAAAAAA others(7): Show |
1 | a0001c0001t0001g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1065-9223_1065-922 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308331 | |||||
| chr13:31308332
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0015g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1065-9223_1065-922 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308332 | |||||
| chr13:31308332
|
TA | T | 18 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(15): Show | 18 | HG00639.hp1 HG02015.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1065-9221delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308332 | |||||
| chr13:31308333
|
A | AAAAAAAA others(6): Show |
6 | a0001c0001t0001g0086a0001c0001t0001g0175a0001c0001t0001g0178others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308333 | |||||
| chr13:31308334
|
A | AAAAAAAA others(5): Show |
26 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0217others(23): Show | 26 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308334 | |||||
| chr13:31308335
|
A | AAAAAAAA others(4): Show |
7 | a0001c0001t0001g0108a0001c0001t0004g0038a0001c0001t0004g0053others(4): Show | 7 | HG01943.hp1 HG02129.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308335 | |||||
| chr13:31308345
|
A | T | 174 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1065-9221A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308345 | ||||||
| chr13:31308346
|
T | A | 49 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0118others(46): Show | 49 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1065-9220T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308346 | ||||||
| chr13:31308347
|
T | A | 122 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0001g0108others(119): Show | 123 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1065-9219T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308347 | ||||||
| chr13:31308347
|
T | TA | 6 | a0002c0002t0004g0172a0002c0002t0004g0183a0002c0002t0012g0174others(3): Show | 6 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-9206dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | |||||
| chr13:31308347
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0232 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1065-9209_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | |||||
| chr13:31308347
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1065-9210_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | |||||
| chr13:31308347
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1065-9211_1065-921 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | |||||
| chr13:31308355
|
A | C | 1 | a0002c0002t0008g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1065-9211A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308355 | ||||||
| chr13:31308356
|
A | AACAAAAA others(1): Show |
66 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(63): Show | 67 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1065-9209_1065-920 others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308356 | |||||
| chr13:31308356
|
A | AACAAAAA others(7): Show |
4 | a0002c0003t0002g0162a0002c0003t0002g0171a0002c0007t0023g0004others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065-9209_1065-920 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308356 | |||||
| chr13:31308358
|
A | C | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9208A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308358 | ||||||
| chr13:31308361
|
C | A | 147 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(144): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1065-9205C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308361 | ||||||
| chr13:31308361
|
CA | C | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9195delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308361 | |||||
| chr13:31308362
|
A | AAAAAAAA others(6): Show |
81 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0046others(78): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1065-9195_1065-919 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAAAAAAA others(5): Show |
12 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0117others(9): Show | 12 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065-9195_1065-919 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1065-9195_1065-919 others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAAAAAAC others(6): Show |
1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1065-9198_1065-919 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAAAC | 70 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(67): Show | 71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065-9201_1065-920 others(8): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAACAAAA others(7): Show |
1 | a0001c0001t0010g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAACAAAA others(6): Show |
1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | AAACAAAA others(5): Show |
1 | a0002c0002t0002g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | |||||
| chr13:31308362
|
A | ACAAAAAC others(16): Show |
4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9204_1065-920 others(27): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308362 | ||||||
| chr13:31308362
|
A | C | 34 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0184others(31): Show | 34 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1065-9204A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308362 | ||||||
| chr13:31308414
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01074.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1065-9152A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308414 | ||||||
| chr13:31308441
|
T | C | 5 | a0001c0001t0005g0200a0001c0001t0005g0202a0001c0001t0005g0206others(2): Show | 5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9125T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308441 | ||||||
| chr13:31308647
|
A | G | 2 | a0002c0002t0012g0174a0002c0002t0012g0176 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1065-8919A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308647 | ||||||
| chr13:31308862
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(1): Show | 4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-8704C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308862 | ||||||
| chr13:31308875
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1065-8691C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308875 | ||||||
| chr13:31308907
|
G | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-8659G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308907 | ||||||
| chr13:31308933
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8633T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308933 | ||||||
| chr13:31308956
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8610G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308956 | ||||||
| chr13:31309028
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0231 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-8538G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309028 | ||||||
| chr13:31309037
|
A | T | 3 | a0001c0001t0004g0185a0001c0001t0004g0215a0001c0001t0004g0218 | 3 | HG02280.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1065-8529A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309037 | ||||||
| chr13:31309358
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8208C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309358 | ||||||
| chr13:31309396
|
C | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-8170C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309396 | ||||||
| chr13:31309466
|
C | T | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-8100C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309466 | ||||||
| chr13:31309488
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1065-8078G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309488 | ||||||
| chr13:31309560
|
C | T | 2 | a0002c0002t0003g0025a0002c0002t0017g0019 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1065-8006C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309560 | ||||||
| chr13:31309603
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7963T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309603 | ||||||
| chr13:31309654
|
T | C | 1 | a0002c0002t0003g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1065-7912T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309654 | ||||||
| chr13:31309678
|
T | A | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-7888T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309678 | ||||||
| chr13:31309694
|
C | T | 1 | a0002c0002t0002g0233 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1065-7872C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309694 | ||||||
| chr13:31309726
|
A | G | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-7840A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309726 | ||||||
| chr13:31309960
|
C | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0237 | 2 | HG03927.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1065-7606C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309960 | ||||||
| chr13:31310087
|
C | T | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-7479C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310087 | ||||||
| chr13:31310175
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1065-7391C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310175 | ||||||
| chr13:31310182
|
G | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-7384G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310182 | ||||||
| chr13:31310270
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7296G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310270 | ||||||
| chr13:31310525
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7041G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310525 | ||||||
| chr13:31310574
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6992C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310574 | ||||||
| chr13:31310685
|
A | T | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1065-6881A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310685 | ||||||
| chr13:31310780
|
G | A | 1 | a0001c0001t0005g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1065-6786G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310780 | ||||||
| chr13:31310944
|
G | A | 1 | a0001c0001t0015g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1065-6622G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310944 | ||||||
| chr13:31311016
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6550C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311016 | ||||||
| chr13:31311017
|
G | A | 166 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1065-6549G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311017 | ||||||
| chr13:31311029
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6537A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311029 | ||||||
| chr13:31311055
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6511C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311055 | ||||||
| chr13:31311078
|
T | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6488T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311078 | ||||||
| chr13:31311112
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-6454T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311112 | ||||||
| chr13:31311381
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1065-6185G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311381 | ||||||
| chr13:31311467
|
T | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-6099T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311467 | ||||||
| chr13:31311687
|
C | T | 2 | a0002c0002t0003g0240a0002c0003t0003g0188 | 2 | HG01496.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1065-5879C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311687 | ||||||
| chr13:31311746
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5820A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311746 | ||||||
| chr13:31311770
|
A | G | 70 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(67): Show | 71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065-5796A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311770 | ||||||
| chr13:31312040
|
A | G | 4 | a0002c0002t0003g0238a0002c0002t0003g0245a0002c0002t0003g0247others(1): Show | 4 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-5526A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312040 | ||||||
| chr13:31312092
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5474G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312092 | ||||||
| chr13:31312107
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1065-5459G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312107 | ||||||
| chr13:31312166
|
A | G | 1 | a0001c0001t0004g0185 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1065-5400A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312166 | ||||||
| chr13:31312222
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5344C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312222 | ||||||
| chr13:31312365
|
A | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0175others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-5201A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312365 | ||||||
| chr13:31312469
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5097T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312469 | ||||||
| chr13:31312677
|
G | A | 1 | a0001c0001t0005g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1065-4889G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312677 | ||||||
| chr13:31312713
|
A | G | 72 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(69): Show | 73 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1065-4853A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312713 | ||||||
| chr13:31312772
|
A | G | 1 | a0002c0003t0002g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1065-4794A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312772 | ||||||
| chr13:31312901
|
C | T | 1 | a0002c0002t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1065-4665C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312901 | ||||||
| chr13:31312930
|
C | T | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-4636C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312930 | ||||||
| chr13:31313084
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-4482T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313084 | ||||||
| chr13:31313096
|
G | A | 1 | a0002c0002t0003g0094 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1065-4470G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313096 | ||||||
| chr13:31313225
|
G | C | 1 | a0002c0002t0003g0241 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1065-4341G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313225 | ||||||
| chr13:31313450
|
G | C | 1 | a0002c0002t0008g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1065-4116G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313450 | ||||||
| chr13:31313537
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-4029A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313537 | ||||||
| chr13:31313704
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-3862G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313704 | ||||||
| chr13:31313771
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1065-3795A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313771 | ||||||
| chr13:31313889
|
G | A | 1 | a0002c0002t0002g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1065-3677G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313889 | ||||||
| chr13:31313997
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-3569G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313997 | ||||||
| chr13:31314022
|
C | T | 1 | a0002c0002t0003g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-3544C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314022 | ||||||
| chr13:31314190
|
A | G | 239 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1065-3376A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314190 | ||||||
| chr13:31314359
|
G | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-3207G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314359 | ||||||
| chr13:31314465
|
G | A | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-3101G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314465 | ||||||
| chr13:31314630
|
G | A | 69 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(66): Show | 70 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1065-2936G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314630 | ||||||
| chr13:31314803
|
C | T | 1 | a0007c0009t0002g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1065-2763C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314803 | ||||||
| chr13:31314903
|
G | A | 67 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(64): Show | 68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1065-2663G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314903 | ||||||
| chr13:31314963
|
C | T | 1 | a0002c0002t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-2603C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314963 | ||||||
| chr13:31315082
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1065-2484C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315082 | ||||||
| chr13:31315197
|
A | C | 1 | a0002c0002t0002g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1065-2369A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315197 | ||||||
| chr13:31315211
|
T | G | 1 | a0001c0001t0004g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-2355T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315211 | ||||||
| chr13:31315295
|
A | T | 251 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1065-2271A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315295 | ||||||
| chr13:31315368
|
G | A | 15 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(12): Show | 15 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1065-2198G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315368 | ||||||
| chr13:31315389
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-2177T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315389 | ||||||
| chr13:31315626
|
T | C | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-1940T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315626 | ||||||
| chr13:31315688
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-1878T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315688 | ||||||
| chr13:31315806
|
G | A | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-1760G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315806 | ||||||
| chr13:31315939
|
A | G | 237 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1065-1627A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315939 | ||||||
| chr13:31316259
|
C | T | 1 | a0002c0003t0002g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1065-1307C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316259 | ||||||
| chr13:31316405
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1065-1160_1065-115 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316405 | |||||
| chr13:31316407
|
T | A | 1 | a0001c0001t0004g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1065-1159T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | ||||||
| chr13:31316407
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | ||||||
| chr13:31316407
|
T | TATATATA others(10): Show |
2 | a0001c0001t0001g0118a0001c0001t0007g0149 | 2 | HG01192.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1065-1159_1065-115 others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | ||||||
| chr13:31316407
|
T | TATATATA others(18): Show |
1 | a0003c0004t0004g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(29): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | ||||||
| chr13:31316407
|
T | TATATATA others(28): Show |
1 | a0001c0001t0001g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(39): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | ||||||
| chr13:31316407
|
T | TTA | 6 | a0001c0001t0005g0104a0002c0002t0004g0023a0002c0002t0004g0172others(3): Show | 6 | HG01106.hp2 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-1136_1065-113 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(3): Show |
1 | a0002c0003t0003g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1065-1144_1065-113 others(14): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(5): Show |
1 | a0002c0003t0021g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065-1146_1065-113 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0178a0002c0002t0011g0006 | 3 | HG02280.hp1 NA18990.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1065-1148_1065-113 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(9): Show |
21 | a0001c0001t0001g0051a0001c0001t0001g0080a0001c0001t0001g0117others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1065-1150_1065-113 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(11): Show |
10 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0043others(7): Show | 10 | HG01123.hp2 HG02015.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1065-1152_1065-113 others(22): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(13): Show |
9 | a0001c0001t0001g0055a0001c0001t0001g0084a0001c0001t0001g0089others(6): Show | 9 | HG00735.hp1 HG01167.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065-1154_1065-113 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(15): Show |
9 | a0001c0001t0001g0062a0001c0001t0001g0070a0001c0001t0001g0113others(6): Show | 9 | HG00741.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065-1156_1065-113 others(26): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(17): Show |
12 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0108others(9): Show | 12 | HG00621.hp2 HG01074.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065-1158_1065-113 others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(19): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0085others(5): Show | 8 | HG00099.hp2 HG01071.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(30): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(21): Show |
8 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0001g0100others(5): Show | 8 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(32): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(23): Show |
8 | a0001c0001t0001g0076a0001c0001t0001g0193a0001c0001t0004g0041others(5): Show | 8 | HG00639.hp2 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(34): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(25): Show |
5 | a0001c0001t0005g0202a0001c0001t0007g0015a0001c0001t0007g0027others(2): Show | 5 | HG01361.hp1 HG02818.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(36): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(27): Show |
10 | a0001c0001t0001g0231a0001c0001t0005g0254a0001c0001t0007g0016others(7): Show | 10 | HG00738.hp1 HG01175.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(38): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(29): Show |
8 | a0001c0001t0001g0256a0001c0001t0005g0200a0001c0001t0007g0018others(5): Show | 8 | HG00140.hp2 HG00639.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(40): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(31): Show |
3 | a0001c0001t0004g0039a0001c0001t0005g0099a0001c0001t0005g0198 | 3 | HG02027.hp1 NA18612.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(42): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(44): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(35): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0115 | 2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(46): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(37): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0014g0186 | 3 | HG00140.hp1 HG01255.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(48): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(39): Show |
1 | a0002c0002t0002g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(50): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(54): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(3): Show |
9 | a0002c0002t0003g0002a0002c0002t0003g0088a0002c0002t0003g0238others(6): Show | 10 | HG00738.hp2 HG01123.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(14): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(5): Show |
16 | a0002c0002t0002g0017a0002c0002t0002g0116a0002c0002t0002g0139others(13): Show | 16 | HG00621.hp1 HG01516.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(7): Show |
24 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0130others(21): Show | 24 | HG00099.hp1 HG00609.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(9): Show |
5 | a0002c0002t0002g0064a0002c0002t0002g0137a0002c0002t0002g0144others(2): Show | 5 | HG02698.hp2 HG02886.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(11): Show |
6 | a0002c0002t0002g0065a0002c0002t0002g0132a0002c0002t0003g0244others(3): Show | 6 | HG01358.hp2 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(22): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(13): Show |
3 | a0002c0002t0003g0243a0002c0002t0003g0248a0002c0002t0003g0255 | 3 | HG01255.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
T | TTTTATAT others(15): Show |
1 | a0002c0002t0001g0252 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1065-1158_1065-115 others(26): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316407
|
TTA | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-1136_1065-113 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | |||||
| chr13:31316409
|
A | T | 1 | a0002c0002t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-1157A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316409 | ||||||
| chr13:31316431
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0004g0185a0001c0001t0004g0218 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0006g0052a0001c0001t0022g0050 | 2 | NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0004g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(23): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0004g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(25): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(16): Show |
1 | a0003c0004t0004g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(27): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(22): Show |
8 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0047others(5): Show | 8 | HG01071.hp2 HG02056.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(33): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(24): Show |
5 | a0001c0001t0004g0161a0001c0001t0006g0042a0001c0001t0006g0147others(2): Show | 5 | HG01361.hp2 HG01943.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(35): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(26): Show |
3 | a0001c0001t0004g0032a0001c0001t0004g0119a0001c0001t0004g0164 | 3 | HG03209.hp1 NA18522.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(37): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0006g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(39): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(30): Show |
4 | a0001c0001t0004g0120a0001c0001t0006g0049a0001c0001t0006g0169others(1): Show | 4 | NA18947.hp1 NA18952.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(41): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(32): Show |
3 | a0001c0001t0004g0163a0001c0001t0006g0054a0001c0001t0006g0057 | 3 | HG00558.hp1 HG03130.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(43): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0006g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(45): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316431
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0004g0061 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(49): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | ||||||
| chr13:31316432
|
A | T | 6 | a0001c0001t0001g0168a0001c0001t0004g0039a0001c0001t0004g0040others(3): Show | 6 | HG00673.hp1 HG01169.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-1134A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316432 | ||||||
| chr13:31316434
|
T | A | 35 | a0001c0001t0004g0032a0001c0001t0004g0037a0001c0001t0004g0038others(32): Show | 35 | HG00558.hp1 HG01071.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.1065-1132T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | ||||||
| chr13:31316434
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1065-1132_1065-113 others(29): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | ||||||
| chr13:31316434
|
T | TATATATA others(45): Show |
1 | a0001c0001t0004g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1065-1132_1065-113 others(56): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | ||||||
| chr13:31316435
|
T | A | 2 | a0001c0001t0004g0039a0001c0001t0004g0041 | 2 | HG02602.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1065-1131T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316435 | ||||||
| chr13:31316439
|
T | C | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-1127T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316439 | ||||||
| chr13:31316680
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-886T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316680 | ||||||
| chr13:31316718
|
A | T | 2 | a0002c0002t0003g0229a0002c0002t0003g0265 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-848A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316718 | ||||||
| chr13:31316777
|
C | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-789C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316777 | ||||||
| chr13:31317062
|
G | T | 1 | a0002c0002t0003g0009 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1065-504G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317062 | ||||||
| chr13:31317118
|
G | A | 1 | a0002c0003t0002g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1065-448G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317118 | ||||||
| chr13:31317424
|
T | C | 264 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1065-142T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317424 | ||||||
| chr13:31317892
|
T | TAAAAAAA others(138): Show |
1 | a0002c0002t0008g0083 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1184+213_1184+214i others(147): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | |||||
| chr13:31317892
|
T | TAAAAAAG others(136): Show |
55 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(52): Show | 55 | HG00099.hp1 HG00609.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.1184+223_1184+224i others(145): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | |||||
| chr13:31317892
|
T | TAAAAAAG others(137): Show |
10 | a0002c0002t0002g0065a0002c0002t0002g0116a0002c0002t0002g0138others(7): Show | 11 | HG00621.hp1 HG01123.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184+223_1184+224i others(146): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | |||||
| chr13:31317892
|
T | TAAAAAAG others(138): Show |
1 | a0002c0002t0003g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1184+223_1184+224i others(147): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | |||||
| chr13:31317933
|
G | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+248G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31317933 | ||||||
| chr13:31317977
|
G | GA | 80 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(77): Show | 81 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1184+302dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317977 | |||||
| chr13:31318030
|
T | C | 1 | a0001c0001t0004g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1184+345T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318030 | ||||||
| chr13:31318264
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1184+579G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318264 | ||||||
| chr13:31318271
|
CA | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+590delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31318271 | |||||
| chr13:31318311
|
G | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+626G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318311 | ||||||
| chr13:31318581
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+896C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318581 | ||||||
| chr13:31318719
|
A | AT | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1184+1035dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31318719 | |||||
| chr13:31318893
|
T | C | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1184+1208T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318893 | ||||||
| chr13:31318933
|
A | G | 3 | a0001c0001t0005g0200a0001c0001t0005g0202a0002c0002t0018g0253 | 3 | HG00140.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1184+1248A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318933 | ||||||
| chr13:31319046
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1184+1361A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319046 | ||||||
| chr13:31319070
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1385A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319070 | ||||||
| chr13:31319109
|
C | T | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1184+1424C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319109 | ||||||
| chr13:31319187
|
G | C | 18 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0005g0001others(15): Show | 19 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+1502G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319187 | ||||||
| chr13:31319245
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1560C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319245 | ||||||
| chr13:31319252
|
T | C | 13 | a0001c0001t0006g0042a0001c0001t0006g0048a0001c0001t0006g0049others(10): Show | 13 | HG00558.hp1 HG01943.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+1567T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319252 | ||||||
| chr13:31319364
|
G | C | 71 | a0002c0002t0001g0252a0002c0002t0002g0017a0002c0002t0002g0064others(68): Show | 72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1184+1679G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319364 | ||||||
| chr13:31319390
|
A | ATAAACTA others(9): Show |
146 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1184+1711_1184+171 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31319390 | |||||
| chr13:31319444
|
C | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1759C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319444 | ||||||
| chr13:31319628
|
A | G | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(2): Show | 5 | NA18950.hp2 NA18952.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1943A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319628 | ||||||
| chr13:31319644
|
T | C | 1 | a0002c0002t0002g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1184+1959T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319644 | ||||||
| chr13:31319821
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2136C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319821 | ||||||
| chr13:31319917
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2232C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319917 | ||||||
| chr13:31319918
|
T | C | 7 | a0002c0002t0004g0172a0002c0002t0004g0177a0002c0002t0004g0182others(4): Show | 7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+2233T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319918 | ||||||
| chr13:31320165
|
G | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2480G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320165 | ||||||
| chr13:31320378
|
C | T | 165 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1184+2693C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320378 | ||||||
| chr13:31320382
|
A | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2697A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320382 | ||||||
| chr13:31320439
|
C | T | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1184+2754C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320439 | ||||||
| chr13:31320577
|
G | A | 1 | a0001c0001t0007g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1184+2892G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320577 | ||||||
| chr13:31320608
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2923T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320608 | ||||||
| chr13:31320814
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0201 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1185-2937C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320814 | ||||||
| chr13:31320997
|
A | G | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1185-2754A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320997 | ||||||
| chr13:31321325
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-2426C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321325 | ||||||
| chr13:31321330
|
T | C | 1 | a0002c0010t0003g0010 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1185-2421T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321330 | ||||||
| chr13:31321490
|
T | C | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1185-2261T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321490 | ||||||
| chr13:31321682
|
C | T | 1 | a0002c0002t0002g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1185-2069C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321682 | ||||||
| chr13:31321693
|
T | C | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1185-2058T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321693 | ||||||
| chr13:31321838
|
AT | A | 241 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1185-1903delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31321838 | |||||
| chr13:31321947
|
T | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(2): Show | 5 | NA18950.hp2 NA18952.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-1804T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321947 | ||||||
| chr13:31321954
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-1797C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321954 | ||||||
| chr13:31321990
|
C | A | 1 | a0001c0001t0007g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1185-1761C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321990 | ||||||
| chr13:31322058
|
T | C | 1 | a0001c0001t0004g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1185-1693T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322058 | ||||||
| chr13:31322084
|
T | C | 1 | a0002c0002t0003g0245 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1185-1667T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322084 | ||||||
| chr13:31322644
|
A | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-1107A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322644 | ||||||
| chr13:31322680
|
A | G | 1 | a0002c0002t0004g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1185-1071A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322680 | ||||||
| chr13:31322685
|
C | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-1066C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322685 | ||||||
| chr13:31322841
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-910G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322841 | ||||||
| chr13:31322962
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1185-789G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322962 | ||||||
| chr13:31323177
|
A | G | 3 | a0001c0001t0004g0185a0001c0001t0004g0215a0001c0001t0004g0218 | 3 | HG02280.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1185-574A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323177 | ||||||
| chr13:31323245
|
T | C | 232 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1185-506T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323245 | ||||||
| chr13:31323257
|
A | G | 4 | a0002c0002t0004g0177a0002c0002t0004g0183a0002c0002t0012g0174others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-494A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323257 | ||||||
| chr13:31323356
|
T | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-395T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323356 | ||||||
| chr13:31323479
|
C | G | 1 | a0001c0001t0007g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1185-272C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323479 | ||||||
| chr13:31324108
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1329+213G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324108 | ||||||
| chr13:31324230
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+335A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324230 | ||||||
| chr13:31324231
|
A | G | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1329+336A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324231 | ||||||
| chr13:31324232
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+337T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324232 | ||||||
| chr13:31324234
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+339T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324234 | ||||||
| chr13:31324235
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+340A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324235 | ||||||
| chr13:31324236
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+341T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324236 | ||||||
| chr13:31324237
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+342A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324237 | ||||||
| chr13:31324238
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+343G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324238 | ||||||
| chr13:31324240
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+345A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324240 | ||||||
| chr13:31324241
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+346C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324241 | ||||||
| chr13:31324242
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+347T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324242 | ||||||
| chr13:31324243
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+348G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324243 | ||||||
| chr13:31324244
|
A | G | 68 | a0002c0002t0002g0017a0002c0002t0002g0064a0002c0002t0002g0065others(65): Show | 69 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1329+349A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324244 | ||||||
| chr13:31324245
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+350C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324245 | ||||||
| chr13:31324246
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+351C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324246 | ||||||
| chr13:31324273
|
C | G | 3 | a0002c0002t0003g0031a0002c0002t0003g0033a0002c0002t0003g0257 | 3 | HG02717.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1329+378C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324273 | ||||||
| chr13:31324344
|
C | T | 1 | a0002c0002t0002g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1329+449C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324344 | ||||||
| chr13:31324374
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+479G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324374 | ||||||
| chr13:31324444
|
C | T | 232 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1329+549C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324444 | ||||||
| chr13:31324451
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+556C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324451 | ||||||
| chr13:31324543
|
C | T | 1 | a0002c0002t0002g0134 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1329+648C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324543 | ||||||
| chr13:31324568
|
A | G | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1329+673A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324568 | ||||||
| chr13:31324701
|
CT | C | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+813delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31324701 | |||||
| chr13:31324850
|
G | A | 14 | a0002c0002t0002g0029a0002c0002t0002g0030a0002c0002t0002g0082others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1329+955G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324850 | ||||||
| chr13:31324861
|
T | C | 2 | a0002c0002t0012g0174a0002c0002t0012g0176 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1329+966T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324861 | ||||||
| chr13:31324886
|
T | G | 1 | a0002c0002t0002g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1329+991T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324886 | ||||||
| chr13:31324895
|
G | A | 2 | a0002c0002t0002g0064a0002c0002t0002g0065 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1329+1000G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324895 | ||||||
| chr13:31324897
|
G | A | 4 | a0002c0003t0003g0026a0002c0003t0003g0228a0005c0006t0003g0226others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1002G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324897 | ||||||
| chr13:31324922
|
G | T | 4 | a0002c0002t0009g0013a0002c0002t0009g0210a0002c0002t0009g0211others(1): Show | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1027G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324922 | ||||||
| chr13:31324958
|
C | T | 2 | a0001c0001t0005g0203a0001c0001t0005g0204 | 2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1329+1063C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324958 | ||||||
| chr13:31325088
|
T | C | 3 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0230 | 3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1329+1193T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325088 | ||||||
| chr13:31325196
|
A | G | 1 | a0002c0002t0006g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1329+1301A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325196 | ||||||
| chr13:31325227
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | NA18983.hp1 NA18990.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+1332G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325227 | ||||||
| chr13:31325333
|
C | G | 1 | a0002c0002t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1329+1438C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325333 | ||||||
| chr13:31325465
|
C | G | 151 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(148): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1329+1570C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325465 | ||||||
| chr13:31326090
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+2195G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326090 | ||||||
| chr13:31326108
|
G | A | 213 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1329+2213G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326108 | ||||||
| chr13:31326156
|
T | A | 1 | a0002c0002t0003g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1329+2261T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326156 | ||||||
| chr13:31326275
|
C | CT | 172 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(169): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1329+2406dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31326275 | |||||
| chr13:31326275
|
C | CTT | 33 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0092others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1329+2405_1329+240 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31326275 | |||||
| chr13:31326483
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+2588G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326483 | ||||||
| chr13:31326498
|
G | A | 1 | a0002c0002t0003g0244 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1329+2603G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326498 | ||||||
| chr13:31326532
|
C | T | 2 | a0002c0002t0003g0025a0002c0002t0017g0019 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1329+2637C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326532 | ||||||
| chr13:31326900
|
C | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2601C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326900 | ||||||
| chr13:31326931
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2570T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326931 | ||||||
| chr13:31327068
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1330-2433T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327068 | ||||||
| chr13:31327073
|
C | A | 223 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(220): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1330-2428C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327073 | ||||||
| chr13:31327104
|
C | A | 213 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1330-2397C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327104 | ||||||
| chr13:31327365
|
T | G | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2136T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327365 | ||||||
| chr13:31327625
|
G | A | 3 | a0002c0002t0011g0005a0002c0002t0011g0006a0002c0002t0011g0007 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1330-1876G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327625 | ||||||
| chr13:31327631
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1330-1870G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327631 | ||||||
| chr13:31327696
|
G | A | 2 | a0002c0002t0002g0235a0002c0002t0002g0266 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1330-1805G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327696 | ||||||
| chr13:31327721
|
A | G | 209 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(206): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1330-1780A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327721 | ||||||
| chr13:31327899
|
C | T | 2 | a0002c0003t0002g0162a0002c0003t0002g0171 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1330-1602C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327899 | ||||||
| chr13:31327905
|
T | C | 15 | a0001c0001t0005g0001a0001c0001t0005g0045a0001c0001t0005g0066others(12): Show | 16 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1330-1596T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327905 | ||||||
| chr13:31327992
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-1509G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327992 | ||||||
| chr13:31328286
|
A | T | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-1215A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328286 | ||||||
| chr13:31328398
|
T | G | 209 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(206): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1330-1103T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328398 | ||||||
| chr13:31328524
|
G | A | 3 | a0003c0004t0004g0205a0003c0004t0004g0208a0003c0004t0004g0209 | 3 | HG01071.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1330-977G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328524 | ||||||
| chr13:31328690
|
C | T | 1 | a0002c0002t0003g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1330-811C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328690 | ||||||
| chr13:31328692
|
C | CA | 170 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0024others(167): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1330-784dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | |||||
| chr13:31328692
|
C | CAA | 33 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0102others(30): Show | 33 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1330-785_1330-784d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | |||||
| chr13:31328692
|
C | CAAA | 8 | a0001c0001t0001g0103a0001c0001t0005g0099a0002c0002t0003g0265others(5): Show | 8 | HG02074.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1330-786_1330-784d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | |||||
| chr13:31328717
|
A | C | 2 | a0002c0002t0009g0210a0002c0002t0009g0211 | 2 | HG02015.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1330-784A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328717 | ||||||
| chr13:31328760
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1330-741A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328760 | ||||||
| chr13:31328764
|
G | A | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-737G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328764 | ||||||
| chr13:31328847
|
A | G | 3 | a0002c0002t0004g0172a0002c0002t0004g0182a0002c0011t0004g0181 | 3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1330-654A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328847 | ||||||
| chr13:31328885
|
A | G | 3 | a0002c0002t0003g0031a0002c0002t0003g0033a0002c0002t0003g0257 | 3 | HG02717.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1330-616A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328885 | ||||||
| chr13:31329075
|
A | G | 1 | a0002c0002t0004g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1330-426A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329075 | ||||||
| chr13:31329116
|
A | C | 1 | a0002c0002t0018g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-385A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329116 | ||||||
| chr13:31329286
|
G | A | 1 | a0002c0007t0023g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1330-215G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329286 |