Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8848 |
|---|---|
| ensemblid | ENSG00000102804.16 |
| hgncid | 16826 |
| symbol | TSC22D1 |
| name | TSC22 domain family member 1 |
| refseq_nuc | NM_183422.4 |
| refseq_prot | NP_904358.2 |
| ensembl_nuc | ENST00000458659.3 |
| ensembl_prot | ENSP00000397435.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 44432143 |
| end | 44576330 |
| strand | - |
| ver | v1.2 |
| region | chr13:44432143-44576330 |
| region5000 | chr13:44427143-44581330 |
| regionname0 | TSC22D1_chr13_44432143_44576330 |
| regionname5000 | TSC22D1_chr13_44427143_44581330 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1073 | 214 | 53 | 42 | 87 | 8 | 22 | 65 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0002 | 0/0 | 1072 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0003 | 0/0 | 1072 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0004 | 0/0 | 1073 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0005 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0006 | 0/0 | 1073 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0007 | 0/0 | 1073 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0008 | 0/0 | 1073 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0009 | 0/0 | 1073 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0010 | 0/0 | 1073 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3222 | 205 | 48 | 42 | 86 | 8 | 19 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0002 | 0/0 | 3219 | 8 | 8 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0003 | 0/0 | 3219 | 6 | 0 | 6 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0004 | 0/0 | 3222 | 6 | 0 | 2 | 0 | 1 | 3 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0005 | 0/0 | 3222 | 4 | 4 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0006 | 0/0 | 3222 | 2 | 1 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0007 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0008 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0009 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0010 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0011 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0012 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0013 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0014 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| c0015 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2740 | 141 | 43 | 22 | 57 | 6 | 12 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0002 | 0/1 | 2741 | 61 | 6 | 20 | 25 | 2 | 7 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0003 | 0/0 | 2739 | 12 | 1 | 6 | 0 | 1 | 4 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0004 | 0/0 | 2739 | 4 | 4 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0005 | 0/0 | 2741 | 2 | 0 | 0 | 2 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0006 | 0/0 | 2739 | 2 | 1 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0007 | 0/0 | 2739 | 2 | 0 | 2 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0008 | 0/0 | 2740 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0009 | 0/0 | 2740 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0010 | 0/0 | 2741 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0011 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0012 | 0/0 | 2740 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0013 | 0/0 | 2740 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0014 | 0/0 | 2740 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0015 | 0/0 | 2741 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0016 | 0/0 | 2740 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0017 | 0/0 | 2740 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0018 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0019 | 0/0 | 2741 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0020 | 0/0 | 2741 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| t0021 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3222 | 205 | 48 | 42 | 86 | 8 | 19 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0005 | 0/0 | 3222 | 4 | 4 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0006 | 0/0 | 3222 | 2 | 1 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0010 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0014 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0015 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0002c0002 | 0/0 | 3219 | 8 | 8 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0003c0003 | 0/0 | 3219 | 6 | 0 | 6 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0004c0004 | 0/0 | 3222 | 6 | 0 | 2 | 0 | 1 | 3 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0005c0007 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0006c0011 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0007c0009 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0008c0013 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0009c0008 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0010c0012 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5961 | 130 | 34 | 22 | 57 | 5 | 11 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0002 | 0/1 | 5962 | 57 | 6 | 18 | 24 | 2 | 6 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0003 | 0/0 | 5960 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0004 | 0/0 | 5960 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0005 | 0/0 | 5962 | 2 | 0 | 0 | 2 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0006 | 0/0 | 5960 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0008 | 0/0 | 5961 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0010 | 0/0 | 5962 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0011 | 0/0 | 5960 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0012 | 0/0 | 5961 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0013 | 0/0 | 5961 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0014 | 0/0 | 5961 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0015 | 0/0 | 5962 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0016 | 0/0 | 5961 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0017 | 0/0 | 5961 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0018 | 0/0 | 5960 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0001t0019 | 0/0 | 5962 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0005t0004 | 0/0 | 5960 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0005t0009 | 0/0 | 5961 | 2 | 2 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0006t0006 | 0/0 | 5960 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0006t0021 | 0/0 | 5960 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0010t0002 | 0/0 | 5962 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0014t0003 | 0/0 | 5960 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0001c0015t0002 | 0/0 | 5962 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0002c0002t0001 | 0/0 | 5958 | 8 | 8 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0003c0003t0003 | 0/0 | 5957 | 6 | 0 | 6 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0004c0004t0001 | 0/0 | 5961 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0004c0004t0003 | 0/0 | 5960 | 3 | 0 | 0 | 0 | 0 | 3 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0004c0004t0007 | 0/0 | 5960 | 2 | 0 | 2 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0005c0007t0001 | 0/0 | 5961 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0006c0011t0002 | 0/0 | 5962 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0007c0009t0002 | 0/0 | 5962 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0008c0013t0003 | 0/0 | 5960 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0009c0008t0001 | 0/0 | 5961 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| a0010c0012t0020 | 0/0 | 5962 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | copy fasta | chr13 | 44427143 | 44581330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0011g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0014g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0017g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0001t0019g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0005t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0005t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0005t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0005t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0006t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0006t0021g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0010t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0014t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0001c0015t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0004c0004t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0005c0007t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0006c0011t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0007c0009t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0008c0013t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0009c0008t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| a0010c0012t0020g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00323 | hp1 | a0008 | c0013 | t0003 | g0222 | EUR | FIN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0063 | EUR | FIN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00733 | hp1 | a0004 | c0004 | t0007 | g0227 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00733 | hp2 | a0001 | c0001 | t0017 | g0066 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01167 | hp1 | a0007 | c0009 | t0002 | g0014 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0039 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01517 | hp1 | a0004 | c0004 | t0001 | g0225 | EUR | IBS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01928 | hp2 | a0003 | c0003 | t0003 | g0219 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01943 | hp2 | a0003 | c0003 | t0003 | g0221 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01978 | hp1 | a0006 | c0011 | t0002 | g0215 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01981 | hp1 | a0004 | c0004 | t0007 | g0228 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01993 | hp1 | a0003 | c0003 | t0003 | g0217 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02004 | hp2 | a0003 | c0003 | t0003 | g0218 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02132 | hp1 | a0001 | c0001 | t0016 | g0192 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02148 | hp2 | a0003 | c0003 | t0003 | g0220 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02273 | hp2 | a0003 | c0003 | t0003 | g0216 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02602 | hp2 | a0001 | c0010 | t0002 | g0214 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02647 | hp1 | a0001 | c0006 | t0021 | g0232 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02683 | hp2 | a0001 | c0001 | t0019 | g0138 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02735 | hp2 | a0001 | c0014 | t0003 | g0229 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02738 | hp2 | a0004 | c0004 | t0003 | g0224 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02922 | hp2 | a0001 | c0005 | t0009 | g0239 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0084 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0185 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0234 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03195 | hp2 | a0005 | c0007 | t0001 | g0012 | AFR | ESN | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0240 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03654 | hp2 | a0009 | c0008 | t0001 | g0013 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03704 | hp2 | a0004 | c0004 | t0003 | g0226 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03710 | hp1 | a0001 | c0006 | t0006 | g0003 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0077 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG04199 | hp1 | a0004 | c0004 | t0003 | g0223 | SAS | STU | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | YRI | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18948 | hp1 | a0010 | c0012 | t0020 | g0231 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18962 | hp1 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18964 | hp2 | a0001 | c0015 | t0002 | g0230 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19003 | hp2 | a0001 | c0001 | t0015 | g0152 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | LWK | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ASW | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | TSI | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG02559 | hp2 | a0001 | c0005 | t0009 | g0237 | AFR | ACB | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG03471 | hp2 | a0001 | c0005 | t0004 | g0238 | AFR | MSL | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | USA | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | USA | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | USA | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | LWK | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0113 | REF | REF | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | TSC22D1_chr13_44427143_44581330 | TSC22D1 | chr13 | 44427143 | 44581330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44573380
|
C | T | 1 | a0008 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.2695G>A | p.Ala899Thr | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 2951/5961 | 2695/3222 | 899/1073 | chr13 | 44573380 | ||
| chr13:44573763
|
C | T | 1 | a0007 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.2312G>A | p.Gly771Glu | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 2568/5961 | 2312/3222 | 771/1073 | chr13 | 44573763 | ||
| chr13:44574121
|
G | A | 3 | a0003a0004a0008 | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
missense_variant | MODERATE | c.1954C>T | p.Pro652Ser | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 2210/5961 | 1954/3222 | 652/1073 | chr13 | 44574121 | ||
| chr13:44574481
|
C | T | 1 | a0009 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1594G>A | p.Ala532Thr | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 1850/5961 | 1594/3222 | 532/1073 | chr13 | 44574481 | ||
| chr13:44574554
|
CTGT | C | 1 | a0002 | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
disruptive_inframe_deletion | MODERATE | c.1518_1520delACA | p.Gln507del | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 1776/5961 | 1518/3222 | 506/1073 | chr13 | 44574554 | ||
| chr13:44574729
|
TCCA | T | 1 | a0003 | 6 | HG01928.hp2 HG01943.hp2 HG01993.hp1 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.1343_1345delTGG | p.Val448del | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 1601/5961 | 1343/3222 | 448/1073 | chr13 | 44574729 | ||
| chr13:44574877
|
G | C | 1 | a0006 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1198C>G | p.Pro400Ala | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 1454/5961 | 1198/3222 | 400/1073 | chr13 | 44574877 | ||
| chr13:44575065
|
T | C | 1 | a0010 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.1010A>G | p.Asn337Ser | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 1266/5961 | 1010/3222 | 337/1073 | chr13 | 44575065 | ||
| chr13:44575616
|
C | G | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.459G>C | p.Glu153Asp | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 715/5961 | 459/3222 | 153/1073 | chr13 | 44575616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44573186
|
G | C | 1 | a0001c0010 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2889C>G | p.Pro963Pro | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 3145/5961 | 2889/3222 | 963/1073 | chr13 | 44573186 | ||
| chr13:44573957
|
T | C | 1 | a0001c0014 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.2118A>G | p.Ala706Ala | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 2374/5961 | 2118/3222 | 706/1073 | chr13 | 44573957 | ||
| chr13:44575526
|
G | A | 3 | a0003c0003a0004c0004a0008c0013 | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
synonymous_variant | LOW | c.549C>T | p.Ala183Ala | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 805/5961 | 549/3222 | 183/1073 | chr13 | 44575526 | ||
| chr13:44575559
|
G | A | 1 | a0001c0014 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.516C>T | p.Ser172Ser | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 772/5961 | 516/3222 | 172/1073 | chr13 | 44575559 | ||
| chr13:44575808
|
C | T | 2 | a0001c0006a0002c0002 | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
synonymous_variant | LOW | c.267G>A | p.Ser89Ser | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 523/5961 | 267/3222 | 89/1073 | chr13 | 44575808 | ||
| chr13:44575814
|
G | A | 1 | a0001c0005 | 4 | HG02559.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.261C>T | p.Leu87Leu | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 517/5961 | 261/3222 | 87/1073 | chr13 | 44575814 | ||
| chr13:44576069
|
G | A | 1 | a0001c0015 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.6C>T | p.His2His | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 262/5961 | 6/3222 | 2/1073 | chr13 | 44576069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44432327
|
G | A | 6 | a0001c0001t0003a0001c0014t0003a0003c0003t0003others(3): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2299C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 2299 | chr13 | 44432327 | |||||
| chr13:44432478
|
T | C | 1 | a0001c0001t0014 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2148A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 2148 | chr13 | 44432478 | |||||
| chr13:44432563
|
A | AG | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(7): Show | 67 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2062dupC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 2062 | chr13 | 44432563 | |||||
| chr13:44432640
|
A | T | 1 | a0001c0001t0013 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1986T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1986 | chr13 | 44432640 | |||||
| chr13:44432715
|
TA | T | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(10): Show | 23 | HG00323.hp1 HG00733.hp1 HG01192.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1910delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1910 | chr13 | 44432715 | |||||
| chr13:44432852
|
G | A | 1 | a0001c0001t0015 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1774 | chr13 | 44432852 | |||||
| chr13:44433230
|
G | A | 4 | a0001c0001t0004a0001c0001t0006a0001c0005t0004others(1): Show | 6 | HG02257.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1396C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1396 | chr13 | 44433230 | |||||
| chr13:44433261
|
A | G | 1 | a0001c0001t0012 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1365T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1365 | chr13 | 44433261 | |||||
| chr13:44433268
|
T | C | 1 | a0001c0001t0016 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1358 | chr13 | 44433268 | |||||
| chr13:44433339
|
T | C | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(10): Show | 23 | HG00323.hp1 HG00733.hp1 HG01192.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1287A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1287 | chr13 | 44433339 | |||||
| chr13:44433344
|
C | T | 2 | a0001c0001t0011a0001c0001t0018 | 2 | HG01192.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1282G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1282 | chr13 | 44433344 | |||||
| chr13:44433561
|
G | C | 1 | a0001c0001t0017 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 1065 | chr13 | 44433561 | |||||
| chr13:44434011
|
T | C | 1 | a0004c0004t0007 | 2 | HG00733.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*615A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 615 | chr13 | 44434011 | |||||
| chr13:44434154
|
C | G | 1 | a0001c0001t0010 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 472 | chr13 | 44434154 | |||||
| chr13:44434197
|
G | C | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(9): Show | 22 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*429C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 429 | chr13 | 44434197 | |||||
| chr13:44434439
|
G | A | 1 | a0001c0001t0019 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 187 | chr13 | 44434439 | |||||
| chr13:44434558
|
C | T | 1 | a0001c0001t0008 | 2 | HG02622.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*68G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 3/3 | 68 | chr13 | 44434558 | |||||
| chr13:44576136
|
G | C | 1 | a0010c0012t0020 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 62 | chr13 | 44576136 | |||||
| chr13:44576141
|
G | C | 1 | a0001c0006t0021 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 67 | chr13 | 44576141 | |||||
| chr13:44576150
|
G | A | 4 | a0001c0001t0004a0001c0001t0008a0001c0005t0004others(1): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-76C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | chr13 | 44576150 | ||||||
| chr13:44576220
|
C | G | 1 | a0001c0001t0005 | 2 | HG00558.hp1 HG02015.hp2 |
5_prime_UTR_variant | MODIFIER | c.-146G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/3 | 146 | chr13 | 44576220 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:44435056
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0081 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2965-173C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435056 | ||||||
| chr13:44435189
|
G | C | 2 | a0001c0001t0011g0039a0001c0001t0018g0084 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2965-306C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435189 | ||||||
| chr13:44435196
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2965-313A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435196 | ||||||
| chr13:44435396
|
C | A | 10 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(7): Show | 10 | HG00639.hp1 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.2965-513G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435396 | ||||||
| chr13:44435706
|
G | A | 6 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(3): Show | 6 | HG02257.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2964+338C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435706 | ||||||
| chr13:44435730
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2964+314G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435730 | ||||||
| chr13:44435792
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2964+252G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435792 | ||||||
| chr13:44435831
|
G | A | 2 | a0001c0001t0002g0144a0010c0012t0020g0231 | 2 | NA18948.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2964+213C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 2/2 | chr13 | 44435831 | ||||||
| chr13:44436147
|
T | G | 220 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2913-52A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436147 | ||||||
| chr13:44436414
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2913-319C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436414 | ||||||
| chr13:44436480
|
G | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-385C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436480 | ||||||
| chr13:44436484
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2913-389G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436484 | ||||||
| chr13:44436517
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2913-422A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436517 | ||||||
| chr13:44436668
|
G | C | 1 | a0001c0001t0002g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2913-573C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436668 | ||||||
| chr13:44436731
|
C | T | 22 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(19): Show | 22 | HG00323.hp1 HG00733.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2913-636G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436731 | ||||||
| chr13:44436919
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-824G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436919 | ||||||
| chr13:44436966
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0081 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2913-871A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436966 | ||||||
| chr13:44436974
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2913-879G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436974 | ||||||
| chr13:44436984
|
C | G | 2 | a0001c0001t0008g0233a0001c0001t0008g0234 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2913-889G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436984 | ||||||
| chr13:44436991
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2913-896T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44436991 | ||||||
| chr13:44437152
|
A | G | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-1057T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437152 | ||||||
| chr13:44437208
|
T | C | 26 | a0001c0001t0001g0106a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 26 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.2913-1113A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437208 | ||||||
| chr13:44437248
|
T | C | 22 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(19): Show | 22 | HG00323.hp1 HG00733.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2913-1153A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437248 | ||||||
| chr13:44437366
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2913-1271C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437366 | ||||||
| chr13:44437424
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2913-1329T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437424 | ||||||
| chr13:44437499
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2913-1404G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437499 | ||||||
| chr13:44437516
|
GAA | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-1423_2913-142 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437516 | ||||||
| chr13:44437563
|
C | T | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-1468G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437563 | ||||||
| chr13:44437612
|
C | T | 220 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2913-1517G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437612 | ||||||
| chr13:44437797
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2913-1702A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437797 | ||||||
| chr13:44437871
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2913-1776T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437871 | ||||||
| chr13:44437977
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2913-1882C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437977 | ||||||
| chr13:44437996
|
T | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-1901A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44437996 | ||||||
| chr13:44438054
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2913-1959T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438054 | ||||||
| chr13:44438055
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2913-1960A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438055 | ||||||
| chr13:44438472
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-2377C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438472 | ||||||
| chr13:44438476
|
T | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-2381A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438476 | ||||||
| chr13:44438729
|
C | CT | 7 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-2635dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438729 | ||||||
| chr13:44438772
|
T | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2913-2677A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438772 | ||||||
| chr13:44438983
|
A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG00597.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2913-2888T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44438983 | ||||||
| chr13:44439288
|
C | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-3193G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44439288 | ||||||
| chr13:44439468
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2913-3373C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44439468 | ||||||
| chr13:44439916
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2913-3821A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44439916 | ||||||
| chr13:44440290
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2913-4195A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44440290 | ||||||
| chr13:44440587
|
C | CA | 11 | a0001c0001t0001g0088a0001c0001t0001g0169a0001c0001t0001g0173others(8): Show | 11 | HG02056.hp1 HG02647.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2913-4493dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44440587 | ||||||
| chr13:44440587
|
CA | C | 86 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2913-4493delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44440587 | ||||||
| chr13:44441294
|
A | T | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-5199T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441294 | ||||||
| chr13:44441295
|
G | T | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2913-5200C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441295 | ||||||
| chr13:44441313
|
T | C | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-5218A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441313 | ||||||
| chr13:44441403
|
C | T | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-5308G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441403 | ||||||
| chr13:44441404
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2913-5309C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441404 | ||||||
| chr13:44441678
|
A | G | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-5583T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441678 | ||||||
| chr13:44441681
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2913-5586C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441681 | ||||||
| chr13:44441922
|
G | A | 68 | a0001c0001t0001g0088a0001c0001t0001g0182a0001c0001t0002g0015others(65): Show | 68 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2913-5827C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44441922 | ||||||
| chr13:44442125
|
A | C | 1 | a0001c0001t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2913-6030T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442125 | ||||||
| chr13:44442231
|
A | G | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-6136T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442231 | ||||||
| chr13:44442233
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0016g0192 | 2 | HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2913-6138T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442233 | ||||||
| chr13:44442311
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0090a0001c0001t0011g0039others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-6216A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442311 | ||||||
| chr13:44442766
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2913-6671T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442766 | ||||||
| chr13:44442775
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2913-6680G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442775 | ||||||
| chr13:44442843
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2913-6748T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442843 | ||||||
| chr13:44442865
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG00597.hp2 NA18941.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2913-6770G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442865 | ||||||
| chr13:44442903
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2913-6808G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442903 | ||||||
| chr13:44442914
|
C | CA | 81 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0034others(78): Show | 81 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2913-6820dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442914 | ||||||
| chr13:44442914
|
C | CAA | 108 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.2913-6821_2913-682 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442914 | ||||||
| chr13:44442914
|
C | CAAA | 9 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01070.hp2 HG01074.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2913-6822_2913-682 others(7): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44442914 | ||||||
| chr13:44443188
|
G | A | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2913-7093C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443188 | ||||||
| chr13:44443208
|
T | C | 211 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(208): Show | 211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.2913-7113A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443208 | ||||||
| chr13:44443209
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2913-7114C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443209 | ||||||
| chr13:44443309
|
G | GA | 40 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(37): Show | 40 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.2913-7215dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443309 | ||||||
| chr13:44443309
|
G | GAA | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-7216_2913-721 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443309 | ||||||
| chr13:44443475
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2913-7380G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443475 | ||||||
| chr13:44443546
|
A | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-7451T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443546 | ||||||
| chr13:44443875
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2913-7780C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443875 | ||||||
| chr13:44443960
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2913-7865A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44443960 | ||||||
| chr13:44444140
|
A | G | 5 | a0001c0001t0002g0133a0001c0001t0002g0135a0001c0001t0002g0136others(2): Show | 5 | HG01109.hp2 HG02273.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-8045T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444140 | ||||||
| chr13:44444141
|
T | C | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-8046A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444141 | ||||||
| chr13:44444278
|
C | CA | 10 | a0001c0001t0001g0029a0001c0001t0001g0091a0001c0001t0001g0092others(7): Show | 10 | HG02027.hp1 HG02083.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2913-8184dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444278
|
CA | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2913-8184delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444278
|
CAA | C | 84 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0042others(81): Show | 84 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2913-8185_2913-818 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444278
|
CAAA | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-8186_2913-818 others(7): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444278
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00597.hp2 NA18941.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-8193_2913-818 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444278
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0065 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2913-8196_2913-818 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444278 | ||||||
| chr13:44444308
|
AG | A | 3 | a0003c0003t0003g0217a0003c0003t0003g0218a0003c0003t0003g0221 | 3 | HG01943.hp2 HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2913-8214delC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444308 | ||||||
| chr13:44444309
|
G | A | 13 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-8214C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444309 | ||||||
| chr13:44444314
|
G | A | 16 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(13): Show | 16 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.2913-8219C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444314 | ||||||
| chr13:44444314
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2913-8219C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444314 | ||||||
| chr13:44444319
|
G | A | 9 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(6): Show | 9 | HG00323.hp1 HG01981.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2913-8224C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444319 | ||||||
| chr13:44444319
|
GA | G | 9 | a0001c0005t0004g0238a0001c0006t0006g0003a0003c0003t0003g0217others(6): Show | 9 | HG00733.hp1 HG01928.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2913-8225delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444319 | ||||||
| chr13:44444320
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0006g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2913-8226_2913-822 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444320 | ||||||
| chr13:44444320
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0004g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2913-8226_2913-822 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444320 | ||||||
| chr13:44444320
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0004g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2913-8226_2913-822 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444320 | ||||||
| chr13:44444320
|
A | G | 5 | a0003c0003t0003g0216a0004c0004t0003g0223a0004c0004t0003g0224others(2): Show | 5 | HG00323.hp1 HG01981.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-8225T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444320 | ||||||
| chr13:44444326
|
A | G | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-8231T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444326 | ||||||
| chr13:44444601
|
G | A | 7 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-8506C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444601 | ||||||
| chr13:44444775
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2913-8680C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444775 | ||||||
| chr13:44444874
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2913-8779T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44444874 | ||||||
| chr13:44445121
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2913-9026T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445121 | ||||||
| chr13:44445139
|
A | G | 212 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2913-9044T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445139 | ||||||
| chr13:44445216
|
T | TAC | 12 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0069others(9): Show | 12 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.2913-9123_2913-912 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
T | TACAC | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0096others(2): Show | 5 | HG02132.hp2 HG02622.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-9125_2913-912 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2913-9135_2913-912 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
TAC | T | 26 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(23): Show | 26 | HG00673.hp2 HG01243.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2913-9123_2913-912 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
TACAC | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0082 | 3 | HG00544.hp2 NA18960.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2913-9125_2913-912 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2913-9133_2913-912 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
TACACACA others(7): Show |
T | 5 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0174others(2): Show | 5 | HG01192.hp1 HG01975.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-9135_2913-912 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445216
|
TACACACA others(9): Show |
T | 105 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(102): Show | 105 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2913-9137_2913-912 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445216 | ||||||
| chr13:44445250
|
CACAG | C | 5 | a0001c0005t0004g0240a0004c0004t0003g0223a0004c0004t0003g0226others(2): Show | 5 | HG00733.hp1 HG01981.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-9159_2913-915 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445250 | ||||||
| chr13:44445252
|
CAG | C | 3 | a0001c0005t0004g0238a0001c0006t0006g0003a0001c0006t0021g0232 | 3 | HG02647.hp1 HG03471.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2913-9159_2913-915 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445252 | ||||||
| chr13:44445254
|
G | C | 13 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(10): Show | 13 | HG00323.hp1 HG01928.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-9159C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445254 | ||||||
| chr13:44445328
|
C | CA | 91 | a0001c0001t0001g0020a0001c0001t0001g0160a0001c0001t0001g0168others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2913-9234dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445328 | ||||||
| chr13:44445600
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2913-9505T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445600 | ||||||
| chr13:44445681
|
A | G | 7 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-9586T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445681 | ||||||
| chr13:44445782
|
T | C | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-9687A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445782 | ||||||
| chr13:44445983
|
G | C | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-9888C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44445983 | ||||||
| chr13:44446309
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2913-10214T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446309 | ||||||
| chr13:44446424
|
G | A | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-10329C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446424 | ||||||
| chr13:44446555
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2913-10460G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446555 | ||||||
| chr13:44446681
|
T | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | NA18952.hp2 NA18966.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-10586A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446681 | ||||||
| chr13:44446760
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2913-10665T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446760 | ||||||
| chr13:44446766
|
A | G | 1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2913-10671T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446766 | ||||||
| chr13:44446769
|
G | A | 1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2913-10674C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446769 | ||||||
| chr13:44446769
|
G | GGAA | 190 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.2913-10677_2913-10 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446769 | ||||||
| chr13:44446778
|
G | A | 19 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2913-10683C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446778 | ||||||
| chr13:44446781
|
A | G | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-10686T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446781 | ||||||
| chr13:44446787
|
G | A | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-10692C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446787 | ||||||
| chr13:44446790
|
G | GGAGGAGG others(5): Show |
80 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2913-10707_2913-10 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446790 | ||||||
| chr13:44446790
|
G | GGAGGAGG others(17): Show |
1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2913-10696_2913-10 others(30): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446790 | ||||||
| chr13:44446794
|
GAGGAGGA others(2): Show |
G | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-10708_2913-10 others(15): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446794 | ||||||
| chr13:44446803
|
A | G | 190 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.2913-10708T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446803 | ||||||
| chr13:44446856
|
AAAG | A | 7 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-10764_2913-10 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446856 | ||||||
| chr13:44446875
|
C | CATA | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2913-10783_2913-10 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446875 | ||||||
| chr13:44446887
|
T | A | 212 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2913-10792A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446887 | ||||||
| chr13:44446995
|
G | T | 222 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2913-10900C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44446995 | ||||||
| chr13:44447100
|
A | G | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-11005T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447100 | ||||||
| chr13:44447126
|
G | A | 1 | a0001c0001t0014g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2913-11031C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447126 | ||||||
| chr13:44447146
|
C | CT | 8 | a0001c0001t0002g0144a0001c0001t0004g0235a0001c0001t0004g0236others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-11052dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447146 | ||||||
| chr13:44447259
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2913-11164A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447259 | ||||||
| chr13:44447744
|
A | T | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-11649T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447744 | ||||||
| chr13:44447826
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2913-11731C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447826 | ||||||
| chr13:44447833
|
C | CT | 154 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2913-11739dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447833 | ||||||
| chr13:44447833
|
C | CTT | 12 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0033others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2913-11740_2913-11 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447833 | ||||||
| chr13:44447833
|
CT | C | 7 | a0001c0001t0004g0235a0001c0001t0006g0047a0001c0005t0004g0238others(4): Show | 7 | HG00323.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-11739delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44447833 | ||||||
| chr13:44448044
|
T | C | 21 | a0001c0001t0003g0036a0001c0001t0004g0235a0001c0001t0004g0236others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2913-11949A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448044 | ||||||
| chr13:44448138
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2913-12043A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448138 | ||||||
| chr13:44448352
|
T | C | 3 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047 | 3 | HG02257.hp1 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2913-12257A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448352 | ||||||
| chr13:44448356
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2913-12261G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448356 | ||||||
| chr13:44448391
|
C | T | 6 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0006g0047others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-12296G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448391 | ||||||
| chr13:44448516
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2913-12421A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448516 | ||||||
| chr13:44448614
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2913-12519T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448614 | ||||||
| chr13:44448709
|
TTA | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-12616_2913-12 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448709 | ||||||
| chr13:44448866
|
G | A | 3 | a0001c0001t0002g0112a0001c0001t0002g0155a0001c0010t0002g0214 | 3 | HG01074.hp1 HG02602.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2913-12771C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448866 | ||||||
| chr13:44448892
|
C | CGT | 89 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(86): Show | 89 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2913-12799_2913-12 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448892 | ||||||
| chr13:44448892
|
C | CGTGT | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-12801_2913-12 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448892 | ||||||
| chr13:44448892
|
C | CGTGTGT | 3 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0008g0234 | 3 | HG02280.hp1 HG03098.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2913-12803_2913-12 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448892 | ||||||
| chr13:44448892
|
CGT | C | 28 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0050others(25): Show | 28 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.2913-12799_2913-12 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448892 | ||||||
| chr13:44448928
|
C | G | 24 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0002g0037others(21): Show | 24 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.2913-12833G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448928 | ||||||
| chr13:44448950
|
A | G | 4 | a0004c0004t0003g0223a0004c0004t0003g0226a0004c0004t0007g0227others(1): Show | 4 | HG00733.hp1 HG01981.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-12855T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448950 | ||||||
| chr13:44448968
|
G | C | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2913-12873C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448968 | ||||||
| chr13:44448970
|
T | C | 1 | a0001c0001t0018g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2913-12875A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44448970 | ||||||
| chr13:44449222
|
G | T | 20 | a0001c0001t0001g0062a0001c0001t0001g0203a0001c0001t0003g0036others(17): Show | 20 | HG00323.hp1 HG00733.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2913-13127C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449222 | ||||||
| chr13:44449244
|
C | T | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-13149G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449244 | ||||||
| chr13:44449309
|
C | T | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-13214G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449309 | ||||||
| chr13:44449320
|
A | T | 80 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2913-13225T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449320 | ||||||
| chr13:44449480
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-13385G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449480 | ||||||
| chr13:44449687
|
AAAT | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-13595_2913-13 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449687 | ||||||
| chr13:44449819
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2913-13724A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449819 | ||||||
| chr13:44449834
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2913-13739A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44449834 | ||||||
| chr13:44450126
|
CA | C | 9 | a0001c0001t0002g0015a0001c0001t0002g0112a0001c0001t0002g0127others(6): Show | 9 | HG00140.hp2 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2913-14032delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450126 | ||||||
| chr13:44450128
|
A | T | 9 | a0001c0001t0002g0015a0001c0001t0002g0112a0001c0001t0002g0127others(6): Show | 9 | HG00140.hp2 HG01070.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2913-14033T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450128 | ||||||
| chr13:44450135
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2913-14040C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450135 | ||||||
| chr13:44450234
|
T | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-14139A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450234 | ||||||
| chr13:44450294
|
A | AG | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-14200dupC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450294 | ||||||
| chr13:44450325
|
T | G | 24 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.2913-14230A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450325 | ||||||
| chr13:44450761
|
C | T | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-14666G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450761 | ||||||
| chr13:44450778
|
T | A | 20 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0003g0036others(17): Show | 20 | HG00323.hp1 HG00733.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2913-14683A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450778 | ||||||
| chr13:44450873
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2913-14778A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450873 | ||||||
| chr13:44450914
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2913-14819C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44450914 | ||||||
| chr13:44451565
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-15470T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44451565 | ||||||
| chr13:44451736
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-15641C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44451736 | ||||||
| chr13:44451807
|
C | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-15712G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44451807 | ||||||
| chr13:44451936
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-15841C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44451936 | ||||||
| chr13:44452084
|
G | T | 3 | a0001c0001t0002g0140a0001c0001t0005g0001a0001c0001t0005g0002 | 3 | HG00558.hp1 HG02015.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.2913-15989C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452084 | ||||||
| chr13:44452096
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00597.hp1 NA18954.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-16001C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452096 | ||||||
| chr13:44452446
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2913-16351C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452446 | ||||||
| chr13:44452457
|
C | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(5): Show | 8 | HG02080.hp1 HG02083.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-16362G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452457 | ||||||
| chr13:44452566
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0002g0143 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2913-16471C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452566 | ||||||
| chr13:44452593
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-16498A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452593 | ||||||
| chr13:44452752
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-16657G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44452752 | ||||||
| chr13:44453155
|
T | A | 1 | a0001c0001t0001g0179 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2913-17060A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453155 | ||||||
| chr13:44453293
|
A | ACTT | 212 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.2913-17201_2913-17 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453293 | ||||||
| chr13:44453321
|
A | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0209a0001c0001t0001g0210others(3): Show | 6 | NA18952.hp2 NA18966.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-17226T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453321 | ||||||
| chr13:44453364
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00597.hp1 NA18954.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-17269A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453364 | ||||||
| chr13:44453570
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0002g0037 | 3 | HG03041.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-17475C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453570 | ||||||
| chr13:44453697
|
G | C | 2 | a0001c0001t0001g0191a0001c0001t0016g0192 | 2 | HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2913-17602C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453697 | ||||||
| chr13:44453747
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2913-17652A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453747 | ||||||
| chr13:44453843
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2913-17748C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453843 | ||||||
| chr13:44453865
|
A | G | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-17770T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44453865 | ||||||
| chr13:44454018
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2913-17923G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454018 | ||||||
| chr13:44454052
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2913-17957C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454052 | ||||||
| chr13:44454239
|
G | A | 1 | a0001c0010t0002g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2913-18144C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454239 | ||||||
| chr13:44454391
|
A | G | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-18296T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454391 | ||||||
| chr13:44454426
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0060others(2): Show | 5 | HG00544.hp2 HG01255.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-18331G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454426 | ||||||
| chr13:44454562
|
T | TTTACTAT others(1): Show |
18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-18475_2913-18 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454562 | ||||||
| chr13:44454715
|
A | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-18620T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454715 | ||||||
| chr13:44454850
|
TATC | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.2913-18758_2913-18 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454850 | ||||||
| chr13:44454865
|
T | C | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2913-18770A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454865 | ||||||
| chr13:44454929
|
A | T | 6 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0005t0004g0238others(3): Show | 6 | HG01975.hp2 HG01978.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-18834T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44454929 | ||||||
| chr13:44455085
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2913-18990T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455085 | ||||||
| chr13:44455187
|
T | C | 128 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(125): Show | 128 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.2913-19092A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455187 | ||||||
| chr13:44455242
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2913-19147C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455242 | ||||||
| chr13:44455269
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2913-19174G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455269 | ||||||
| chr13:44455377
|
A | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19282T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455377 | ||||||
| chr13:44455429
|
A | G | 128 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(125): Show | 128 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.2913-19334T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455429 | ||||||
| chr13:44455529
|
C | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0079others(3): Show | 6 | HG01070.hp2 HG01074.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-19434G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455529 | ||||||
| chr13:44455597
|
A | G | 78 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.2913-19502T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455597 | ||||||
| chr13:44455729
|
C | T | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19634G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455729 | ||||||
| chr13:44455774
|
C | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0141 | 2 | NA19002.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2913-19679G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455774 | ||||||
| chr13:44455815
|
A | G | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19720T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455815 | ||||||
| chr13:44455943
|
A | AAG | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19850_2913-19 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455943 | ||||||
| chr13:44455973
|
A | G | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19878T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44455973 | ||||||
| chr13:44456000
|
G | A | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-19905C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456000 | ||||||
| chr13:44456043
|
T | C | 110 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(107): Show | 110 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2913-19948A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456043 | ||||||
| chr13:44456063
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-19968A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456063 | ||||||
| chr13:44456086
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | HG00673.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2913-19991G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456086 | ||||||
| chr13:44456135
|
G | A | 1 | a0003c0003t0003g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2913-20040C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456135 | ||||||
| chr13:44456168
|
G | A | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-20073C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456168 | ||||||
| chr13:44456200
|
T | C | 110 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(107): Show | 110 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2913-20105A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456200 | ||||||
| chr13:44456238
|
A | G | 128 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(125): Show | 128 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.2913-20143T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456238 | ||||||
| chr13:44456398
|
G | C | 1 | a0001c0001t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2913-20303C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456398 | ||||||
| chr13:44456562
|
G | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-20467C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456562 | ||||||
| chr13:44456663
|
C | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.2913-20568G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44456663 | ||||||
| chr13:44457241
|
C | T | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-21146G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457241 | ||||||
| chr13:44457250
|
G | A | 2 | a0001c0001t0001g0170a0001c0005t0009g0237 | 2 | HG00639.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2913-21155C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457250 | ||||||
| chr13:44457308
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2913-21213A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457308 | ||||||
| chr13:44457358
|
A | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-21263T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457358 | ||||||
| chr13:44457517
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-21422C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457517 | ||||||
| chr13:44457637
|
C | CA | 76 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(73): Show | 76 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2913-21543dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457637 | ||||||
| chr13:44457637
|
C | CAA | 12 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0106others(9): Show | 12 | HG02056.hp2 HG02572.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2913-21544_2913-21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457637 | ||||||
| chr13:44457637
|
C | CAAA | 36 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(33): Show | 36 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.2913-21545_2913-21 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457637 | ||||||
| chr13:44457637
|
CA | C | 82 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.2913-21543delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457637 | ||||||
| chr13:44457647
|
A | T | 1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2913-21552T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457647 | ||||||
| chr13:44457927
|
C | A | 2 | a0001c0006t0006g0003a0001c0006t0021g0232 | 2 | HG02647.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2913-21832G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457927 | ||||||
| chr13:44457953
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2913-21858T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44457953 | ||||||
| chr13:44458607
|
C | G | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-22512G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44458607 | ||||||
| chr13:44458815
|
A | G | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-22720T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44458815 | ||||||
| chr13:44458925
|
A | T | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-22830T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44458925 | ||||||
| chr13:44459030
|
T | A | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-22935A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459030 | ||||||
| chr13:44459030
|
T | G | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-22935A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459030 | ||||||
| chr13:44459059
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2913-22964C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459059 | ||||||
| chr13:44459101
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2913-23006G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459101 | ||||||
| chr13:44459370
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-23275A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459370 | ||||||
| chr13:44459521
|
C | T | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-23426G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459521 | ||||||
| chr13:44459776
|
C | T | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-23681G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459776 | ||||||
| chr13:44459798
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2913-23703C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459798 | ||||||
| chr13:44459910
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-23815A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44459910 | ||||||
| chr13:44460111
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2913-24016T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460111 | ||||||
| chr13:44460328
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-24233C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460328 | ||||||
| chr13:44460441
|
A | T | 1 | a0001c0001t0002g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2913-24346T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460441 | ||||||
| chr13:44460508
|
A | AT | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-24414dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460508 | ||||||
| chr13:44460589
|
C | A | 1 | a0001c0001t0002g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2913-24494G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460589 | ||||||
| chr13:44460669
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2913-24574C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460669 | ||||||
| chr13:44460678
|
G | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-24583C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44460678 | ||||||
| chr13:44461192
|
G | T | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-25097C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461192 | ||||||
| chr13:44461237
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2913-25142A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461237 | ||||||
| chr13:44461259
|
C | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-25164G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461259 | ||||||
| chr13:44461290
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2913-25195T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461290 | ||||||
| chr13:44461363
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2913-25268T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461363 | ||||||
| chr13:44461623
|
T | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-25528A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461623 | ||||||
| chr13:44461636
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2913-25541G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461636 | ||||||
| chr13:44461683
|
T | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-25588A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461683 | ||||||
| chr13:44461766
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2913-25671C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461766 | ||||||
| chr13:44461791
|
C | T | 4 | a0001c0001t0002g0116a0001c0001t0002g0119a0001c0001t0002g0129others(1): Show | 4 | HG02027.hp2 NA19002.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-25696G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461791 | ||||||
| chr13:44461884
|
G | A | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-25789C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44461884 | ||||||
| chr13:44462241
|
G | GA | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-26147dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44462241 | ||||||
| chr13:44462429
|
A | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2913-26334T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44462429 | ||||||
| chr13:44462644
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-26549C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44462644 | ||||||
| chr13:44463029
|
A | G | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-26934T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463029 | ||||||
| chr13:44463213
|
C | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-27118G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463213 | ||||||
| chr13:44463239
|
T | C | 2 | a0001c0001t0008g0233a0001c0001t0008g0234 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2913-27144A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463239 | ||||||
| chr13:44463771
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-27676C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463771 | ||||||
| chr13:44463969
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2913-27874G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463969 | ||||||
| chr13:44463994
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-27899C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44463994 | ||||||
| chr13:44464002
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2913-27907C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464002 | ||||||
| chr13:44464321
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2913-28226G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464321 | ||||||
| chr13:44464523
|
G | A | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-28428C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464523 | ||||||
| chr13:44464538
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2913-28443A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464538 | ||||||
| chr13:44464655
|
G | A | 2 | a0001c0001t0001g0205a0005c0007t0001g0012 | 2 | HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2913-28560C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464655 | ||||||
| chr13:44464778
|
C | A | 1 | a0001c0001t0001g0182 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2913-28683G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464778 | ||||||
| chr13:44464837
|
C | T | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-28742G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464837 | ||||||
| chr13:44464936
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2913-28841A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464936 | ||||||
| chr13:44464941
|
AT | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-28847delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464941 | ||||||
| chr13:44464982
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2913-28887G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44464982 | ||||||
| chr13:44465013
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2913-28918A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465013 | ||||||
| chr13:44465054
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-28959G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465054 | ||||||
| chr13:44465222
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02074.hp2 NA18947.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2913-29127C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465222 | ||||||
| chr13:44465305
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-29210C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465305 | ||||||
| chr13:44465377
|
G | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-29282C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465377 | ||||||
| chr13:44465400
|
A | G | 1 | a0001c0001t0010g0126 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2913-29305T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465400 | ||||||
| chr13:44465486
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-29391C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465486 | ||||||
| chr13:44465710
|
C | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.2913-29615G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465710 | ||||||
| chr13:44465711
|
G | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-29616C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465711 | ||||||
| chr13:44465921
|
T | C | 101 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(98): Show | 101 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2913-29826A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465921 | ||||||
| chr13:44465950
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2913-29855C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465950 | ||||||
| chr13:44465979
|
A | AAAAC | 223 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2913-29888_2913-29 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465979 | ||||||
| chr13:44465979
|
A | AAAACAAA others(1): Show |
13 | a0001c0001t0001g0159a0001c0001t0003g0036a0001c0014t0003g0229others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-29892_2913-29 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44465979 | ||||||
| chr13:44466040
|
T | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-29945A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466040 | ||||||
| chr13:44466079
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2913-29984T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466079 | ||||||
| chr13:44466496
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-30401A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466496 | ||||||
| chr13:44466566
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-30471A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466566 | ||||||
| chr13:44466762
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 56 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2913-30667G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466762 | ||||||
| chr13:44466775
|
G | GA | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-30681dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466775 | ||||||
| chr13:44466804
|
C | T | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-30709G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466804 | ||||||
| chr13:44466885
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2913-30790C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466885 | ||||||
| chr13:44466912
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2913-30817G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466912 | ||||||
| chr13:44466983
|
C | T | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-30888G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44466983 | ||||||
| chr13:44467086
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0002g0037 | 3 | HG03041.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-30991G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467086 | ||||||
| chr13:44467093
|
T | C | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-30998A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467093 | ||||||
| chr13:44467178
|
C | A | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-31083G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467178 | ||||||
| chr13:44467178
|
CA | C | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-31084delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467178 | ||||||
| chr13:44467179
|
A | AC | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-31085_2913-31 others(7): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467179 | ||||||
| chr13:44467327
|
A | G | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-31232T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467327 | ||||||
| chr13:44467401
|
G | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(6): Show | 9 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.2913-31306C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467401 | ||||||
| chr13:44467891
|
G | C | 67 | a0001c0001t0001g0121a0001c0001t0001g0182a0001c0001t0002g0015others(64): Show | 67 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2913-31796C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467891 | ||||||
| chr13:44467998
|
ACG | A | 18 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2913-31905_2913-31 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44467998 | ||||||
| chr13:44468001
|
C | T | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-31906G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468001 | ||||||
| chr13:44468002
|
G | A | 192 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.2913-31907C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468002 | ||||||
| chr13:44468059
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0069 | 2 | HG02074.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.2913-31964T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468059 | ||||||
| chr13:44468296
|
GTACACTA others(666): Show |
G | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-32874_2913-32 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468296 | ||||||
| chr13:44468654
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2913-32559C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468654 | ||||||
| chr13:44468679
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2913-32584C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468679 | ||||||
| chr13:44468954
|
ATTCT | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-32863_2913-32 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44468954 | ||||||
| chr13:44469079
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2913-32984C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469079 | ||||||
| chr13:44469135
|
C | G | 1 | a0001c0001t0013g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2913-33040G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469135 | ||||||
| chr13:44469303
|
G | A | 23 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(20): Show | 23 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2913-33208C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469303 | ||||||
| chr13:44469421
|
CTACTTCA others(78): Show |
C | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2913-33411_2913-33 others(91): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469421 | ||||||
| chr13:44469742
|
TTATC | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00597.hp2 NA18941.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-33651_2913-33 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469742 | ||||||
| chr13:44469748
|
A | G | 57 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(54): Show | 57 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2913-33653T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44469748 | ||||||
| chr13:44470360
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2913-34265G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44470360 | ||||||
| chr13:44471077
|
T | C | 220 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2913-34982A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471077 | ||||||
| chr13:44471104
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2913-35009T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471104 | ||||||
| chr13:44471118
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2913-35023G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471118 | ||||||
| chr13:44471411
|
C | T | 1 | a0001c0005t0009g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2913-35316G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471411 | ||||||
| chr13:44471518
|
A | G | 1 | a0002c0002t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2913-35423T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471518 | ||||||
| chr13:44471761
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2913-35666A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44471761 | ||||||
| chr13:44472296
|
T | C | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2913-36201A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44472296 | ||||||
| chr13:44472528
|
C | T | 1 | a0003c0003t0003g0221 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2913-36433G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44472528 | ||||||
| chr13:44472663
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2913-36568A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44472663 | ||||||
| chr13:44472817
|
A | G | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-36722T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44472817 | ||||||
| chr13:44472884
|
A | G | 2 | a0001c0001t0004g0235a0001c0001t0004g0236 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2913-36789T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44472884 | ||||||
| chr13:44473120
|
C | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG01891.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2913-37025G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473120 | ||||||
| chr13:44473264
|
G | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-37169C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473264 | ||||||
| chr13:44473465
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0153 | 3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2913-37370T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473465 | ||||||
| chr13:44473605
|
ATG | A | 236 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(233): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2913-37512_2913-37 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473605 | ||||||
| chr13:44473645
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2913-37550A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473645 | ||||||
| chr13:44473710
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2913-37615T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473710 | ||||||
| chr13:44473863
|
T | G | 26 | a0001c0001t0001g0106a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 26 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.2913-37768A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473863 | ||||||
| chr13:44473912
|
G | C | 1 | a0001c0014t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2913-37817C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44473912 | ||||||
| chr13:44474362
|
C | G | 14 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-38267G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44474362 | ||||||
| chr13:44474552
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2913-38457A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44474552 | ||||||
| chr13:44474696
|
A | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(83): Show | 86 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2913-38601T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44474696 | ||||||
| chr13:44474843
|
A | C | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-38748T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44474843 | ||||||
| chr13:44474866
|
C | G | 14 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2913-38771G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44474866 | ||||||
| chr13:44475111
|
G | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-39016C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475111 | ||||||
| chr13:44475362
|
T | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-39267A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475362 | ||||||
| chr13:44475465
|
C | CA | 18 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.2913-39371dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475465 | ||||||
| chr13:44475465
|
CA | C | 100 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(97): Show | 100 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2913-39371delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475465 | ||||||
| chr13:44475637
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2913-39542T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475637 | ||||||
| chr13:44475786
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2913-39691A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475786 | ||||||
| chr13:44475829
|
T | C | 14 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2913-39734A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44475829 | ||||||
| chr13:44476077
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-39982G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44476077 | ||||||
| chr13:44476252
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2913-40157A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44476252 | ||||||
| chr13:44476525
|
C | A | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-40430G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44476525 | ||||||
| chr13:44476606
|
G | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-40511C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44476606 | ||||||
| chr13:44477244
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-41149A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44477244 | ||||||
| chr13:44477369
|
T | C | 2 | a0001c0006t0006g0003a0001c0006t0021g0232 | 2 | HG02647.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2913-41274A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44477369 | ||||||
| chr13:44477638
|
A | AT | 80 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2913-41544dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44477638 | ||||||
| chr13:44477644
|
T | C | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-41549A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44477644 | ||||||
| chr13:44478024
|
A | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-41929T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478024 | ||||||
| chr13:44478129
|
G | C | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-42034C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478129 | ||||||
| chr13:44478539
|
G | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-42444C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478539 | ||||||
| chr13:44478549
|
T | TG | 15 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-42455dupC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478549 | ||||||
| chr13:44478894
|
A | AGT | 14 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0182others(11): Show | 14 | HG00735.hp1 HG01928.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-42801_2913-42 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478894 | ||||||
| chr13:44478894
|
A | AGTGT | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2913-42803_2913-42 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44478894 | ||||||
| chr13:44479015
|
T | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-42920A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479015 | ||||||
| chr13:44479117
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01496.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2913-43022G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479117 | ||||||
| chr13:44479248
|
G | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-43153C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479248 | ||||||
| chr13:44479270
|
G | A | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-43175C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479270 | ||||||
| chr13:44479275
|
C | T | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-43180G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479275 | ||||||
| chr13:44479322
|
A | AT | 105 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(102): Show | 105 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2913-43228dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479322 | ||||||
| chr13:44479322
|
AT | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0186a0001c0001t0004g0236others(2): Show | 5 | HG01243.hp1 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-43228delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479322 | ||||||
| chr13:44479381
|
C | T | 109 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(106): Show | 109 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2913-43286G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479381 | ||||||
| chr13:44479406
|
C | T | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-43311G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479406 | ||||||
| chr13:44479429
|
T | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00597.hp2 NA18941.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-43334A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479429 | ||||||
| chr13:44479442
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2913-43347G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479442 | ||||||
| chr13:44479811
|
C | T | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-43716G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44479811 | ||||||
| chr13:44480089
|
T | TAAG | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-43997_2913-43 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480089 | ||||||
| chr13:44480097
|
G | T | 1 | a0009c0008t0001g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2913-44002C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480097 | ||||||
| chr13:44480282
|
T | G | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-44187A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480282 | ||||||
| chr13:44480765
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2913-44670A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480765 | ||||||
| chr13:44480935
|
A | G | 1 | a0001c0001t0012g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2913-44840T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480935 | ||||||
| chr13:44480955
|
T | C | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-44860A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44480955 | ||||||
| chr13:44481780
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-45685G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44481780 | ||||||
| chr13:44482017
|
C | G | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-45922G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482017 | ||||||
| chr13:44482264
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2913-46169C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482264 | ||||||
| chr13:44482332
|
C | T | 15 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-46237G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482332 | ||||||
| chr13:44482488
|
G | C | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2913-46393C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482488 | ||||||
| chr13:44482495
|
C | T | 4 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0009others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-46400G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482495 | ||||||
| chr13:44482607
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0002g0183 | 2 | HG01243.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2913-46512G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44482607 | ||||||
| chr13:44483054
|
A | G | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-46959T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483054 | ||||||
| chr13:44483212
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2913-47117C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483212 | ||||||
| chr13:44483216
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG00558.hp2 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-47121C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483216 | ||||||
| chr13:44483335
|
G | GA | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-47241dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483335 | ||||||
| chr13:44483409
|
C | A | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-47314G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483409 | ||||||
| chr13:44483454
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2913-47359C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483454 | ||||||
| chr13:44483477
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2913-47382G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483477 | ||||||
| chr13:44483685
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47590C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483685 | ||||||
| chr13:44483688
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47593A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483688 | ||||||
| chr13:44483689
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47594A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483689 | ||||||
| chr13:44483691
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47596A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483691 | ||||||
| chr13:44483692
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47597C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483692 | ||||||
| chr13:44483696
|
C | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47601G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483696 | ||||||
| chr13:44483699
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47604C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483699 | ||||||
| chr13:44483701
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47606A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483701 | ||||||
| chr13:44483702
|
C | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47607G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483702 | ||||||
| chr13:44483703
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47608A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483703 | ||||||
| chr13:44483705
|
C | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-47610G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483705 | ||||||
| chr13:44483710
|
ATTGGCTG others(581): Show |
A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-48203_2913-47 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483710 | ||||||
| chr13:44483720
|
C | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-47625G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44483720 | ||||||
| chr13:44484058
|
C | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0082 | 3 | HG00544.hp2 NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2913-47963G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484058 | ||||||
| chr13:44484230
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG01891.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2913-48135C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484230 | ||||||
| chr13:44484300
|
C | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-48205G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484300 | ||||||
| chr13:44484302
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-48207C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484302 | ||||||
| chr13:44484303
|
T | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-48208A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484303 | ||||||
| chr13:44484306
|
C | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2913-48211G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484306 | ||||||
| chr13:44484396
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2913-48301G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484396 | ||||||
| chr13:44484869
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2913-48774C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484869 | ||||||
| chr13:44484928
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0178 | 2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2913-48833T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44484928 | ||||||
| chr13:44485166
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-49071C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485166 | ||||||
| chr13:44485313
|
C | A | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-49218G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485313 | ||||||
| chr13:44485731
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2913-49636T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485731 | ||||||
| chr13:44485762
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2913-49667A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485762 | ||||||
| chr13:44485905
|
G | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-49810C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485905 | ||||||
| chr13:44485905
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-49810C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44485905 | ||||||
| chr13:44486168
|
T | C | 15 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-50073A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486168 | ||||||
| chr13:44486318
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2913-50223C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486318 | ||||||
| chr13:44486348
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2913-50253G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486348 | ||||||
| chr13:44486658
|
C | T | 1 | a0001c0001t0015g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2913-50563G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486658 | ||||||
| chr13:44486809
|
C | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-50714G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486809 | ||||||
| chr13:44486955
|
T | C | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-50860A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44486955 | ||||||
| chr13:44487028
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2913-50933T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487028 | ||||||
| chr13:44487314
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 56 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2913-51219G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487314 | ||||||
| chr13:44487325
|
C | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2913-51230G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487325 | ||||||
| chr13:44487355
|
T | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2913-51260A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487355 | ||||||
| chr13:44487407
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2913-51312C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487407 | ||||||
| chr13:44487454
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2913-51359C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487454 | ||||||
| chr13:44487498
|
C | CA | 20 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0046others(17): Show | 20 | HG01496.hp1 HG02056.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2913-51404dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487498 | ||||||
| chr13:44487498
|
C | CAA | 6 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0042others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-51405_2913-51 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487498 | ||||||
| chr13:44487498
|
CA | C | 141 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.2913-51404delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487498 | ||||||
| chr13:44487498
|
CAA | C | 25 | a0001c0001t0001g0061a0001c0001t0001g0154a0001c0001t0001g0186others(22): Show | 25 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.2913-51405_2913-51 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487498 | ||||||
| chr13:44487498
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2913-51418_2913-51 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487498 | ||||||
| chr13:44487521
|
A | G | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-51426T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487521 | ||||||
| chr13:44487523
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2913-51428T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487523 | ||||||
| chr13:44487703
|
T | TA | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-51609dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44487703 | ||||||
| chr13:44488048
|
A | C | 116 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(113): Show | 116 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.2913-51953T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488048 | ||||||
| chr13:44488051
|
C | CT | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-51957dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488051 | ||||||
| chr13:44488135
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2913-52040A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488135 | ||||||
| chr13:44488213
|
G | A | 1 | a0007c0009t0002g0014 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2913-52118C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488213 | ||||||
| chr13:44488340
|
C | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-52245G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488340 | ||||||
| chr13:44488468
|
C | G | 1 | a0009c0008t0001g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2913-52373G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488468 | ||||||
| chr13:44488487
|
G | A | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-52392C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488487 | ||||||
| chr13:44488982
|
AAAG | A | 3 | a0001c0001t0002g0102a0001c0001t0002g0148a0001c0010t0002g0214 | 3 | HG01943.hp1 HG02602.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2913-52890_2913-52 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488982 | ||||||
| chr13:44488999
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2913-52904T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44488999 | ||||||
| chr13:44489206
|
C | CA | 89 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 89 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.2913-53112dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489206 | ||||||
| chr13:44489206
|
C | CAA | 7 | a0001c0001t0001g0121a0001c0001t0004g0235a0001c0001t0004g0236others(4): Show | 7 | HG00597.hp1 HG02257.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2913-53113_2913-53 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489206 | ||||||
| chr13:44489206
|
CA | C | 77 | a0001c0001t0001g0106a0001c0001t0001g0160a0001c0001t0001g0166others(74): Show | 77 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2913-53112delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489206 | ||||||
| chr13:44489418
|
A | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-53323T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489418 | ||||||
| chr13:44489666
|
G | T | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-53571C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489666 | ||||||
| chr13:44489720
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2913-53625C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489720 | ||||||
| chr13:44489911
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2913-53816C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44489911 | ||||||
| chr13:44490043
|
A | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-53948T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490043 | ||||||
| chr13:44490329
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0060 | 2 | NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2913-54234T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490329 | ||||||
| chr13:44490387
|
G | C | 3 | a0001c0001t0002g0112a0001c0001t0002g0117a0001c0001t0002g0155 | 3 | HG01074.hp1 HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2913-54292C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490387 | ||||||
| chr13:44490594
|
T | C | 103 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2913-54499A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490594 | ||||||
| chr13:44490663
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2913-54568G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490663 | ||||||
| chr13:44490689
|
G | A | 3 | a0001c0001t0002g0112a0001c0001t0002g0117a0001c0001t0002g0155 | 3 | HG01074.hp1 HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2913-54594C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490689 | ||||||
| chr13:44490935
|
A | AAT | 67 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0166others(64): Show | 67 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2913-54841_2913-54 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490935 | ||||||
| chr13:44490937
|
A | T | 118 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(115): Show | 118 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2913-54842T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44490937 | ||||||
| chr13:44491145
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2913-55050G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491145 | ||||||
| chr13:44491211
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0090a0001c0001t0011g0039others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-55116C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491211 | ||||||
| chr13:44491221
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0119a0001c0001t0002g0141 | 3 | NA19002.hp1 NA19063.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2913-55126T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491221 | ||||||
| chr13:44491248
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0096 | 3 | HG02074.hp1 HG02132.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2913-55153C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491248 | ||||||
| chr13:44491255
|
G | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-55160C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491255 | ||||||
| chr13:44491275
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2913-55180G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491275 | ||||||
| chr13:44491276
|
G | A | 2 | a0004c0004t0003g0224a0008c0013t0003g0222 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2913-55181C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491276 | ||||||
| chr13:44491413
|
A | G | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-55318T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491413 | ||||||
| chr13:44491511
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00597.hp2 NA18941.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-55416C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491511 | ||||||
| chr13:44491570
|
G | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-55475C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491570 | ||||||
| chr13:44491756
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2913-55661A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491756 | ||||||
| chr13:44491875
|
G | A | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-55780C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491875 | ||||||
| chr13:44491977
|
T | G | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-55882A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44491977 | ||||||
| chr13:44492162
|
T | TAAAAATA others(335): Show |
1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2913-56068_2913-56 others(348): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44492162 | ||||||
| chr13:44492162
|
T | TAAAAATA others(337): Show |
1 | a0001c0001t0018g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2913-56068_2913-56 others(350): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44492162 | ||||||
| chr13:44492174
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2913-56079G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44492174 | ||||||
| chr13:44492625
|
C | T | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-56530G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44492625 | ||||||
| chr13:44493167
|
C | A | 219 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2913-57072G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44493167 | ||||||
| chr13:44493230
|
T | C | 1 | a0003c0003t0003g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2913-57135A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44493230 | ||||||
| chr13:44493398
|
G | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-57303C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44493398 | ||||||
| chr13:44493650
|
C | T | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-57555G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44493650 | ||||||
| chr13:44493766
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2913-57671A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44493766 | ||||||
| chr13:44494126
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2913-58031T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494126 | ||||||
| chr13:44494325
|
G | A | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.2913-58230C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494325 | ||||||
| chr13:44494375
|
C | CA | 12 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 12 | HG01975.hp2 HG02615.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2913-58281dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAA | 46 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0044others(43): Show | 46 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2913-58282_2913-58 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAAA | 21 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0170others(18): Show | 21 | HG00597.hp1 HG00639.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.2913-58283_2913-58 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAAAA | 15 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0001g0169others(12): Show | 15 | HG00544.hp1 HG01975.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-58284_2913-58 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAAAAA | 12 | a0001c0001t0001g0050a0001c0001t0001g0161a0001c0001t0001g0162others(9): Show | 12 | HG01516.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2913-58285_2913-58 others(11): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAAAAAA | 5 | a0001c0001t0001g0032a0001c0001t0001g0160a0001c0001t0001g0171others(2): Show | 5 | HG03471.hp1 HG04199.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-58286_2913-58 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
C | CAAAAAAA others(3): Show |
1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-58290_2913-58 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
CA | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0076others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.2913-58281delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
CAA | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(73): Show | 76 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2913-58282_2913-58 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2913-58290_2913-58 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494375
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0006g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2913-58293_2913-58 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494375 | ||||||
| chr13:44494500
|
C | G | 219 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2913-58405G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494500 | ||||||
| chr13:44494522
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0090a0001c0001t0011g0039others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-58427G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494522 | ||||||
| chr13:44494602
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2913-58507G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494602 | ||||||
| chr13:44494615
|
A | C | 1 | a0002c0002t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2913-58520T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494615 | ||||||
| chr13:44494666
|
T | C | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2913-58571A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494666 | ||||||
| chr13:44494914
|
A | C | 6 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0128others(3): Show | 6 | HG00735.hp2 HG01099.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-58819T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44494914 | ||||||
| chr13:44495295
|
GA | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0159others(7): Show | 10 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.2913-59201delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495295 | ||||||
| chr13:44495295
|
GAA | G | 13 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2913-59202_2913-59 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495295 | ||||||
| chr13:44495295
|
GAAA | G | 6 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(3): Show | 6 | HG02148.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-59203_2913-59 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495295 | ||||||
| chr13:44495309
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2913-59214T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495309 | ||||||
| chr13:44495330
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01496.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2913-59235T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495330 | ||||||
| chr13:44495991
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2913-59896G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44495991 | ||||||
| chr13:44496004
|
C | A | 4 | a0004c0004t0003g0223a0004c0004t0003g0226a0004c0004t0007g0227others(1): Show | 4 | HG00733.hp1 HG01981.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2913-59909G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496004 | ||||||
| chr13:44496222
|
T | C | 68 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0121others(65): Show | 68 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2913-60127A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496222 | ||||||
| chr13:44496383
|
T | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-60288A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496383 | ||||||
| chr13:44496555
|
A | G | 117 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(114): Show | 117 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2913-60460T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496555 | ||||||
| chr13:44496685
|
CA | C | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-60591delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496685 | ||||||
| chr13:44496818
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2913-60723C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496818 | ||||||
| chr13:44496944
|
G | A | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.2913-60849C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44496944 | ||||||
| chr13:44497266
|
G | A | 6 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG02080.hp1 HG02083.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2913-61171C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44497266 | ||||||
| chr13:44497477
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2913-61382C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44497477 | ||||||
| chr13:44497566
|
G | GAAC | 2 | a0001c0006t0006g0003a0001c0006t0021g0232 | 2 | HG02647.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2913-61474_2913-61 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44497566 | ||||||
| chr13:44497635
|
T | G | 2 | a0001c0001t0001g0184a0001c0001t0002g0183 | 2 | HG01243.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2913-61540A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44497635 | ||||||
| chr13:44498088
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2913-61993G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498088 | ||||||
| chr13:44498098
|
A | C | 1 | a0001c0001t0002g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2913-62003T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498098 | ||||||
| chr13:44498099
|
C | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-62004G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498099 | ||||||
| chr13:44498100
|
C | CA | 15 | a0001c0001t0002g0067a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-62006dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498100 | ||||||
| chr13:44498229
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-62134A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498229 | ||||||
| chr13:44498299
|
A | AAAAC | 85 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0041others(82): Show | 85 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2913-62208_2913-62 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498299 | ||||||
| chr13:44498299
|
AAAAC | A | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-62208_2913-62 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498299 | ||||||
| chr13:44498385
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | HG00673.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2913-62290T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498385 | ||||||
| chr13:44498538
|
G | A | 2 | a0004c0004t0003g0224a0008c0013t0003g0222 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2913-62443C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498538 | ||||||
| chr13:44498720
|
C | T | 219 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2913-62625G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498720 | ||||||
| chr13:44498812
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2913-62717A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498812 | ||||||
| chr13:44498929
|
T | C | 2 | a0001c0005t0009g0237a0001c0005t0009g0239 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2913-62834A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44498929 | ||||||
| chr13:44499200
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2913-63105A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44499200 | ||||||
| chr13:44499400
|
T | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-63305A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44499400 | ||||||
| chr13:44499614
|
G | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.2913-63519C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44499614 | ||||||
| chr13:44499793
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2913-63698T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44499793 | ||||||
| chr13:44500076
|
G | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-63981C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500076 | ||||||
| chr13:44500237
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2913-64142A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500237 | ||||||
| chr13:44500308
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0016g0192 | 3 | HG02080.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2913-64213A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500308 | ||||||
| chr13:44500414
|
T | C | 2 | a0001c0001t0002g0123a0001c0001t0002g0125 | 2 | NA18947.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2913-64319A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500414 | ||||||
| chr13:44500692
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2913-64597C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500692 | ||||||
| chr13:44500732
|
T | C | 15 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-64637A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500732 | ||||||
| chr13:44500738
|
G | T | 1 | a0001c0001t0019g0138 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2913-64643C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500738 | ||||||
| chr13:44500745
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2913-64650G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44500745 | ||||||
| chr13:44501121
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2913-65026T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501121 | ||||||
| chr13:44501453
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2913-65358G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501453 | ||||||
| chr13:44501548
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2913-65453G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501548 | ||||||
| chr13:44501561
|
C | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG02572.hp2 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-65466G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501561 | ||||||
| chr13:44501562
|
C | CCCAGAGG others(3): Show |
14 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG02572.hp2 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2913-65468_2913-65 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501562 | ||||||
| chr13:44501579
|
G | A | 103 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(100): Show | 103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2913-65484C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44501579 | ||||||
| chr13:44502003
|
C | T | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-65908G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502003 | ||||||
| chr13:44502042
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-65947T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502042 | ||||||
| chr13:44502053
|
A | T | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-65958T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502053 | ||||||
| chr13:44502086
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2913-65991C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502086 | ||||||
| chr13:44502456
|
A | G | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-66361T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502456 | ||||||
| chr13:44502574
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2913-66479T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502574 | ||||||
| chr13:44502585
|
A | G | 1 | a0003c0003t0003g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2913-66490T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502585 | ||||||
| chr13:44502637
|
G | A | 19 | a0001c0001t0003g0036a0001c0005t0004g0238a0001c0005t0004g0240others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2913-66542C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502637 | ||||||
| chr13:44502654
|
G | A | 218 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.2913-66559C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502654 | ||||||
| chr13:44502661
|
TTTGACAG others(12): Show |
T | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2913-66585_2913-66 others(25): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502661 | ||||||
| chr13:44502714
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2913-66619G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502714 | ||||||
| chr13:44502718
|
G | A | 66 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0182others(63): Show | 66 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2913-66623C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502718 | ||||||
| chr13:44502855
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2913-66760G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44502855 | ||||||
| chr13:44503018
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2913-66923C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503018 | ||||||
| chr13:44503129
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2913-67034C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503129 | ||||||
| chr13:44503329
|
G | GA | 15 | a0001c0001t0003g0036a0001c0014t0003g0229a0003c0003t0003g0216others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2913-67235dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503329 | ||||||
| chr13:44503353
|
C | T | 115 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0032others(112): Show | 115 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.2913-67258G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503353 | ||||||
| chr13:44503369
|
G | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0095 | 3 | HG01167.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2913-67274C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503369 | ||||||
| chr13:44503434
|
G | C | 1 | a0001c0001t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2913-67339C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503434 | ||||||
| chr13:44503606
|
G | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.2913-67511C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503606 | ||||||
| chr13:44503612
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2913-67517T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503612 | ||||||
| chr13:44503719
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2913-67624A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503719 | ||||||
| chr13:44503834
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00597.hp1 NA18954.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-67739A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503834 | ||||||
| chr13:44503939
|
C | G | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2913-67844G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503939 | ||||||
| chr13:44503970
|
T | G | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2913-67875A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44503970 | ||||||
| chr13:44504127
|
A | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(96): Show | 99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2913-68032T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504127 | ||||||
| chr13:44504137
|
G | GA | 8 | a0001c0001t0001g0160a0001c0001t0001g0173a0001c0001t0001g0212others(5): Show | 8 | HG00733.hp2 HG01192.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-68043dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504137 | ||||||
| chr13:44504160
|
G | T | 98 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2913-68065C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504160 | ||||||
| chr13:44504241
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2913-68146T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504241 | ||||||
| chr13:44504393
|
C | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2913-68298G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504393 | ||||||
| chr13:44504550
|
G | T | 97 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2913-68455C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504550 | ||||||
| chr13:44504601
|
C | CA | 10 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0176others(7): Show | 10 | HG01070.hp1 HG01978.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.2913-68507dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504601 | ||||||
| chr13:44504601
|
CAA | C | 95 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2913-68508_2913-68 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504601 | ||||||
| chr13:44504601
|
CAAA | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG00323.hp2 HG01243.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2913-68509_2913-68 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504601 | ||||||
| chr13:44504623
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2913-68528T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504623 | ||||||
| chr13:44504945
|
A | T | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2912+68218T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44504945 | ||||||
| chr13:44505851
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2912+67312T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44505851 | ||||||
| chr13:44505923
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2912+67240A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44505923 | ||||||
| chr13:44506377
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2912+66786G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44506377 | ||||||
| chr13:44506380
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | HG00673.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2912+66783C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44506380 | ||||||
| chr13:44506429
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+66734G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44506429 | ||||||
| chr13:44506470
|
T | G | 1 | a0001c0001t0001g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2912+66693A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44506470 | ||||||
| chr13:44506948
|
C | A | 1 | a0008c0013t0003g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2912+66215G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44506948 | ||||||
| chr13:44507178
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2912+65985C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507178 | ||||||
| chr13:44507469
|
CT | C | 9 | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0060others(6): Show | 9 | HG00544.hp2 HG01255.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+65693delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507469 | ||||||
| chr13:44507628
|
A | T | 1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2912+65535T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507628 | ||||||
| chr13:44507802
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2912+65361G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507802 | ||||||
| chr13:44507900
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2912+65263A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507900 | ||||||
| chr13:44507954
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2912+65209A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44507954 | ||||||
| chr13:44508466
|
T | A | 26 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(23): Show | 26 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.2912+64697A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44508466 | ||||||
| chr13:44508787
|
G | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+64376C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44508787 | ||||||
| chr13:44508880
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2912+64283C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44508880 | ||||||
| chr13:44509255
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2912+63908T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509255 | ||||||
| chr13:44509386
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+63777G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509386 | ||||||
| chr13:44509508
|
C | T | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2912+63655G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509508 | ||||||
| chr13:44509528
|
T | TACTCAGG others(25): Show |
1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2912+63603_2912+63 others(38): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509528 | ||||||
| chr13:44509572
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2912+63591C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509572 | ||||||
| chr13:44509641
|
T | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(96): Show | 99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2912+63522A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509641 | ||||||
| chr13:44509950
|
C | CA | 13 | a0001c0001t0001g0020a0001c0001t0001g0158a0001c0001t0001g0165others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.2912+63212dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509950 | ||||||
| chr13:44509950
|
CA | C | 97 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0030others(94): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.2912+63212delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509950 | ||||||
| chr13:44509950
|
CAA | C | 5 | a0001c0001t0002g0127a0001c0001t0003g0036a0001c0006t0006g0003others(2): Show | 5 | HG00140.hp2 HG01167.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2912+63211_2912+63 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509950 | ||||||
| chr13:44509973
|
C | G | 1 | a0009c0008t0001g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2912+63190G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44509973 | ||||||
| chr13:44510000
|
G | A | 1 | a0004c0004t0003g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2912+63163C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510000 | ||||||
| chr13:44510092
|
G | C | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2912+63071C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510092 | ||||||
| chr13:44510103
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2912+63060C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510103 | ||||||
| chr13:44510219
|
T | TA | 7 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0081others(4): Show | 7 | HG02293.hp2 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+62943dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510219 | ||||||
| chr13:44510236
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2912+62927A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510236 | ||||||
| chr13:44510324
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2912+62839C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510324 | ||||||
| chr13:44510332
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+62831G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510332 | ||||||
| chr13:44510713
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+62450G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510713 | ||||||
| chr13:44510760
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2912+62403A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44510760 | ||||||
| chr13:44511086
|
T | G | 97 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2912+62077A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511086 | ||||||
| chr13:44511149
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2912+62014C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511149 | ||||||
| chr13:44511356
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2912+61807T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511356 | ||||||
| chr13:44511411
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2912+61752A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511411 | ||||||
| chr13:44511564
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | NA18952.hp2 NA18966.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+61599A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511564 | ||||||
| chr13:44511619
|
T | TAC | 57 | a0001c0001t0001g0020a0001c0001t0001g0081a0001c0001t0001g0106others(54): Show | 57 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2912+61542_2912+61 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511619 | ||||||
| chr13:44511619
|
T | TACAC | 32 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0061others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.2912+61540_2912+61 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511619 | ||||||
| chr13:44511619
|
TAC | T | 63 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(60): Show | 63 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2912+61542_2912+61 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511619 | ||||||
| chr13:44511805
|
AG | A | 26 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(23): Show | 26 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.2912+61357delC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44511805 | ||||||
| chr13:44512153
|
TTTTG | T | 5 | a0001c0001t0001g0090a0001c0001t0011g0039a0001c0001t0018g0084others(2): Show | 5 | HG01192.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+61006_2912+61 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512153 | ||||||
| chr13:44512230
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2912+60933G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512230 | ||||||
| chr13:44512448
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2912+60715A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512448 | ||||||
| chr13:44512640
|
T | G | 98 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2912+60523A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512640 | ||||||
| chr13:44512657
|
C | CTCTT | 98 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2912+60505_2912+60 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512657 | ||||||
| chr13:44512939
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2912+60224G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512939 | ||||||
| chr13:44512956
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+60207G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44512956 | ||||||
| chr13:44513063
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2912+60100A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513063 | ||||||
| chr13:44513158
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01496.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2912+60005G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513158 | ||||||
| chr13:44513234
|
G | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+59929C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513234 | ||||||
| chr13:44513352
|
T | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+59811A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513352 | ||||||
| chr13:44513381
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2912+59782C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513381 | ||||||
| chr13:44513823
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+59340C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513823 | ||||||
| chr13:44513955
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2912+59208G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44513955 | ||||||
| chr13:44514163
|
T | C | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+59000A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514163 | ||||||
| chr13:44514227
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2912+58936A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514227 | ||||||
| chr13:44514299
|
G | A | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.2912+58864C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514299 | ||||||
| chr13:44514390
|
G | GC | 14 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+58772dupG | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514390 | ||||||
| chr13:44514401
|
C | T | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+58762G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514401 | ||||||
| chr13:44514413
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG01891.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2912+58750T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514413 | ||||||
| chr13:44514571
|
A | C | 1 | a0001c0015t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2912+58592T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514571 | ||||||
| chr13:44514633
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02056.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2912+58530C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514633 | ||||||
| chr13:44514638
|
A | T | 98 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2912+58525T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514638 | ||||||
| chr13:44514791
|
C | T | 8 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2912+58372G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514791 | ||||||
| chr13:44514866
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2912+58297T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514866 | ||||||
| chr13:44514870
|
A | G | 71 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(68): Show | 71 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2912+58293T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44514870 | ||||||
| chr13:44515024
|
A | G | 2 | a0004c0004t0003g0224a0008c0013t0003g0222 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2912+58139T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515024 | ||||||
| chr13:44515314
|
T | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+57849A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515314 | ||||||
| chr13:44515315
|
A | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+57848T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515315 | ||||||
| chr13:44515362
|
G | A | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+57801C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515362 | ||||||
| chr13:44515400
|
A | G | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+57763T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515400 | ||||||
| chr13:44515402
|
A | G | 102 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2912+57761T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515402 | ||||||
| chr13:44515599
|
G | A | 183 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2912+57564C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515599 | ||||||
| chr13:44515602
|
TAATTTTG others(9557): Show |
T | 1 | a0001c0001t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2912+47997_2912+57 others(6): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515602 | ||||||
| chr13:44515630
|
G | A | 77 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2912+57533C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515630 | ||||||
| chr13:44515685
|
C | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+57478G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515685 | ||||||
| chr13:44515715
|
G | C | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2912+57448C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515715 | ||||||
| chr13:44515763
|
G | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+57400C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44515763 | ||||||
| chr13:44516178
|
G | T | 14 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+56985C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44516178 | ||||||
| chr13:44516242
|
G | C | 1 | a0001c0015t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2912+56921C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44516242 | ||||||
| chr13:44516342
|
A | C | 101 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(98): Show | 101 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2912+56821T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44516342 | ||||||
| chr13:44516444
|
C | T | 235 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.2912+56719G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44516444 | ||||||
| chr13:44516508
|
C | G | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+56655G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44516508 | ||||||
| chr13:44517086
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2912+56077C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517086 | ||||||
| chr13:44517094
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2912+56069A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517094 | ||||||
| chr13:44517098
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2912+56065C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517098 | ||||||
| chr13:44517317
|
G | A | 4 | a0001c0005t0004g0238a0001c0005t0004g0240a0001c0006t0006g0003others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+55846C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517317 | ||||||
| chr13:44517333
|
A | AAC | 79 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.2912+55828_2912+55 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517333 | ||||||
| chr13:44517333
|
A | AACAC | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0034others(16): Show | 19 | HG00597.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2912+55826_2912+55 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517333 | ||||||
| chr13:44517333
|
A | AACACAC | 3 | a0001c0001t0002g0122a0001c0001t0002g0145a0004c0004t0007g0227 | 3 | HG00733.hp1 HG02148.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2912+55824_2912+55 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517333 | ||||||
| chr13:44517333
|
AAC | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0048others(3): Show | 6 | HG01496.hp1 HG02896.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+55828_2912+55 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517333 | ||||||
| chr13:44517333
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0015g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2912+55820_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517333 | ||||||
| chr13:44517361
|
A | C | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+55802T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517361 | ||||||
| chr13:44517363
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+55800A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517363 | ||||||
| chr13:44517437
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+55726G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517437 | ||||||
| chr13:44517518
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+55645A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517518 | ||||||
| chr13:44517572
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2912+55591G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517572 | ||||||
| chr13:44517761
|
G | GTATATAC others(11): Show |
90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(87): Show | 90 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2912+55401_2912+55 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517761 | ||||||
| chr13:44517761
|
G | GTATATAC others(13): Show |
2 | a0001c0001t0001g0020a0001c0001t0012g0185 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2912+55401_2912+55 others(26): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517761 | ||||||
| chr13:44517762
|
T | TATATACA others(9): Show |
3 | a0001c0001t0001g0097a0001c0001t0001g0098a0004c0004t0003g0223 | 3 | HG04199.hp1 NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2912+55400_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517762 | ||||||
| chr13:44517763
|
G | A | 96 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(93): Show | 96 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2912+55400C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517763 | ||||||
| chr13:44517765
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2912+55398T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517765 | ||||||
| chr13:44517774
|
T | C | 95 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(92): Show | 95 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2912+55389A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517774 | ||||||
| chr13:44517776
|
T | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+55387A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517776 | ||||||
| chr13:44517811
|
A | G | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+55352T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517811 | ||||||
| chr13:44517811
|
ATG | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0201 | 3 | HG00597.hp2 NA19010.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2912+55350_2912+55 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517811 | ||||||
| chr13:44517811
|
ATGTGTG | A | 6 | a0001c0001t0001g0159a0001c0001t0001g0190a0001c0001t0001g0196others(3): Show | 6 | HG01978.hp2 HG02735.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+55346_2912+55 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517811 | ||||||
| chr13:44517819
|
G | GTGTGTA | 76 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2912+55343_2912+55 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517819 | ||||||
| chr13:44517821
|
GTGTGTGT others(5): Show |
G | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2912+55330_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517821 | ||||||
| chr13:44517823
|
G | A | 14 | a0001c0001t0001g0207a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+55340C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517823 | ||||||
| chr13:44517823
|
G | GTA | 6 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+55339_2912+55 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517823 | ||||||
| chr13:44517823
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2912+55328_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517823 | ||||||
| chr13:44517823
|
GTGTGTGT others(9): Show |
G | 7 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0193others(4): Show | 7 | HG02080.hp1 HG02083.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+55324_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517823 | ||||||
| chr13:44517823
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2912+55322_2912+55 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517823 | ||||||
| chr13:44517825
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0207 | 2 | HG02970.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2912+55338C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517825 | ||||||
| chr13:44517825
|
GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+55328_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517825 | ||||||
| chr13:44517827
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG00597.hp2 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+55336C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517827 | ||||||
| chr13:44517827
|
G | GTA | 4 | a0001c0001t0001g0160a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01516.hp1 HG04199.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+55335_2912+55 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517827 | ||||||
| chr13:44517827
|
G | GTATA | 11 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG02886.hp2 HG02897.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.2912+55335_2912+55 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517827 | ||||||
| chr13:44517829
|
G | A | 39 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(36): Show | 39 | HG00597.hp2 HG00639.hp2 HG01516.hp1 others(36): Show |
intron_variant | MODIFIER | c.2912+55334C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTATATA | 12 | a0001c0001t0001g0106a0001c0001t0002g0102a0001c0001t0002g0105others(9): Show | 12 | HG00735.hp2 HG01943.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.2912+55328_2912+55 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTATATAT others(1): Show |
11 | a0001c0001t0001g0044a0001c0001t0001g0121a0001c0001t0002g0103others(8): Show | 11 | HG00597.hp1 HG00639.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2912+55326_2912+55 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0083a0001c0001t0002g0144others(1): Show | 4 | HG02683.hp2 HG03486.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+55324_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0139others(1): Show | 4 | HG01109.hp2 HG02273.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+55322_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0002g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2912+55320_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0002g0181 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2912+55333_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517829
|
G | GTGTGTAT others(13): Show |
1 | a0007c0009t0002g0014 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2912+55333_2912+55 others(26): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517829 | ||||||
| chr13:44517831
|
A | G | 3 | a0001c0001t0002g0124a0001c0001t0002g0129a0003c0003t0003g0218 | 3 | HG02004.hp2 HG02027.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2912+55332T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517831 | ||||||
| chr13:44517847
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2912+55295_2912+55 others(27): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517847 | ||||||
| chr13:44517855
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0049 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2912+55307_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517855 | ||||||
| chr13:44517855
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2912+55307_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517855 | ||||||
| chr13:44517857
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(27): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0140a0001c0015t0002g0230a0010c0012t0020g0231 | 3 | NA18942.hp1 NA18948.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0064 | 2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0080a0001c0001t0013g0063a0001c0001t0017g0066 | 3 | HG00323.hp2 HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(25): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0097 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0098 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0065 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(23): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0078a0009c0008t0001g0013 | 2 | HG03654.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(25): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0188 | 2 | HG02080.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(26): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0056others(1): Show | 4 | HG02083.hp2 NA18948.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0016 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0086others(2): Show | 5 | HG02293.hp2 HG02622.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00673.hp2 NA18954.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0153a0001c0001t0001g0187 | 3 | HG01256.hp1 HG01258.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(23): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATT | 6 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(3): Show | 6 | HG00544.hp1 HG01255.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(3): Show |
1 | a0001c0001t0018g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(4): Show |
2 | a0001c0001t0001g0079a0004c0004t0003g0224 | 2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0012g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(6): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0099 | 3 | HG01109.hp1 HG03704.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(7): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0093 | 3 | HG01928.hp1 HG02027.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0045a0001c0001t0001g0184 | 3 | HG01243.hp2 HG01516.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATATTT others(9): Show |
1 | a0001c0001t0001g0026 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0154 | 2 | HG01070.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2912+55305_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(6): Show |
9 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0082others(6): Show | 9 | HG00544.hp2 HG02132.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(7): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(8): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0054 | 2 | HG01346.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATATTTTT others(9): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0068 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2912+55305_2912+55 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT | 6 | a0003c0003t0003g0217a0003c0003t0003g0218a0003c0003t0003g0221others(3): Show | 6 | HG00733.hp1 HG01943.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+55299_2912+55 others(13): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2912+55296_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0014g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2912+55295_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0069 | 2 | NA18942.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2912+55294_2912+55 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02074.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2912+55293_2912+55 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0095a0001c0001t0008g0234 | 2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2912+55292_2912+55 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
A | T | 14 | a0001c0001t0001g0049a0001c0001t0001g0090a0001c0001t0001g0158others(11): Show | 14 | HG00323.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+55306T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517857
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0193others(4): Show | 7 | HG02080.hp1 HG02083.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+55296_2912+55 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517857 | ||||||
| chr13:44517858
|
T | TATATATA | 3 | a0001c0001t0002g0142a0001c0001t0002g0148a0001c0001t0002g0156 | 3 | HG01070.hp1 HG03654.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2912+55304_2912+55 others(13): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517858 | ||||||
| chr13:44517858
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0002g0027 | 3 | HG03225.hp2 HG03579.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2912+55304_2912+55 others(15): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517858 | ||||||
| chr13:44517858
|
T | TATATATA others(4): Show |
1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+55304_2912+55 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517858 | ||||||
| chr13:44517859
|
T | A | 42 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0044others(39): Show | 42 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.2912+55304A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517859 | ||||||
| chr13:44517860
|
T | A | 3 | a0001c0001t0001g0166a0001c0001t0002g0027a0001c0001t0002g0208 | 3 | NA18955.hp1 NA18966.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2912+55303A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517860 | ||||||
| chr13:44517861
|
T | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0159a0001c0001t0001g0168others(12): Show | 15 | HG00597.hp2 HG00639.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.2912+55302A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517861 | ||||||
| chr13:44517862
|
T | A | 2 | a0001c0001t0001g0200a0001c0001t0002g0027 | 2 | NA18941.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2912+55301A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517862 | ||||||
| chr13:44517863
|
T | A | 8 | a0001c0001t0001g0159a0001c0001t0001g0196a0001c0001t0001g0198others(5): Show | 8 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2912+55300A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517863 | ||||||
| chr13:44517865
|
T | A | 5 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG02735.hp1 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+55298A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517865 | ||||||
| chr13:44517867
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2912+55296A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517867 | ||||||
| chr13:44517984
|
G | C | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+55179C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44517984 | ||||||
| chr13:44518718
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2912+54445G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44518718 | ||||||
| chr13:44518727
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2912+54436A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44518727 | ||||||
| chr13:44519089
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2912+54074G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519089 | ||||||
| chr13:44519223
|
T | C | 14 | a0001c0014t0003g0229a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+53940A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519223 | ||||||
| chr13:44519334
|
A | G | 120 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2912+53829T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519334 | ||||||
| chr13:44519845
|
T | C | 237 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2912+53318A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519845 | ||||||
| chr13:44519865
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.2912+53298T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519865 | ||||||
| chr13:44519876
|
T | C | 24 | a0001c0001t0002g0122a0001c0001t0002g0139a0001c0001t0002g0147others(21): Show | 24 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.2912+53287A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44519876 | ||||||
| chr13:44520007
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 4 | HG01256.hp2 HG01978.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+53156C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520007 | ||||||
| chr13:44520107
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2912+53056G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520107 | ||||||
| chr13:44520217
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2912+52946C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520217 | ||||||
| chr13:44520239
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2912+52924C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520239 | ||||||
| chr13:44520246
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2912+52917T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520246 | ||||||
| chr13:44520311
|
G | A | 26 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(23): Show | 26 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2912+52852C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520311 | ||||||
| chr13:44520365
|
T | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+52798A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520365 | ||||||
| chr13:44520575
|
TAA | T | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+52586_2912+52 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520575 | ||||||
| chr13:44520592
|
T | C | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+52571A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44520592 | ||||||
| chr13:44521208
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+51955C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521208 | ||||||
| chr13:44521580
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+51583A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521580 | ||||||
| chr13:44521596
|
T | C | 2 | a0001c0001t0011g0039a0001c0001t0018g0084 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2912+51567A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521596 | ||||||
| chr13:44521682
|
G | GA | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+51480dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521682 | ||||||
| chr13:44521682
|
GA | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+51480delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521682 | ||||||
| chr13:44521740
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2912+51423A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521740 | ||||||
| chr13:44521763
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0078 | 3 | HG02683.hp1 HG03710.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2912+51400C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521763 | ||||||
| chr13:44521769
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2912+51394A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521769 | ||||||
| chr13:44521784
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+51379G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521784 | ||||||
| chr13:44521950
|
T | TA | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+51212dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44521950 | ||||||
| chr13:44522253
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2912+50910T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522253 | ||||||
| chr13:44522344
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+50819T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522344 | ||||||
| chr13:44522657
|
C | A | 2 | a0001c0001t0011g0039a0001c0001t0018g0084 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2912+50506G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522657 | ||||||
| chr13:44522816
|
A | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0130 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2912+50347T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522816 | ||||||
| chr13:44522826
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0081 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2912+50337G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522826 | ||||||
| chr13:44522925
|
T | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG00558.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+50238A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44522925 | ||||||
| chr13:44523035
|
G | GA | 10 | a0001c0001t0001g0204a0001c0006t0006g0003a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.2912+50127dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44523035 | ||||||
| chr13:44523144
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2912+50019T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44523144 | ||||||
| chr13:44523435
|
A | C | 4 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+49728T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44523435 | ||||||
| chr13:44523835
|
C | T | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+49328G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44523835 | ||||||
| chr13:44523889
|
T | C | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+49274A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44523889 | ||||||
| chr13:44524054
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2912+49109G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44524054 | ||||||
| chr13:44524154
|
C | G | 1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+49009G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44524154 | ||||||
| chr13:44524252
|
C | T | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2912+48911G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44524252 | ||||||
| chr13:44524538
|
C | G | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+48625G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44524538 | ||||||
| chr13:44525088
|
C | T | 55 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2912+48075G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525088 | ||||||
| chr13:44525222
|
T | C | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+47941A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525222 | ||||||
| chr13:44525233
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2912+47930G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525233 | ||||||
| chr13:44525405
|
G | A | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+47758C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525405 | ||||||
| chr13:44525428
|
T | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG00558.hp2 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+47735A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525428 | ||||||
| chr13:44525489
|
T | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(5): Show | 8 | HG01516.hp2 HG01517.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+47674A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525489 | ||||||
| chr13:44525711
|
C | T | 1 | a0001c0014t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2912+47452G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525711 | ||||||
| chr13:44525729
|
A | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+47434T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525729 | ||||||
| chr13:44525795
|
C | CA | 12 | a0001c0001t0001g0098a0001c0001t0001g0158a0001c0001t0001g0169others(9): Show | 12 | HG01192.hp2 HG01243.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.2912+47367dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525795 | ||||||
| chr13:44525795
|
CA | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0058others(6): Show | 9 | HG00323.hp2 HG00673.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+47367delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525795 | ||||||
| chr13:44525795
|
CAA | C | 37 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0191others(34): Show | 37 | HG00597.hp2 HG01891.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.2912+47366_2912+47 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525795 | ||||||
| chr13:44525795
|
CAAA | C | 14 | a0002c0002t0001g0009a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+47365_2912+47 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525795 | ||||||
| chr13:44525812
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+47351T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525812 | ||||||
| chr13:44525886
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2912+47277C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525886 | ||||||
| chr13:44525917
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2912+47246G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525917 | ||||||
| chr13:44525996
|
C | G | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2912+47167G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44525996 | ||||||
| chr13:44526144
|
C | T | 2 | a0001c0005t0004g0238a0001c0005t0004g0240 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2912+47019G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44526144 | ||||||
| chr13:44526543
|
T | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2912+46620A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44526543 | ||||||
| chr13:44526612
|
C | T | 69 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0182others(66): Show | 69 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2912+46551G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44526612 | ||||||
| chr13:44526983
|
G | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0173 | 2 | NA18967.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.2912+46180C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44526983 | ||||||
| chr13:44527076
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2912+46087G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44527076 | ||||||
| chr13:44527081
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2912+46082G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44527081 | ||||||
| chr13:44527218
|
G | A | 9 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+45945C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44527218 | ||||||
| chr13:44527480
|
A | G | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+45683T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44527480 | ||||||
| chr13:44527993
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2912+45170T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44527993 | ||||||
| chr13:44528111
|
C | T | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+45052G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528111 | ||||||
| chr13:44528194
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2912+44969C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528194 | ||||||
| chr13:44528452
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2912+44711G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528452 | ||||||
| chr13:44528494
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+44669A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528494 | ||||||
| chr13:44528729
|
T | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+44434A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528729 | ||||||
| chr13:44528993
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0153 | 3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2912+44170G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44528993 | ||||||
| chr13:44529071
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2912+44092G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529071 | ||||||
| chr13:44529271
|
T | C | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+43892A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529271 | ||||||
| chr13:44529304
|
A | G | 1 | a0004c0004t0003g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2912+43859T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529304 | ||||||
| chr13:44529434
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+43729C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529434 | ||||||
| chr13:44529663
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+43500A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529663 | ||||||
| chr13:44529817
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2912+43346A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44529817 | ||||||
| chr13:44530212
|
C | T | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+42951G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530212 | ||||||
| chr13:44530465
|
CAG | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+42696_2912+42 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530465 | ||||||
| chr13:44530529
|
C | T | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2912+42634G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530529 | ||||||
| chr13:44530663
|
C | CA | 37 | a0001c0001t0001g0153a0001c0001t0001g0177a0001c0001t0001g0186others(34): Show | 37 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2912+42499dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530663 | ||||||
| chr13:44530829
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2912+42334G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530829 | ||||||
| chr13:44530834
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2912+42329A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530834 | ||||||
| chr13:44530915
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+42248G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44530915 | ||||||
| chr13:44531015
|
G | C | 19 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(16): Show | 19 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+42148C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531015 | ||||||
| chr13:44531269
|
T | C | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+41894A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531269 | ||||||
| chr13:44531392
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+41771C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531392 | ||||||
| chr13:44531450
|
A | C | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+41713T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531450 | ||||||
| chr13:44531502
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+41661G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531502 | ||||||
| chr13:44531529
|
AATAT | A | 13 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(10): Show | 13 | HG00673.hp2 HG01928.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+41630_2912+41 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531529 | ||||||
| chr13:44531581
|
G | GTTCTT | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+41577_2912+41 others(11): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531581 | ||||||
| chr13:44531584
|
C | G | 4 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+41579G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531584 | ||||||
| chr13:44531739
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0012g0185 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2912+41424C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531739 | ||||||
| chr13:44531777
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+41386G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531777 | ||||||
| chr13:44531882
|
T | C | 208 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2912+41281A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531882 | ||||||
| chr13:44531947
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0178 | 2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2912+41216T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531947 | ||||||
| chr13:44531951
|
T | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+41212A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44531951 | ||||||
| chr13:44532063
|
G | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+41100C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532063 | ||||||
| chr13:44532174
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2912+40989G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532174 | ||||||
| chr13:44532226
|
G | A | 4 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+40937C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532226 | ||||||
| chr13:44532375
|
A | G | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+40788T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532375 | ||||||
| chr13:44532403
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2912+40760G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532403 | ||||||
| chr13:44532460
|
G | A | 27 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(24): Show | 27 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.2912+40703C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532460 | ||||||
| chr13:44532476
|
C | CAAAATCT others(6): Show |
1 | a0001c0001t0001g0051 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2912+40674_2912+40 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532476 | ||||||
| chr13:44532482
|
CT | C | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+40680delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532482 | ||||||
| chr13:44532539
|
C | T | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+40624G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532539 | ||||||
| chr13:44532634
|
C | T | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+40529G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532634 | ||||||
| chr13:44532660
|
C | G | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+40503G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532660 | ||||||
| chr13:44532857
|
T | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0087others(2): Show | 5 | HG02027.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+40306A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532857 | ||||||
| chr13:44532904
|
C | G | 4 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+40259G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532904 | ||||||
| chr13:44532945
|
G | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+40218C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44532945 | ||||||
| chr13:44533010
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2912+40153T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533010 | ||||||
| chr13:44533042
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+40121G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533042 | ||||||
| chr13:44533197
|
C | G | 37 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(34): Show | 37 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2912+39966G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533197 | ||||||
| chr13:44533212
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+39951T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533212 | ||||||
| chr13:44533258
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+39905G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533258 | ||||||
| chr13:44533274
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+39889T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533274 | ||||||
| chr13:44533357
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2912+39806C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533357 | ||||||
| chr13:44533409
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02056.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2912+39754C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533409 | ||||||
| chr13:44533467
|
T | TA | 20 | a0001c0001t0001g0078a0001c0001t0001g0207a0001c0001t0004g0235others(17): Show | 20 | HG02257.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.2912+39695dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533467 | ||||||
| chr13:44533478
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2912+39685T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533478 | ||||||
| chr13:44533572
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2912+39591A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533572 | ||||||
| chr13:44533764
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2912+39399A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533764 | ||||||
| chr13:44533989
|
C | T | 4 | a0004c0004t0003g0223a0004c0004t0003g0226a0004c0004t0007g0227others(1): Show | 4 | HG00733.hp1 HG01981.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+39174G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44533989 | ||||||
| chr13:44534168
|
G | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02074.hp2 HG03710.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+38995C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534168 | ||||||
| chr13:44534205
|
G | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+38958C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534205 | ||||||
| chr13:44534231
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+38932C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534231 | ||||||
| chr13:44534231
|
G | GA | 9 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0087others(6): Show | 9 | HG02027.hp1 HG02027.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+38931dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534231 | ||||||
| chr13:44534231
|
G | GAA | 9 | a0001c0006t0006g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+38930_2912+38 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534231 | ||||||
| chr13:44534231
|
GA | G | 22 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0004g0235others(19): Show | 22 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.2912+38931delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534231 | ||||||
| chr13:44534361
|
T | TA | 16 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0087others(13): Show | 16 | HG02027.hp1 HG02027.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2912+38801dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534361 | ||||||
| chr13:44534361
|
TA | T | 22 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0061others(19): Show | 22 | HG00639.hp2 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.2912+38801delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534361 | ||||||
| chr13:44534361
|
TAA | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+38800_2912+38 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534361 | ||||||
| chr13:44534371
|
A | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0172others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+38792T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534371 | ||||||
| chr13:44534451
|
G | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+38712C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534451 | ||||||
| chr13:44534699
|
C | T | 6 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG02080.hp1 HG02083.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+38464G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44534699 | ||||||
| chr13:44535009
|
A | G | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+38154T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44535009 | ||||||
| chr13:44535621
|
A | AAAAC | 31 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0207others(28): Show | 31 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2912+37538_2912+37 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44535621 | ||||||
| chr13:44535621
|
AAAAC | A | 19 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(16): Show | 19 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+37538_2912+37 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44535621 | ||||||
| chr13:44535625
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2912+37538G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44535625 | ||||||
| chr13:44535997
|
T | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+37166A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44535997 | ||||||
| chr13:44536001
|
A | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0087others(2): Show | 5 | HG02027.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+37162T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536001 | ||||||
| chr13:44536138
|
C | A | 1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2912+37025G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536138 | ||||||
| chr13:44536320
|
C | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+36843G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536320 | ||||||
| chr13:44536490
|
A | T | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+36673T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536490 | ||||||
| chr13:44536553
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2912+36610T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536553 | ||||||
| chr13:44536926
|
GA | G | 117 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2912+36236delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAA | G | 15 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0062others(12): Show | 15 | HG00597.hp2 HG01074.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2912+36235_2912+36 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAA | G | 19 | a0001c0001t0001g0099a0001c0001t0001g0189a0001c0001t0001g0190others(16): Show | 19 | HG01975.hp2 HG01978.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.2912+36234_2912+36 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAA | G | 18 | a0001c0001t0008g0233a0001c0005t0004g0240a0001c0005t0009g0239others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+36233_2912+36 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAAA | G | 9 | a0001c0005t0009g0237a0001c0006t0006g0003a0002c0002t0001g0004others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+36232_2912+36 others(11): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2912+36225_2912+36 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAAAAA others(6): Show |
G | 2 | a0001c0001t0001g0051a0001c0001t0001g0173 | 2 | NA18967.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2912+36224_2912+36 others(19): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAAAAA others(7): Show |
G | 18 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0001g0169others(15): Show | 18 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+36223_2912+36 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536926
|
GAAAAAAA others(8): Show |
G | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+36222_2912+36 others(21): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536926 | ||||||
| chr13:44536938
|
A | C | 1 | a0001c0001t0010g0126 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2912+36225T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536938 | ||||||
| chr13:44536942
|
A | C | 1 | a0001c0001t0015g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2912+36221T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536942 | ||||||
| chr13:44536944
|
A | C | 1 | a0003c0003t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2912+36219T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536944 | ||||||
| chr13:44536945
|
A | C | 34 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0189others(31): Show | 34 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2912+36218T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536945 | ||||||
| chr13:44536948
|
A | C | 78 | a0001c0001t0001g0023a0001c0001t0001g0056a0001c0001t0001g0088others(75): Show | 78 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2912+36215T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536948 | ||||||
| chr13:44536951
|
A | C | 1 | a0001c0005t0009g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2912+36212T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536951 | ||||||
| chr13:44536954
|
A | C | 198 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.2912+36209T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44536954 | ||||||
| chr13:44537113
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2912+36050C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44537113 | ||||||
| chr13:44537925
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2912+35238T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44537925 | ||||||
| chr13:44538122
|
G | A | 1 | a0001c0014t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2912+35041C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44538122 | ||||||
| chr13:44538293
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2912+34870A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44538293 | ||||||
| chr13:44538411
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2912+34752A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44538411 | ||||||
| chr13:44538421
|
C | CA | 6 | a0001c0001t0001g0041a0001c0001t0001g0091a0001c0001t0001g0098others(3): Show | 6 | HG02027.hp2 HG03486.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+34741dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44538421 | ||||||
| chr13:44538693
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01167.hp2 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+34470T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44538693 | ||||||
| chr13:44539667
|
T | C | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+33496A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44539667 | ||||||
| chr13:44539716
|
A | AGG | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+33445_2912+33 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44539716 | ||||||
| chr13:44540249
|
A | G | 1 | a0001c0015t0002g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2912+32914T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44540249 | ||||||
| chr13:44540345
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2912+32818G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44540345 | ||||||
| chr13:44540882
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2912+32281A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44540882 | ||||||
| chr13:44541021
|
G | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+32142C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541021 | ||||||
| chr13:44541082
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+32081T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541082 | ||||||
| chr13:44541170
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2912+31993G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541170 | ||||||
| chr13:44541183
|
C | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+31980G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541183 | ||||||
| chr13:44541329
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00597.hp1 NA18954.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+31834C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541329 | ||||||
| chr13:44541666
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0002g0037 | 2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2912+31497C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541666 | ||||||
| chr13:44541673
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2912+31490C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541673 | ||||||
| chr13:44541680
|
G | A | 1 | a0001c0010t0002g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2912+31483C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541680 | ||||||
| chr13:44541912
|
T | C | 3 | a0001c0001t0002g0112a0001c0001t0002g0117a0001c0001t0002g0155 | 3 | HG01074.hp1 HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2912+31251A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541912 | ||||||
| chr13:44541926
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0094 | 2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2912+31237T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541926 | ||||||
| chr13:44541996
|
A | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+31167T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44541996 | ||||||
| chr13:44542191
|
C | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0006g0047 | 3 | HG01496.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2912+30972G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44542191 | ||||||
| chr13:44542475
|
A | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+30688T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44542475 | ||||||
| chr13:44542872
|
A | G | 2 | a0001c0001t0011g0039a0001c0001t0018g0084 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2912+30291T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44542872 | ||||||
| chr13:44542932
|
G | C | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+30231C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44542932 | ||||||
| chr13:44543147
|
C | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+30016G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44543147 | ||||||
| chr13:44543196
|
G | A | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2912+29967C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44543196 | ||||||
| chr13:44543608
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0081 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2912+29555C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44543608 | ||||||
| chr13:44544071
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+29092A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544071 | ||||||
| chr13:44544333
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | NA18952.hp2 NA18966.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+28830A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544333 | ||||||
| chr13:44544356
|
C | CA | 6 | a0001c0001t0001g0034a0001c0001t0001g0159a0001c0001t0002g0113others(3): Show | 6 | HG01433.hp1 HG02683.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+28806dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544356 | ||||||
| chr13:44544395
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2912+28768T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544395 | ||||||
| chr13:44544400
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2912+28763T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544400 | ||||||
| chr13:44544516
|
T | C | 1 | a0003c0003t0003g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2912+28647A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544516 | ||||||
| chr13:44544543
|
TA | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0194a0001c0001t0001g0206others(9): Show | 12 | HG00558.hp2 HG02615.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.2912+28619delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544543 | ||||||
| chr13:44544544
|
A | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+28619T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544544 | ||||||
| chr13:44544726
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2912+28437T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44544726 | ||||||
| chr13:44545135
|
G | T | 3 | a0001c0001t0001g0068a0001c0001t0002g0181a0006c0011t0002g0215 | 3 | HG01256.hp2 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2912+28028C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545135 | ||||||
| chr13:44545226
|
G | T | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+27937C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545226 | ||||||
| chr13:44545236
|
G | C | 1 | a0001c0001t0002g0181 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2912+27927C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545236 | ||||||
| chr13:44545249
|
C | T | 12 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(9): Show | 12 | HG01109.hp2 HG02074.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.2912+27914G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545249 | ||||||
| chr13:44545582
|
G | GA | 9 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0172others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+27580dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545582 | ||||||
| chr13:44545583
|
A | G | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+27580T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545583 | ||||||
| chr13:44545747
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0002g0148a0001c0001t0002g0149 | 3 | HG02056.hp2 NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2912+27416G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545747 | ||||||
| chr13:44545887
|
G | C | 1 | a0003c0003t0003g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2912+27276C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545887 | ||||||
| chr13:44545901
|
C | G | 1 | a0001c0010t0002g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2912+27262G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545901 | ||||||
| chr13:44545976
|
C | CA | 18 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(15): Show | 18 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.2912+27186dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545976 | ||||||
| chr13:44545984
|
A | T | 39 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(36): Show | 39 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(36): Show |
intron_variant | MODIFIER | c.2912+27179T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545984 | ||||||
| chr13:44545987
|
AT | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+27175delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545987 | ||||||
| chr13:44545988
|
T | A | 14 | a0001c0001t0002g0156a0003c0003t0003g0216a0003c0003t0003g0217others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+27175A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44545988 | ||||||
| chr13:44546220
|
G | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+26943C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546220 | ||||||
| chr13:44546274
|
T | C | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+26889A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546274 | ||||||
| chr13:44546356
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2912+26807G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546356 | ||||||
| chr13:44546749
|
C | CGT | 178 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2912+26412_2912+26 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGT | 25 | a0001c0001t0001g0038a0001c0001t0001g0173a0001c0001t0001g0178others(22): Show | 25 | HG00597.hp2 HG01070.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.2912+26410_2912+26 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGT | 9 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG01496.hp1 HG01975.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+26408_2912+26 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(1): Show |
7 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(4): Show | 7 | HG02615.hp2 HG02886.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+26406_2912+26 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0206 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2912+26404_2912+26 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(5): Show |
2 | a0002c0002t0001g0007a0002c0002t0001g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2912+26402_2912+26 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(9): Show |
1 | a0003c0003t0003g0219 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2912+26398_2912+26 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2912+26396_2912+26 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(13): Show |
2 | a0001c0001t0012g0185a0004c0004t0007g0227 | 2 | HG00733.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2912+26394_2912+26 others(26): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(15): Show |
8 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(5): Show | 8 | HG00323.hp1 HG01981.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+26392_2912+26 others(28): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(17): Show |
1 | a0003c0003t0003g0221 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2912+26390_2912+26 others(30): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
C | CGTGTGTG others(19): Show |
2 | a0004c0004t0001g0225a0004c0004t0003g0223 | 2 | HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2912+26388_2912+26 others(32): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44546749
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2912+26402_2912+26 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44546749 | ||||||
| chr13:44547380
|
A | G | 2 | a0001c0001t0001g0205a0005c0007t0001g0012 | 2 | HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2912+25783T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547380 | ||||||
| chr13:44547532
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+25631A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547532 | ||||||
| chr13:44547572
|
TCTC | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+25588_2912+25 others(9): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547572 | ||||||
| chr13:44547671
|
C | G | 152 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2912+25492G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547671 | ||||||
| chr13:44547767
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+25396A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547767 | ||||||
| chr13:44547875
|
G | A | 1 | a0001c0001t0014g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2912+25288C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44547875 | ||||||
| chr13:44548337
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2912+24826G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44548337 | ||||||
| chr13:44548509
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2912+24654A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44548509 | ||||||
| chr13:44548735
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+24428C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44548735 | ||||||
| chr13:44549094
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+24069A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549094 | ||||||
| chr13:44549107
|
A | G | 47 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(44): Show | 47 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2912+24056T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549107 | ||||||
| chr13:44549109
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0002g0104 | 2 | NA18966.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2912+24054A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549109 | ||||||
| chr13:44549130
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2912+24033C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549130 | ||||||
| chr13:44549286
|
T | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+23877A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549286 | ||||||
| chr13:44549559
|
G | C | 1 | a0003c0003t0003g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2912+23604C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549559 | ||||||
| chr13:44549779
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+23384T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549779 | ||||||
| chr13:44549801
|
G | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+23362C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549801 | ||||||
| chr13:44549802
|
C | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+23361G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549802 | ||||||
| chr13:44549831
|
C | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+23332G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549831 | ||||||
| chr13:44549842
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2912+23321C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549842 | ||||||
| chr13:44549854
|
T | C | 2 | a0001c0005t0009g0237a0001c0005t0009g0239 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2912+23309A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549854 | ||||||
| chr13:44549970
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2912+23193G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44549970 | ||||||
| chr13:44550380
|
G | A | 65 | a0001c0001t0001g0106a0001c0001t0001g0182a0001c0001t0001g0184others(62): Show | 65 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2912+22783C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550380 | ||||||
| chr13:44550450
|
C | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+22713G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550450 | ||||||
| chr13:44550586
|
GA | G | 55 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2912+22576delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550586 | ||||||
| chr13:44550635
|
C | T | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+22528G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550635 | ||||||
| chr13:44550722
|
C | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+22441G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550722 | ||||||
| chr13:44550835
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2912+22328C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550835 | ||||||
| chr13:44550939
|
CA | C | 19 | a0001c0001t0001g0020a0001c0001t0001g0086a0001c0001t0001g0186others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2912+22223delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44550939 | ||||||
| chr13:44551220
|
A | G | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+21943T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551220 | ||||||
| chr13:44551306
|
T | TGG | 15 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(12): Show | 15 | HG00544.hp1 HG01192.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.2912+21855_2912+21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551306 | ||||||
| chr13:44551310
|
G | GGGGTGTG others(3): Show |
1 | a0001c0005t0009g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2912+21852_2912+21 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGGGTGTG others(5): Show |
1 | a0001c0005t0009g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2912+21852_2912+21 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGT | 70 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0085others(67): Show | 70 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2912+21851_2912+21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGTGT | 14 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0050others(11): Show | 14 | HG00597.hp2 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2912+21849_2912+21 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGTGTGT | 5 | a0003c0003t0003g0216a0003c0003t0003g0218a0003c0003t0003g0219others(2): Show | 5 | HG01928.hp2 HG01943.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+21847_2912+21 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGTGTGTG others(1): Show |
10 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0234others(7): Show | 10 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.2912+21845_2912+21 others(14): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | GGTGTGTG others(3): Show |
4 | a0001c0001t0008g0233a0001c0001t0012g0185a0001c0005t0004g0238others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+21843_2912+21 others(16): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
G | T | 8 | a0001c0001t0001g0173a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG01346.hp2 NA18952.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+21853C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551310
|
GGT | G | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+21851_2912+21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551310 | ||||||
| chr13:44551312
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0003g0036 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2912+21851A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551312 | ||||||
| chr13:44551314
|
T | G | 9 | a0001c0006t0006g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+21849A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551314 | ||||||
| chr13:44551382
|
T | G | 1 | a0001c0001t0002g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2912+21781A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551382 | ||||||
| chr13:44551386
|
A | ATGGGTGG others(5): Show |
4 | a0004c0004t0001g0225a0004c0004t0003g0223a0004c0004t0003g0226others(1): Show | 4 | HG00733.hp1 HG01517.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+21776_2912+21 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551386 | ||||||
| chr13:44551389
|
G | GGT | 19 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0103others(16): Show | 19 | HG00558.hp1 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+21772_2912+21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(7): Show |
1 | a0004c0004t0003g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2912+21773_2912+21 others(20): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(11): Show |
4 | a0003c0003t0003g0219a0003c0003t0003g0220a0003c0003t0003g0221others(1): Show | 4 | HG00323.hp1 HG01928.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+21773_2912+21 others(24): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(15): Show |
1 | a0003c0003t0003g0216 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2912+21773_2912+21 others(28): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(10): Show |
1 | a0003c0003t0003g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2912+21773_2912+21 others(23): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(12): Show |
1 | a0003c0003t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2912+21773_2912+21 others(25): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGGGTG others(9): Show |
1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+21773_2912+21 others(22): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
G | GGTGTGT | 9 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0002g0115others(6): Show | 9 | HG00639.hp1 HG01516.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.2912+21768_2912+21 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
GGT | G | 57 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(54): Show | 57 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.2912+21772_2912+21 others(8): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
GGTGT | G | 29 | a0001c0001t0001g0023a0001c0001t0001g0085a0001c0001t0001g0086others(26): Show | 29 | HG00544.hp1 HG00597.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2912+21770_2912+21 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
GGTGTGT | G | 25 | a0001c0001t0001g0050a0001c0001t0001g0161a0001c0001t0001g0162others(22): Show | 25 | HG00639.hp2 HG01975.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.2912+21768_2912+21 others(12): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551389
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2912+21762_2912+21 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551389 | ||||||
| chr13:44551391
|
T | G | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2912+21772A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551391 | ||||||
| chr13:44551393
|
T | G | 13 | a0001c0001t0001g0191a0001c0001t0001g0207a0001c0005t0009g0237others(10): Show | 13 | HG01981.hp1 HG02080.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2912+21770A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551393 | ||||||
| chr13:44551395
|
T | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG01891.hp2 HG02083.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+21768A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551395 | ||||||
| chr13:44551397
|
T | G | 17 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(14): Show | 17 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2912+21766A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551397 | ||||||
| chr13:44551399
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0016g0192a0001c0005t0004g0238 | 3 | HG02083.hp1 HG02132.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2912+21764A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551399 | ||||||
| chr13:44551401
|
T | G | 17 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(14): Show | 17 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2912+21762A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551401 | ||||||
| chr13:44551403
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0016g0192 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2912+21760A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551403 | ||||||
| chr13:44551405
|
T | G | 16 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0194others(13): Show | 16 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.2912+21758A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551405 | ||||||
| chr13:44551425
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2912+21738A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551425 | ||||||
| chr13:44551467
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+21696G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551467 | ||||||
| chr13:44551530
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2912+21633G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551530 | ||||||
| chr13:44551752
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG02572.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2912+21411A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551752 | ||||||
| chr13:44551831
|
T | C | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+21332A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44551831 | ||||||
| chr13:44552339
|
A | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+20824T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552339 | ||||||
| chr13:44552449
|
A | T | 1 | a0001c0014t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2912+20714T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552449 | ||||||
| chr13:44552490
|
G | A | 56 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(53): Show | 56 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2912+20673C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552490 | ||||||
| chr13:44552583
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2912+20580C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552583 | ||||||
| chr13:44552635
|
A | G | 8 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(5): Show | 8 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+20528T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552635 | ||||||
| chr13:44552763
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+20400G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552763 | ||||||
| chr13:44552841
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+20322T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552841 | ||||||
| chr13:44552883
|
G | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG01109.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2912+20280C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552883 | ||||||
| chr13:44552976
|
C | A | 236 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(233): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.2912+20187G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552976 | ||||||
| chr13:44552988
|
A | AAAAC | 9 | a0001c0006t0006g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+20171_2912+20 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44552988 | ||||||
| chr13:44553346
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2912+19817A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44553346 | ||||||
| chr13:44553814
|
T | C | 11 | a0001c0001t0001g0207a0001c0006t0006g0003a0001c0006t0021g0232others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2912+19349A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44553814 | ||||||
| chr13:44553848
|
C | A | 1 | a0001c0001t0002g0137 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2912+19315G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44553848 | ||||||
| chr13:44553849
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+19314C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44553849 | ||||||
| chr13:44553873
|
G | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+19290C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44553873 | ||||||
| chr13:44554019
|
C | T | 1 | a0001c0001t0012g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2912+19144G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554019 | ||||||
| chr13:44554041
|
C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+19122G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554041 | ||||||
| chr13:44554085
|
C | T | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+19078G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554085 | ||||||
| chr13:44554146
|
A | G | 37 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(34): Show | 37 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2912+19017T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554146 | ||||||
| chr13:44554313
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2912+18850G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554313 | ||||||
| chr13:44554381
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2912+18782T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554381 | ||||||
| chr13:44554454
|
T | C | 2 | a0001c0001t0001g0205a0005c0007t0001g0012 | 2 | HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2912+18709A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554454 | ||||||
| chr13:44554630
|
C | CA | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0044others(16): Show | 19 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+18532dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554630 | ||||||
| chr13:44554630
|
CA | C | 15 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0001g0162others(12): Show | 15 | HG01943.hp1 HG02132.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2912+18532delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554630 | ||||||
| chr13:44554630
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+18524_2912+18 others(15): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554630 | ||||||
| chr13:44554630
|
CAAAAAAA others(4): Show |
C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+18522_2912+18 others(17): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554630 | ||||||
| chr13:44554630
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+18521_2912+18 others(18): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554630 | ||||||
| chr13:44554726
|
AT | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+18436delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554726 | ||||||
| chr13:44554769
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2912+18394T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554769 | ||||||
| chr13:44554943
|
A | C | 18 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(15): Show | 18 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.2912+18220T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554943 | ||||||
| chr13:44554958
|
G | A | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+18205C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44554958 | ||||||
| chr13:44555010
|
T | C | 1 | a0001c0005t0009g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2912+18153A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555010 | ||||||
| chr13:44555011
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+18152T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555011 | ||||||
| chr13:44555118
|
T | TA | 24 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(21): Show | 24 | HG00597.hp2 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2912+18044dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555118 | ||||||
| chr13:44555118
|
TA | T | 9 | a0001c0001t0001g0153a0001c0001t0001g0179a0001c0001t0002g0108others(6): Show | 9 | HG00544.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+18044delT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555118 | ||||||
| chr13:44555191
|
T | C | 19 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(16): Show | 19 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+17972A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555191 | ||||||
| chr13:44555211
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+17952A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555211 | ||||||
| chr13:44555275
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+17888A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555275 | ||||||
| chr13:44555306
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0006g0047 | 3 | HG01496.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2912+17857T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555306 | ||||||
| chr13:44555342
|
G | T | 1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+17821C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555342 | ||||||
| chr13:44555353
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2912+17810T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555353 | ||||||
| chr13:44555475
|
G | A | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+17688C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555475 | ||||||
| chr13:44555584
|
C | T | 4 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+17579G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555584 | ||||||
| chr13:44555606
|
A | AAAAT | 18 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(15): Show | 18 | HG00597.hp2 HG01433.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.2912+17553_2912+17 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555606 | ||||||
| chr13:44555634
|
C | T | 19 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(16): Show | 19 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+17529G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555634 | ||||||
| chr13:44555670
|
G | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+17493C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555670 | ||||||
| chr13:44555742
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+17421T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44555742 | ||||||
| chr13:44556095
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2912+17068T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44556095 | ||||||
| chr13:44556124
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2912+17039A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44556124 | ||||||
| chr13:44556224
|
T | TA | 10 | a0001c0001t0001g0024a0001c0001t0001g0182a0001c0006t0006g0003others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.2912+16938dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44556224 | ||||||
| chr13:44556373
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2912+16790G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44556373 | ||||||
| chr13:44556798
|
G | A | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+16365C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44556798 | ||||||
| chr13:44557237
|
C | T | 1 | a0001c0001t0012g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2912+15926G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44557237 | ||||||
| chr13:44557379
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2912+15784A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44557379 | ||||||
| chr13:44557418
|
G | A | 6 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0005t0004g0238others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+15745C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44557418 | ||||||
| chr13:44557585
|
G | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+15578C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44557585 | ||||||
| chr13:44558048
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2912+15115C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558048 | ||||||
| chr13:44558217
|
T | A | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | NA18952.hp2 NA18966.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+14946A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558217 | ||||||
| chr13:44558300
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2912+14863A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558300 | ||||||
| chr13:44558328
|
T | C | 18 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(15): Show | 18 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.2912+14835A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558328 | ||||||
| chr13:44558348
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2912+14815A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558348 | ||||||
| chr13:44558409
|
C | T | 4 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(1): Show | 4 | HG00544.hp1 HG01255.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+14754G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558409 | ||||||
| chr13:44558602
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2912+14561A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558602 | ||||||
| chr13:44558863
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2912+14300G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44558863 | ||||||
| chr13:44559100
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | NA18954.hp1 NA18966.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2912+14063T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44559100 | ||||||
| chr13:44559693
|
C | CT | 62 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0040others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.2912+13469dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44559693 | ||||||
| chr13:44560168
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02056.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2912+12995C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44560168 | ||||||
| chr13:44560252
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2912+12911T>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44560252 | ||||||
| chr13:44560315
|
TG | T | 18 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+12847delC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44560315 | ||||||
| chr13:44560716
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2912+12447G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44560716 | ||||||
| chr13:44560772
|
C | G | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+12391G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44560772 | ||||||
| chr13:44561155
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2912+12008C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44561155 | ||||||
| chr13:44561315
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2912+11848G>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44561315 | ||||||
| chr13:44561393
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2912+11770T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44561393 | ||||||
| chr13:44561703
|
G | GTTAT | 11 | a0001c0001t0001g0207a0001c0006t0006g0003a0001c0006t0021g0232others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2912+11456_2912+11 others(10): Show |
TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44561703 | ||||||
| chr13:44561711
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+11452A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44561711 | ||||||
| chr13:44562100
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2912+11063G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562100 | ||||||
| chr13:44562312
|
A | AC | 9 | a0001c0006t0006g0003a0002c0002t0001g0004a0002c0002t0001g0005others(6): Show | 9 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2912+10850dupG | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562312 | ||||||
| chr13:44562506
|
C | T | 1 | a0001c0006t0006g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2912+10657G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562506 | ||||||
| chr13:44562721
|
T | C | 1 | a0001c0001t0015g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2912+10442A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562721 | ||||||
| chr13:44562782
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2912+10381A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562782 | ||||||
| chr13:44562904
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2912+10259C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562904 | ||||||
| chr13:44562962
|
G | A | 2 | a0001c0001t0001g0099a0006c0011t0002g0215 | 2 | HG01978.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2912+10201C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44562962 | ||||||
| chr13:44563002
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA18957.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2912+10161C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563002 | ||||||
| chr13:44563065
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2912+10098A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563065 | ||||||
| chr13:44563637
|
G | A | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+9526C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563637 | ||||||
| chr13:44563758
|
A | G | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+9405T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563758 | ||||||
| chr13:44563795
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+9368A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563795 | ||||||
| chr13:44563801
|
G | A | 17 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2912+9362C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563801 | ||||||
| chr13:44563882
|
T | G | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.2912+9281A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563882 | ||||||
| chr13:44563960
|
C | A | 36 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(33): Show | 36 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2912+9203G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44563960 | ||||||
| chr13:44564081
|
T | C | 6 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(3): Show | 6 | HG01928.hp2 HG01943.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+9082A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564081 | ||||||
| chr13:44564130
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2912+9033A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564130 | ||||||
| chr13:44564474
|
G | A | 18 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(15): Show | 18 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.2912+8689C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564474 | ||||||
| chr13:44564496
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2912+8667C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564496 | ||||||
| chr13:44564691
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2912+8472C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564691 | ||||||
| chr13:44564696
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2912+8467C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44564696 | ||||||
| chr13:44565010
|
T | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+8153A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44565010 | ||||||
| chr13:44565638
|
G | A | 2 | a0001c0001t0001g0205a0005c0007t0001g0012 | 2 | HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2912+7525C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44565638 | ||||||
| chr13:44565825
|
T | C | 13 | a0003c0003t0003g0216a0003c0003t0003g0217a0003c0003t0003g0218others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.2912+7338A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44565825 | ||||||
| chr13:44565981
|
T | G | 1 | a0001c0005t0009g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2912+7182A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44565981 | ||||||
| chr13:44567023
|
G | GA | 7 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2912+6139dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567023 | ||||||
| chr13:44567060
|
T | C | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+6103A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567060 | ||||||
| chr13:44567333
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2912+5830T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567333 | ||||||
| chr13:44567406
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2912+5757G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567406 | ||||||
| chr13:44567492
|
C | A | 67 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0182others(64): Show | 67 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2912+5671G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567492 | ||||||
| chr13:44567494
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2912+5669T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567494 | ||||||
| chr13:44567503
|
G | GA | 31 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(28): Show | 31 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.2912+5659dupT | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567503 | ||||||
| chr13:44567857
|
C | T | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+5306G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567857 | ||||||
| chr13:44567967
|
A | AG | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2912+5195dupC | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44567967 | ||||||
| chr13:44568070
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+5093A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568070 | ||||||
| chr13:44568072
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+5091C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568072 | ||||||
| chr13:44568074
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+5089T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568074 | ||||||
| chr13:44568194
|
C | A | 1 | a0001c0001t0015g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2912+4969G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568194 | ||||||
| chr13:44568656
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2912+4507A>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568656 | ||||||
| chr13:44568792
|
T | G | 1 | a0001c0014t0003g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2912+4371A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44568792 | ||||||
| chr13:44569169
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2912+3994T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44569169 | ||||||
| chr13:44569488
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2912+3675G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44569488 | ||||||
| chr13:44570030
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2912+3133A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570030 | ||||||
| chr13:44570075
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2912+3088G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570075 | ||||||
| chr13:44570188
|
C | CT | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG02074.hp1 HG02280.hp1 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.2912+2974dupA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570188 | ||||||
| chr13:44570188
|
CT | C | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+2974delA | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570188 | ||||||
| chr13:44570208
|
A | G | 37 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(34): Show | 37 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2912+2955T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570208 | ||||||
| chr13:44570351
|
T | C | 19 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(16): Show | 19 | HG00597.hp2 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.2912+2812A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570351 | ||||||
| chr13:44570574
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2912+2589A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570574 | ||||||
| chr13:44570672
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2912+2491T>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570672 | ||||||
| chr13:44570812
|
T | C | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+2351A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570812 | ||||||
| chr13:44570939
|
T | C | 1 | a0001c0006t0021g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2912+2224A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570939 | ||||||
| chr13:44570968
|
T | C | 27 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(24): Show | 27 | HG00639.hp2 HG01516.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.2912+2195A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44570968 | ||||||
| chr13:44571219
|
G | T | 18 | a0001c0001t0001g0020a0001c0001t0001g0186a0001c0001t0001g0187others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2912+1944C>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44571219 | ||||||
| chr13:44571471
|
G | C | 3 | a0001c0001t0001g0182a0001c0001t0002g0180a0001c0001t0002g0181 | 3 | HG01256.hp2 NA18990.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2912+1692C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44571471 | ||||||
| chr13:44571607
|
T | G | 1 | a0001c0005t0004g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2912+1556A>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44571607 | ||||||
| chr13:44572114
|
G | A | 10 | a0001c0006t0006g0003a0001c0006t0021g0232a0002c0002t0001g0004others(7): Show | 10 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2912+1049C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44572114 | ||||||
| chr13:44572230
|
C | A | 11 | a0001c0001t0001g0207a0001c0006t0006g0003a0001c0006t0021g0232others(8): Show | 11 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.2912+933G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44572230 | ||||||
| chr13:44572464
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0002g0183 | 2 | HG01243.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2912+699C>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44572464 | ||||||
| chr13:44572567
|
G | C | 8 | a0001c0001t0004g0235a0001c0001t0004g0236a0001c0001t0008g0233others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2912+596C>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44572567 | ||||||
| chr13:44572910
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG00558.hp2 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.2912+253G>A | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44572910 | ||||||
| chr13:44573052
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2912+111T>C | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44573052 | ||||||
| chr13:44573060
|
C | A | 55 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2912+103G>T | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44573060 | ||||||
| chr13:44573128
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | NA18952.hp2 NA18966.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2912+35A>G | TSC22D1 | ENSG00000102804.16 | transcript | ENST00000458659.3 | protein_coding | 1/2 | chr13 | 44573128 |