Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9194 |
|---|---|
| ensemblid | ENSG00000118596.12 |
| hgncid | 10928 |
| symbol | SLC16A7 |
| name | solute carrier family 16 member 7 |
| refseq_nuc | NM_001270623.2 |
| refseq_prot | NP_001257552.1 |
| ensembl_nuc | ENST00000547379.6 |
| ensembl_prot | ENSP00000448071.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 59596029 |
| end | 59789841 |
| strand | + |
| ver | v1.2 |
| region | chr12:59596029-59789841 |
| region5000 | chr12:59591029-59794841 |
| regionname0 | SLC16A7_chr12_59596029_59789841 |
| regionname5000 | SLC16A7_chr12_59591029_59794841 |
| 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 | 478 | 183 | 58 | 28 | 72 | 4 | 19 | 53 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002 | 0/0 | 478 | 69 | 16 | 8 | 34 | 2 | 9 | 23 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0003 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0004 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0005 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0006 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0007 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0008 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| 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 | 1437 | 164 | 55 | 27 | 67 | 4 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0002 | 0/0 | 1437 | 68 | 15 | 8 | 34 | 2 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0003 | 0/0 | 1437 | 19 | 3 | 1 | 5 | 0 | 10 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0004 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0005 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0006 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0007 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0008 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0009 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 10500 | 43 | 6 | 8 | 25 | 1 | 2 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0002 | 1/0 | 10500 | 42 | 6 | 7 | 21 | 2 | 5 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0003 | 0/0 | 10500 | 35 | 7 | 6 | 16 | 0 | 6 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0004 | 0/0 | 10500 | 23 | 2 | 1 | 16 | 1 | 3 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0005 | 0/0 | 10513 | 18 | 3 | 1 | 5 | 0 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0006 | 0/0 | 10515 | 15 | 14 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0007 | 0/0 | 10500 | 14 | 5 | 5 | 4 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0008 | 0/0 | 10500 | 6 | 5 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0009 | 0/0 | 10500 | 6 | 4 | 2 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0010 | 0/0 | 10500 | 4 | 0 | 2 | 1 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0011 | 0/0 | 10501 | 4 | 0 | 0 | 4 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0012 | 0/0 | 10519 | 4 | 4 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0013 | 0/0 | 10500 | 3 | 3 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0014 | 0/0 | 10500 | 3 | 0 | 0 | 3 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0015 | 0/0 | 10515 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0016 | 0/0 | 10500 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0017 | 0/0 | 10500 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0018 | 0/0 | 10500 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0019 | 0/0 | 10519 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0020 | 0/0 | 10514 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0021 | 0/0 | 10515 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0022 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0023 | 0/0 | 10500 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0024 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0025 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0026 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0027 | 0/0 | 10501 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0028 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0029 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0030 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0031 | 0/0 | 10500 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0032 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0033 | 0/0 | 10500 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0034 | 0/0 | 10500 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0035 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0036 | 0/0 | 10500 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0037 | 0/0 | 10500 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0038 | 0/0 | 10500 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0039 | 0/0 | 10500 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0040 | 0/0 | 10511 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0041 | 0/0 | 10503 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0042 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0043 | 0/0 | 10500 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0044 | 0/0 | 10500 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0045 | 0/0 | 10502 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0046 | 0/0 | 10502 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0047 | 0/0 | 10504 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| t0048 | 0/0 | 10516 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| 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 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| 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 | 1437 | 164 | 55 | 27 | 67 | 4 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0003 | 0/0 | 1437 | 19 | 3 | 1 | 5 | 0 | 10 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002 | 0/0 | 1437 | 68 | 15 | 8 | 34 | 2 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0006 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0003c0004 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0004c0005 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0005c0009 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0006c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0007c0008 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0008c0007 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 11936 | 43 | 6 | 8 | 25 | 1 | 2 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0002 | 1/0 | 11936 | 42 | 6 | 7 | 21 | 2 | 5 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0006 | 0/0 | 11951 | 15 | 14 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0007 | 0/0 | 11936 | 14 | 5 | 5 | 4 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0009 | 0/0 | 11936 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0010 | 0/0 | 11936 | 3 | 0 | 2 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0011 | 0/0 | 11937 | 4 | 0 | 0 | 4 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0012 | 0/0 | 11955 | 4 | 4 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0013 | 0/0 | 11936 | 3 | 3 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0014 | 0/0 | 11936 | 3 | 0 | 0 | 3 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0015 | 0/0 | 11951 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0018 | 0/0 | 11936 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0019 | 0/0 | 11955 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0020 | 0/0 | 11950 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0021 | 0/0 | 11951 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0025 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0026 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0027 | 0/0 | 11937 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0028 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0029 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0030 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0031 | 0/0 | 11936 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0032 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0033 | 0/0 | 11936 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0034 | 0/0 | 11936 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0035 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0036 | 0/0 | 11936 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0037 | 0/0 | 11936 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0038 | 0/0 | 11936 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0039 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0041 | 0/0 | 11939 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0042 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0043 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0044 | 0/0 | 11936 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0045 | 0/0 | 11938 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0046 | 0/0 | 11938 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0047 | 0/0 | 11940 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0001t0048 | 0/0 | 11952 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0003t0005 | 0/0 | 11949 | 18 | 3 | 1 | 5 | 0 | 9 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0001c0003t0010 | 0/0 | 11936 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0003 | 0/0 | 11936 | 33 | 7 | 6 | 14 | 0 | 6 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0004 | 0/0 | 11936 | 23 | 2 | 1 | 16 | 1 | 3 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0008 | 0/0 | 11936 | 6 | 5 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0016 | 0/0 | 11936 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0017 | 0/0 | 11936 | 2 | 0 | 0 | 2 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0023 | 0/0 | 11936 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0002t0024 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0002c0006t0022 | 0/0 | 11936 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0003c0004t0009 | 0/0 | 11936 | 2 | 0 | 2 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0004c0005t0009 | 0/0 | 11936 | 2 | 2 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0005c0009t0003 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0006c0010t0020 | 0/0 | 11950 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0007c0008t0040 | 0/0 | 11947 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| a0008c0007t0003 | 0/0 | 11936 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | copy fasta | chr12 | 59591029 | 59794841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0011g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0014g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0018g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0019g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0020g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0021g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0025g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0026g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0027g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0028g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0029g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0030g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0031g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0032g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0033g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0034g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0035g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0036g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0037g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0038g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0039g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0041g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0042g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0043g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0044g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0045g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0046g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0047g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0001t0048g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0001c0003t0010g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0016g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0017g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0023g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0002t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0002c0006t0022g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0003c0004t0009g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0003c0004t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0004c0005t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0004c0005t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0005c0009t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0006c0010t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0007c0008t0040g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| a0008c0007t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0023 | g0238 | EUR | GBR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00099 | hp2 | a0001 | c0001 | t0034 | g0084 | EUR | GBR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | GBR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00280 | hp1 | a0002 | c0002 | t0004 | g0040 | EUR | FIN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00438 | hp1 | a0002 | c0002 | t0004 | g0038 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0188 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0077 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00609 | hp1 | a0002 | c0002 | t0017 | g0182 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00621 | hp1 | a0001 | c0003 | t0005 | g0216 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00621 | hp2 | a0002 | c0002 | t0004 | g0099 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0123 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00673 | hp1 | a0001 | c0001 | t0035 | g0066 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00673 | hp2 | a0001 | c0001 | t0014 | g0023 | EAS | CHS | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0147 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0128 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0109 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0060 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0212 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0167 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01167 | hp1 | a0002 | c0002 | t0003 | g0149 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01167 | hp2 | a0003 | c0004 | t0009 | g0250 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01169 | hp1 | a0003 | c0004 | t0009 | g0249 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01169 | hp2 | a0001 | c0001 | t0031 | g0010 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01175 | hp1 | a0002 | c0002 | t0008 | g0257 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01175 | hp2 | a0001 | c0001 | t0033 | g0083 | AMR | PUR | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01261 | hp2 | a0001 | c0003 | t0005 | g0141 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01346 | hp2 | a0001 | c0001 | t0038 | g0062 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0214 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0103 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01496 | hp1 | a0001 | c0001 | t0044 | g0050 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0228 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01884 | hp2 | a0001 | c0003 | t0005 | g0075 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0170 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0064 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0070 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0201 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02071 | hp1 | a0001 | c0001 | t0011 | g0144 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02071 | hp2 | a0002 | c0002 | t0004 | g0142 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02080 | hp2 | a0001 | c0003 | t0005 | g0218 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02083 | hp1 | a0002 | c0002 | t0017 | g0174 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0085 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02145 | hp2 | a0001 | c0001 | t0048 | g0081 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02155 | hp2 | a0001 | c0001 | t0014 | g0211 | EAS | CDX | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02165 | hp1 | a0001 | c0003 | t0005 | g0012 | EAS | CDX | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02257 | hp1 | a0002 | c0002 | t0008 | g0088 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0166 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0031 | AMR | PEL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0259 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02572 | hp2 | a0006 | c0010 | t0020 | g0108 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02615 | hp2 | a0001 | c0001 | t0025 | g0248 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02630 | hp2 | a0001 | c0001 | t0041 | g0232 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02647 | hp1 | a0001 | c0001 | t0043 | g0047 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0114 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02683 | hp2 | a0001 | c0003 | t0005 | g0164 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02698 | hp2 | a0001 | c0003 | t0010 | g0019 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02723 | hp2 | a0001 | c0001 | t0047 | g0245 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02735 | hp2 | a0001 | c0003 | t0005 | g0007 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02809 | hp1 | a0001 | c0001 | t0019 | g0080 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02809 | hp2 | a0001 | c0001 | t0042 | g0252 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02886 | hp1 | a0001 | c0001 | t0021 | g0223 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0247 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0219 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02896 | hp1 | a0001 | c0001 | t0019 | g0242 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0111 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0258 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0076 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02976 | hp1 | a0004 | c0005 | t0009 | g0089 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02976 | hp2 | a0002 | c0002 | t0008 | g0227 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03017 | hp2 | a0001 | c0003 | t0005 | g0009 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03041 | hp1 | a0004 | c0005 | t0009 | g0233 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03098 | hp1 | a0002 | c0002 | t0008 | g0072 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03130 | hp1 | a0001 | c0001 | t0045 | g0013 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03139 | hp1 | a0001 | c0003 | t0005 | g0195 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0074 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03239 | hp1 | a0001 | c0001 | t0037 | g0154 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03239 | hp2 | a0001 | c0003 | t0005 | g0240 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03486 | hp1 | a0002 | c0002 | t0008 | g0206 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03486 | hp2 | a0002 | c0006 | t0022 | g0078 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03490 | hp1 | a0001 | c0003 | t0005 | g0235 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03490 | hp2 | a0001 | c0003 | t0005 | g0093 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03492 | hp1 | a0001 | c0003 | t0005 | g0236 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0190 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ESN | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0246 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03540 | hp2 | a0002 | c0002 | t0008 | g0251 | AFR | GWD | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03579 | hp2 | a0002 | c0002 | t0024 | g0034 | AFR | MSL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03669 | hp1 | a0001 | c0003 | t0005 | g0203 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0229 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0120 | SAS | PJL | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0239 | SAS | BEB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0231 | SAS | BEB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04199 | hp1 | a0002 | c0002 | t0004 | g0256 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0217 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04204 | hp2 | a0001 | c0001 | t0036 | g0241 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG04228 | hp2 | a0001 | c0003 | t0005 | g0116 | SAS | STU | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0006 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18747 | hp1 | a0001 | c0001 | t0027 | g0090 | EAS | CHB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0094 | EAS | CHB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0254 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18940 | hp2 | a0002 | c0002 | t0004 | g0138 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18951 | hp1 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18957 | hp1 | a0001 | c0001 | t0039 | g0115 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18957 | hp2 | a0002 | c0002 | t0004 | g0137 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0136 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18969 | hp1 | a0001 | c0001 | t0028 | g0133 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18969 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0052 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18971 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18973 | hp2 | a0002 | c0002 | t0016 | g0162 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0102 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0186 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18979 | hp1 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18981 | hp2 | a0001 | c0003 | t0005 | g0087 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18983 | hp1 | a0002 | c0002 | t0003 | g0156 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18984 | hp1 | a0001 | c0001 | t0018 | g0096 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18989 | hp1 | a0002 | c0002 | t0016 | g0165 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18989 | hp2 | a0001 | c0001 | t0029 | g0105 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0189 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19002 | hp1 | a0001 | c0003 | t0005 | g0091 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19002 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19007 | hp1 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19007 | hp2 | a0002 | c0002 | t0004 | g0230 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0181 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0169 | AFR | LWK | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19054 | hp2 | a0002 | c0002 | t0004 | g0092 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0192 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19062 | hp2 | a0008 | c0007 | t0003 | g0045 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19065 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19074 | hp1 | a0001 | c0001 | t0030 | g0018 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19074 | hp2 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19075 | hp2 | a0005 | c0009 | t0003 | g0187 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19079 | hp2 | a0001 | c0001 | t0026 | g0042 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19083 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19083 | hp2 | a0001 | c0001 | t0014 | g0145 | EAS | JPT | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | YRI | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ASW | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0244 | AFR | ASW | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | GIH | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0122 | SAS | GIH | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0237 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02559 | hp1 | a0001 | c0001 | t0046 | g0002 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0004 | AFR | ACB | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG06807 | hp1 | a0001 | c0001 | t0032 | g0234 | AFR | USA | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | USA | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | USA | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | USA | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA21309 | hp1 | a0007 | c0008 | t0040 | g0151 | AFR | LWK | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | LWK | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0044 | REF | REF | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0063 | REF | REF | SLC16A7_chr12_59591029_59794841 | SLC16A7 | chr12 | 59591029 | 59794841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:59774810
|
T | A | 1 | a0008 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.515T>A | p.Phe172Tyr | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/6 | 852/11936 | 515/1437 | 172/478 | chr12 | 59774810 | ||
| chr12:59774897
|
A | G | 1 | a0004 | 2 | HG02976.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.602A>G | p.Asn201Ser | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/6 | 939/11936 | 602/1437 | 201/478 | chr12 | 59774897 | ||
| chr12:59775190
|
T | A | 1 | a0003 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.895T>A | p.Ser299Thr | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/6 | 1232/11936 | 895/1437 | 299/478 | chr12 | 59775190 | ||
| chr12:59775191
|
C | T | 1 | a0003 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.896C>T | p.Ser299Phe | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/6 | 1233/11936 | 896/1437 | 299/478 | chr12 | 59775191 | ||
| chr12:59775331
|
T | G | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1036T>G | p.Phe346Val | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/6 | 1373/11936 | 1036/1437 | 346/478 | chr12 | 59775331 | ||
| chr12:59779498
|
T | C | 1 | a0005 | 1 | NA19075.hp2 | missense_variant | MODERATE | c.1256T>C | p.Val419Ala | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1593/11936 | 1256/1437 | 419/478 | chr12 | 59779498 | ||
| chr12:59779575
|
A | T | 3 | a0002a0005a0008 | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
missense_variant | MODERATE | c.1333A>T | p.Thr445Ser | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1670/11936 | 1333/1437 | 445/478 | chr12 | 59779575 | ||
| chr12:59779673
|
C | G | 1 | a0006 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1431C>G | p.Asn477Lys | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1768/11936 | 1431/1437 | 477/478 | chr12 | 59779673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:59704906
|
A | G | 1 | a0004c0005 | 2 | HG02976.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.105A>G | p.Ala35Ala | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/6 | 442/11936 | 105/1437 | 35/478 | chr12 | 59704906 | ||
| chr12:59705002
|
T | G | 1 | a0002c0006 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.201T>G | p.Ala67Ala | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/6 | 538/11936 | 201/1437 | 67/478 | chr12 | 59705002 | ||
| chr12:59779625
|
C | T | 1 | a0001c0003 | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
synonymous_variant | LOW | c.1383C>T | p.Asn461Asn | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1720/11936 | 1383/1437 | 461/478 | chr12 | 59779625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:59704788
|
C | T | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/6 | 14 | chr12 | 59704788 | |||||
| chr12:59779844
|
AACTT | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*171_*174delCTTA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 171 | INFO_REALIGN_3_PRIME | chr12 | 59779844 | ||||
| chr12:59779945
|
C | CTAAT | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*268_*271dupAATT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 272 | INFO_REALIGN_3_PRIME | chr12 | 59779945 | ||||
| chr12:59780025
|
A | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*346A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 346 | chr12 | 59780025 | |||||
| chr12:59780097
|
A | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*418A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 418 | chr12 | 59780097 | |||||
| chr12:59780107
|
G | A | 1 | a0001c0003t0005 | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*428G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 428 | chr12 | 59780107 | |||||
| chr12:59780162
|
C | G | 1 | a0001c0001t0044 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 483 | chr12 | 59780162 | |||||
| chr12:59780415
|
A | C | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 736 | chr12 | 59780415 | |||||
| chr12:59780712
|
G | A | 10 | a0002c0002t0003a0002c0002t0004a0002c0002t0008others(7): Show | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1033G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1033 | chr12 | 59780712 | |||||
| chr12:59780734
|
A | G | 1 | a0001c0001t0043 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1055 | chr12 | 59780734 | |||||
| chr12:59780831
|
C | T | 1 | a0001c0001t0042 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1152C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1152 | chr12 | 59780831 | |||||
| chr12:59781222
|
A | G | 1 | a0002c0002t0024 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1543A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1543 | chr12 | 59781222 | |||||
| chr12:59781284
|
C | CATT | 14 | a0001c0001t0006a0001c0001t0012a0001c0001t0015others(11): Show | 50 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1607_*1608insTAT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 1608 | INFO_REALIGN_3_PRIME | chr12 | 59781284 | ||||
| chr12:59781721
|
G | T | 1 | a0001c0001t0041 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2042 | chr12 | 59781721 | |||||
| chr12:59781785
|
C | A | 6 | a0001c0001t0009a0001c0001t0013a0001c0001t0025others(3): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2106C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2106 | chr12 | 59781785 | |||||
| chr12:59781787
|
A | G | 1 | a0001c0001t0039 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2108A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2108 | chr12 | 59781787 | |||||
| chr12:59781824
|
C | T | 7 | a0002c0002t0003a0002c0002t0004a0002c0002t0016others(4): Show | 63 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2145C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2145 | chr12 | 59781824 | |||||
| chr12:59781905
|
A | ATT | 1 | a0001c0003t0005 | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2227_*2228dupTT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2229 | INFO_REALIGN_3_PRIME | chr12 | 59781905 | ||||
| chr12:59782006
|
T | C | 1 | a0001c0001t0015 | 2 | HG02559.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2327T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2327 | chr12 | 59782006 | |||||
| chr12:59782008
|
G | A | 8 | a0001c0001t0012a0001c0001t0018a0001c0001t0019others(5): Show | 13 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2329G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2329 | chr12 | 59782008 | |||||
| chr12:59782233
|
A | G | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2554A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2554 | chr12 | 59782233 | |||||
| chr12:59782306
|
C | G | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2627C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2627 | chr12 | 59782306 | |||||
| chr12:59782400
|
T | C | 2 | a0001c0001t0045a0001c0001t0046 | 2 | HG02559.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2721T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2721 | chr12 | 59782400 | |||||
| chr12:59782568
|
A | T | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2889A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2889 | chr12 | 59782568 | |||||
| chr12:59782645
|
G | A | 1 | a0001c0001t0026 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 2966 | chr12 | 59782645 | |||||
| chr12:59782693
|
C | T | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3014C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3014 | chr12 | 59782693 | |||||
| chr12:59782795
|
C | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3116C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3116 | chr12 | 59782795 | |||||
| chr12:59782798
|
A | C | 32 | a0001c0001t0006a0001c0001t0009a0001c0001t0012others(29): Show | 134 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*3119A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3119 | chr12 | 59782798 | |||||
| chr12:59782968
|
T | C | 1 | a0001c0001t0027 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3289T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3289 | chr12 | 59782968 | |||||
| chr12:59783004
|
A | G | 1 | a0002c0006t0022 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3325A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3325 | chr12 | 59783004 | |||||
| chr12:59783137
|
A | T | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3458A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3458 | chr12 | 59783137 | |||||
| chr12:59783141
|
A | AT | 2 | a0001c0001t0011a0001c0001t0027 | 5 | HG02071.hp1 NA18747.hp1 NA18951.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3468dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3469 | INFO_REALIGN_3_PRIME | chr12 | 59783141 | ||||
| chr12:59783224
|
T | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3545T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3545 | chr12 | 59783224 | |||||
| chr12:59783225
|
AG | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3548delG | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3548 | INFO_REALIGN_3_PRIME | chr12 | 59783225 | ||||
| chr12:59783499
|
G | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03239.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3820G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3820 | chr12 | 59783499 | |||||
| chr12:59783506
|
A | G | 1 | a0001c0001t0035 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3827A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3827 | chr12 | 59783506 | |||||
| chr12:59783637
|
A | ATTTCTTT others(1): Show |
5 | a0001c0001t0006a0001c0001t0015a0001c0001t0021others(2): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3970_*3977dupCTTT others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3978 | INFO_REALIGN_3_PRIME | chr12 | 59783637 | ||||
| chr12:59783637
|
A | ATTTCTTT others(5): Show |
5 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(2): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3966_*3977dupCTTT others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3978 | INFO_REALIGN_3_PRIME | chr12 | 59783637 | ||||
| chr12:59783653
|
C | CTTTCTTT others(6): Show |
1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3977_*3978insCTTT others(9): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 3978 | INFO_REALIGN_3_PRIME | chr12 | 59783653 | ||||
| chr12:59783702
|
C | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4023C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4023 | chr12 | 59783702 | |||||
| chr12:59783713
|
A | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4034A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4034 | chr12 | 59783713 | |||||
| chr12:59783718
|
C | T | 1 | a0001c0001t0037 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4039C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4039 | chr12 | 59783718 | |||||
| chr12:59783720
|
C | T | 1 | a0001c0001t0041 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4041C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4041 | chr12 | 59783720 | |||||
| chr12:59783756
|
A | G | 9 | a0001c0001t0038a0002c0002t0003a0002c0002t0004others(6): Show | 65 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*4077A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4077 | chr12 | 59783756 | |||||
| chr12:59783760
|
T | A | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4081T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4081 | chr12 | 59783760 | |||||
| chr12:59784276
|
C | T | 2 | a0001c0001t0014a0001c0003t0005 | 21 | HG00621.hp1 HG00673.hp2 HG01261.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4597C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4597 | chr12 | 59784276 | |||||
| chr12:59784376
|
A | T | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4697A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4697 | chr12 | 59784376 | |||||
| chr12:59784453
|
G | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4774G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4774 | chr12 | 59784453 | |||||
| chr12:59784629
|
T | G | 4 | a0001c0001t0006a0001c0001t0015a0001c0001t0021others(1): Show | 19 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4950T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 4950 | chr12 | 59784629 | |||||
| chr12:59784808
|
G | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5129G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5129 | chr12 | 59784808 | |||||
| chr12:59785020
|
A | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5341A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5341 | chr12 | 59785020 | |||||
| chr12:59785129
|
G | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5450G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5450 | chr12 | 59785129 | |||||
| chr12:59785159
|
C | T | 15 | a0001c0001t0006a0001c0001t0012a0001c0001t0014others(12): Show | 53 | HG00621.hp1 HG00673.hp2 HG01109.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5480C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5480 | chr12 | 59785159 | |||||
| chr12:59785190
|
A | C | 1 | a0001c0001t0034 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5511A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5511 | chr12 | 59785190 | |||||
| chr12:59785289
|
C | T | 1 | a0001c0001t0033 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5610C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5610 | chr12 | 59785289 | |||||
| chr12:59785396
|
T | A | 3 | a0001c0001t0038a0002c0002t0004a0002c0002t0023 | 25 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5717T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5717 | chr12 | 59785396 | |||||
| chr12:59785467
|
G | A | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5788G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 5788 | chr12 | 59785467 | |||||
| chr12:59785808
|
T | G | 7 | a0001c0001t0009a0001c0001t0013a0001c0001t0025others(4): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6129T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6129 | chr12 | 59785808 | |||||
| chr12:59785891
|
T | C | 1 | a0001c0001t0028 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6212T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6212 | chr12 | 59785891 | |||||
| chr12:59785926
|
A | G | 1 | a0001c0001t0046 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6247A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6247 | chr12 | 59785926 | |||||
| chr12:59785935
|
A | G | 1 | a0002c0002t0017 | 2 | HG00609.hp1 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6256A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6256 | chr12 | 59785935 | |||||
| chr12:59785987
|
A | C | 1 | a0001c0001t0045 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6308A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6308 | chr12 | 59785987 | |||||
| chr12:59786033
|
G | T | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6354G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6354 | chr12 | 59786033 | |||||
| chr12:59786041
|
C | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6362C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6362 | chr12 | 59786041 | |||||
| chr12:59786041
|
C | T | 5 | a0001c0001t0010a0001c0001t0031a0001c0001t0032others(2): Show | 7 | HG00639.hp2 HG01123.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6362C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6362 | chr12 | 59786041 | |||||
| chr12:59786048
|
G | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6369G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6369 | chr12 | 59786048 | |||||
| chr12:59786049
|
G | C | 1 | a0002c0002t0016 | 2 | NA18973.hp2 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6370G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6370 | chr12 | 59786049 | |||||
| chr12:59786050
|
G | C | 1 | a0001c0001t0012 | 4 | HG02257.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6371G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6371 | chr12 | 59786050 | |||||
| chr12:59786066
|
G | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6387G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6387 | chr12 | 59786066 | |||||
| chr12:59786072
|
T | C | 1 | a0001c0001t0031 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6393T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6393 | chr12 | 59786072 | |||||
| chr12:59786094
|
G | A | 1 | a0001c0001t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6415G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6415 | chr12 | 59786094 | |||||
| chr12:59786191
|
T | TAAATAAA others(3): Show |
4 | a0001c0001t0020a0001c0001t0045a0001c0001t0046others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6524_*6533dupAATA others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6534 | INFO_REALIGN_3_PRIME | chr12 | 59786191 | ||||
| chr12:59786191
|
T | TAAATAAA others(8): Show |
2 | a0001c0001t0012a0001c0001t0019 | 6 | HG02257.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6519_*6533dupAATA others(11): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6534 | INFO_REALIGN_3_PRIME | chr12 | 59786191 | ||||
| chr12:59786346
|
AT | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6668delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 6668 | chr12 | 59786346 | |||||
| chr12:59786700
|
A | C | 1 | a0001c0001t0014 | 3 | HG00673.hp2 HG02155.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7021A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7021 | chr12 | 59786700 | |||||
| chr12:59786990
|
G | A | 1 | a0001c0001t0029 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7311G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7311 | chr12 | 59786990 | |||||
| chr12:59787002
|
G | A | 1 | a0007c0008t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7323G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7323 | chr12 | 59787002 | |||||
| chr12:59787004
|
G | C | 1 | a0007c0008t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7325G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7325 | chr12 | 59787004 | |||||
| chr12:59787061
|
T | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7382T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7382 | chr12 | 59787061 | |||||
| chr12:59787090
|
ATATTG | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7416_*7420delGTAT others(1): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7416 | INFO_REALIGN_3_PRIME | chr12 | 59787090 | ||||
| chr12:59787102
|
T | C | 5 | a0001c0001t0009a0001c0001t0025a0001c0001t0042others(2): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7423T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7423 | chr12 | 59787102 | |||||
| chr12:59787167
|
G | A | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*7488G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7488 | chr12 | 59787167 | |||||
| chr12:59787183
|
G | A | 48 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(45): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*7504G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7504 | chr12 | 59787183 | |||||
| chr12:59787499
|
A | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7820A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7820 | chr12 | 59787499 | |||||
| chr12:59787556
|
T | A | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7877T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 7877 | chr12 | 59787556 | |||||
| chr12:59787970
|
T | C | 1 | a0002c0002t0023 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8291T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 8291 | chr12 | 59787970 | |||||
| chr12:59788100
|
A | AT | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8423dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 8424 | INFO_REALIGN_3_PRIME | chr12 | 59788100 | ||||
| chr12:59788463
|
T | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8784T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 8784 | chr12 | 59788463 | |||||
| chr12:59788591
|
TA | T | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8916delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 8916 | INFO_REALIGN_3_PRIME | chr12 | 59788591 | ||||
| chr12:59788643
|
T | C | 10 | a0001c0001t0007a0001c0001t0010a0001c0001t0029others(7): Show | 25 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*8964T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 8964 | chr12 | 59788643 | |||||
| chr12:59788712
|
T | A | 1 | a0001c0001t0032 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9033T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9033 | chr12 | 59788712 | |||||
| chr12:59788900
|
A | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9221A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9221 | chr12 | 59788900 | |||||
| chr12:59788950
|
A | C | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*9271A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9271 | chr12 | 59788950 | |||||
| chr12:59788952
|
C | T | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0021 | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*9273C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9273 | chr12 | 59788952 | |||||
| chr12:59788973
|
T | A | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9294T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9294 | chr12 | 59788973 | |||||
| chr12:59788984
|
T | C | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9305T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9305 | chr12 | 59788984 | |||||
| chr12:59789125
|
A | G | 7 | a0001c0001t0012a0001c0001t0019a0001c0001t0020others(4): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9446A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9446 | chr12 | 59789125 | |||||
| chr12:59789424
|
G | A | 2 | a0001c0001t0014a0001c0003t0005 | 21 | HG00621.hp1 HG00673.hp2 HG01261.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9745G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9745 | chr12 | 59789424 | |||||
| chr12:59789562
|
C | G | 1 | a0001c0001t0025 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9883C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 9883 | chr12 | 59789562 | |||||
| chr12:59789837
|
T | C | 1 | a0001c0001t0041 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10158T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 6/6 | 10158 | chr12 | 59789837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:59596288
|
C | G | 7 | a0001c0001t0001g0260a0001c0001t0006g0255a0001c0001t0012g0254others(4): Show | 7 | HG01175.hp1 HG01257.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-130+52C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596288 | ||||||
| chr12:59596489
|
TGA | T | 184 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0113others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-130+255_-130+256d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59596489 | |||||
| chr12:59596515
|
A | AG | 188 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0113others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-130+281dupG | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59596515 | |||||
| chr12:59596569
|
C | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-130+333C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596569 | ||||||
| chr12:59596728
|
G | T | 1 | a0001c0001t0002g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-130+492G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596728 | ||||||
| chr12:59596822
|
G | T | 27 | a0001c0001t0001g0260a0001c0001t0006g0253a0001c0001t0006g0255others(24): Show | 27 | HG00099.hp1 HG01123.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-130+586G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596822 | ||||||
| chr12:59596967
|
G | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-130+731G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596967 | ||||||
| chr12:59596986
|
T | C | 8 | a0001c0001t0010g0237a0001c0001t0032g0234a0001c0001t0036g0241others(5): Show | 8 | HG00099.hp1 HG01123.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.-130+750T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59596986 | ||||||
| chr12:59597222
|
T | TAC | 13 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-130+1033_-130+103 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
T | TACAC | 13 | a0001c0001t0001g0003a0001c0001t0002g0055a0001c0001t0002g0082others(10): Show | 13 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-130+1031_-130+103 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
T | TACACAC | 10 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0006g0001others(7): Show | 10 | HG01496.hp1 HG01891.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-130+1029_-130+103 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0079a0001c0001t0019g0242 | 3 | HG02896.hp1 NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-130+1027_-130+103 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
T | TACACACA others(3): Show |
2 | a0002c0002t0008g0072a0002c0006t0022g0078 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-130+1025_-130+103 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TAC | T | 46 | a0001c0001t0001g0067a0001c0001t0001g0113a0001c0001t0001g0121others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-130+1033_-130+103 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TACAC | T | 68 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0163others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-130+1031_-130+103 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TACACAC | T | 47 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 47 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-130+1029_-130+103 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TACACACA others(1): Show |
T | 25 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0041others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-130+1027_-130+103 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0041g0232others(1): Show | 4 | HG02630.hp2 NA18954.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+1025_-130+103 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597222
|
TACACACA others(5): Show |
T | 2 | a0002c0002t0003g0076a0004c0005t0009g0233 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-130+1023_-130+103 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59597222 | |||||
| chr12:59597366
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-130+1130C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597366 | ||||||
| chr12:59597474
|
C | G | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-130+1238C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597474 | ||||||
| chr12:59597506
|
G | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 46 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-130+1270G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597506 | ||||||
| chr12:59597507
|
A | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 46 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-130+1271A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597507 | ||||||
| chr12:59597696
|
A | G | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+1460A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597696 | ||||||
| chr12:59597711
|
G | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-130+1475G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597711 | ||||||
| chr12:59597874
|
C | T | 76 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0124others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-130+1638C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59597874 | ||||||
| chr12:59598230
|
T | C | 182 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0113others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-130+1994T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598230 | ||||||
| chr12:59598258
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0006g0001 | 2 | HG00738.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-130+2022T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598258 | ||||||
| chr12:59598282
|
G | A | 1 | a0001c0001t0006g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-130+2046G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598282 | ||||||
| chr12:59598420
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2184C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598420 | ||||||
| chr12:59598474
|
ATTTGCCT others(5): Show |
A | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-130+2240_-130+225 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59598474 | |||||
| chr12:59598487
|
T | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2251T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598487 | ||||||
| chr12:59598490
|
A | AT | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2262dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59598490 | |||||
| chr12:59598508
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2272A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598508 | ||||||
| chr12:59598510
|
G | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-130+2274G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598510 | ||||||
| chr12:59598621
|
A | G | 76 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0124others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-130+2385A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598621 | ||||||
| chr12:59598640
|
C | T | 1 | a0002c0002t0004g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-130+2404C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598640 | ||||||
| chr12:59598677
|
G | A | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+2441G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598677 | ||||||
| chr12:59598710
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-130+2474G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59598710 | ||||||
| chr12:59599044
|
C | T | 180 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0113others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-130+2808C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599044 | ||||||
| chr12:59599063
|
C | T | 76 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0124others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-130+2827C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599063 | ||||||
| chr12:59599093
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2857A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599093 | ||||||
| chr12:59599097
|
TA | T | 180 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0113others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-130+2864delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59599097 | |||||
| chr12:59599163
|
G | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-130+2927G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599163 | ||||||
| chr12:59599399
|
G | A | 2 | a0002c0002t0003g0076a0002c0002t0008g0072 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-130+3163G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599399 | ||||||
| chr12:59599792
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-130+3556C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599792 | ||||||
| chr12:59599831
|
G | A | 1 | a0001c0001t0036g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-130+3595G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599831 | ||||||
| chr12:59599835
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-130+3599G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599835 | ||||||
| chr12:59599938
|
T | G | 3 | a0001c0001t0048g0081a0002c0002t0003g0076a0002c0002t0008g0072 | 3 | HG02145.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-130+3702T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599938 | ||||||
| chr12:59599963
|
G | A | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+3727G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59599963 | ||||||
| chr12:59600029
|
C | A | 1 | a0001c0003t0005g0007 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-130+3793C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600029 | ||||||
| chr12:59600101
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-130+3865A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600101 | ||||||
| chr12:59600227
|
T | G | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-130+3991T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600227 | ||||||
| chr12:59600236
|
T | A | 1 | a0002c0002t0017g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-130+4000T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600236 | ||||||
| chr12:59600462
|
CT | C | 5 | a0001c0001t0001g0175a0001c0001t0048g0081a0002c0002t0003g0076others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-130+4240delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59600462 | |||||
| chr12:59600573
|
T | A | 1 | a0002c0002t0003g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-130+4337T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600573 | ||||||
| chr12:59600935
|
C | T | 3 | a0001c0001t0048g0081a0002c0002t0003g0076a0002c0002t0008g0072 | 3 | HG02145.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-130+4699C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600935 | ||||||
| chr12:59600988
|
A | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-130+4752A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59600988 | ||||||
| chr12:59601305
|
A | T | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+5069A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59601305 | ||||||
| chr12:59601378
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-130+5142T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59601378 | ||||||
| chr12:59601629
|
C | T | 9 | a0001c0001t0002g0118a0001c0001t0006g0117a0001c0001t0006g0171others(6): Show | 9 | HG01496.hp2 HG02109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-130+5393C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59601629 | ||||||
| chr12:59601976
|
A | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+5740A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59601976 | ||||||
| chr12:59602012
|
C | T | 3 | a0001c0001t0013g0073a0001c0003t0005g0074a0001c0003t0005g0075 | 3 | HG01884.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-130+5776C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602012 | ||||||
| chr12:59602218
|
T | A | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-130+5982T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602218 | ||||||
| chr12:59602399
|
G | A | 2 | a0001c0001t0048g0081a0002c0002t0003g0229 | 2 | HG02145.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-130+6163G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602399 | ||||||
| chr12:59602412
|
T | C | 3 | a0001c0001t0009g0243a0003c0004t0009g0249a0003c0004t0009g0250 | 3 | HG01167.hp2 HG01169.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-130+6176T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602412 | ||||||
| chr12:59602479
|
C | CT | 128 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-130+6265dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59602479 | |||||
| chr12:59602479
|
C | CTT | 28 | a0001c0001t0006g0225a0001c0001t0006g0253a0001c0001t0009g0244others(25): Show | 28 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-130+6264_-130+626 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59602479 | |||||
| chr12:59602557
|
C | T | 3 | a0001c0001t0020g0006a0002c0002t0003g0085a0002c0002t0008g0088 | 3 | HG02145.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-130+6321C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602557 | ||||||
| chr12:59602628
|
C | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+6392C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602628 | ||||||
| chr12:59602640
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-130+6404C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602640 | ||||||
| chr12:59602674
|
A | G | 10 | a0001c0001t0007g0168a0001c0001t0046g0002a0002c0002t0003g0076others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-130+6438A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602674 | ||||||
| chr12:59602676
|
G | C | 23 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0124others(20): Show | 23 | HG00408.hp2 HG00597.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-130+6440G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602676 | ||||||
| chr12:59602677
|
G | C | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+6441G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602677 | ||||||
| chr12:59602715
|
C | G | 1 | a0002c0002t0003g0100 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-130+6479C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602715 | ||||||
| chr12:59602723
|
G | A | 1 | a0002c0002t0004g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-130+6487G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602723 | ||||||
| chr12:59602761
|
A | C | 11 | a0001c0001t0001g0041a0001c0001t0001g0143a0001c0001t0001g0215others(8): Show | 11 | HG00140.hp2 HG02071.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-130+6525A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602761 | ||||||
| chr12:59602859
|
G | A | 1 | a0001c0001t0010g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-130+6623G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59602859 | ||||||
| chr12:59603072
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-130+6836A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603072 | ||||||
| chr12:59603125
|
A | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-130+6889A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603125 | ||||||
| chr12:59603326
|
T | C | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-130+7090T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603326 | ||||||
| chr12:59603482
|
C | G | 3 | a0001c0001t0006g0253a0001c0001t0048g0081a0002c0002t0008g0251 | 3 | HG02145.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-130+7246C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603482 | ||||||
| chr12:59603623
|
A | C | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-130+7387A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603623 | ||||||
| chr12:59603880
|
T | C | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+7644T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603880 | ||||||
| chr12:59603961
|
A | C | 19 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(16): Show | 19 | HG00597.hp2 HG01261.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-130+7725A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603961 | ||||||
| chr12:59603978
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-130+7742A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59603978 | ||||||
| chr12:59604131
|
T | C | 2 | a0001c0001t0002g0146a0002c0002t0003g0147 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-130+7895T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59604131 | ||||||
| chr12:59604653
|
T | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(106): Show | 109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-130+8417T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59604653 | ||||||
| chr12:59604656
|
G | A | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-130+8420G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59604656 | ||||||
| chr12:59604982
|
G | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-130+8746G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59604982 | ||||||
| chr12:59605009
|
G | A | 13 | a0001c0001t0002g0148a0001c0001t0002g0197a0001c0001t0010g0123others(10): Show | 13 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-130+8773G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605009 | ||||||
| chr12:59605030
|
C | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+8794C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605030 | ||||||
| chr12:59605280
|
A | C | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-130+9044A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605280 | ||||||
| chr12:59605404
|
A | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+9168A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605404 | ||||||
| chr12:59605487
|
T | C | 1 | a0001c0001t0006g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-130+9251T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605487 | ||||||
| chr12:59605550
|
A | T | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-130+9314A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605550 | ||||||
| chr12:59605605
|
A | T | 5 | a0001c0001t0006g0253a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+9369A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59605605 | ||||||
| chr12:59606072
|
C | A | 16 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-130+9836C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606072 | ||||||
| chr12:59606217
|
C | T | 1 | a0002c0002t0004g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-130+9981C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606217 | ||||||
| chr12:59606378
|
G | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+10142G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606378 | ||||||
| chr12:59606533
|
G | A | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-130+10297G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606533 | ||||||
| chr12:59606633
|
G | A | 32 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(29): Show | 32 | HG00597.hp2 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.-130+10397G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606633 | ||||||
| chr12:59606672
|
C | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+10436C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606672 | ||||||
| chr12:59606685
|
C | T | 11 | a0001c0001t0002g0051a0001c0001t0002g0193a0001c0001t0002g0210others(8): Show | 11 | HG00423.hp2 HG02040.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.-130+10449C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606685 | ||||||
| chr12:59606712
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-130+10476A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606712 | ||||||
| chr12:59606839
|
T | A | 1 | a0001c0001t0007g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-130+10603T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606839 | ||||||
| chr12:59606860
|
A | ATG | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-130+10635_-130+10 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59606860 | |||||
| chr12:59606860
|
ATG | A | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+10635_-130+10 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59606860 | |||||
| chr12:59606947
|
A | T | 7 | a0001c0001t0001g0104a0001c0001t0001g0129a0001c0001t0001g0176others(4): Show | 7 | HG02165.hp2 NA18977.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-130+10711A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59606947 | ||||||
| chr12:59607080
|
C | T | 1 | a0001c0003t0005g0007 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-130+10844C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607080 | ||||||
| chr12:59607145
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+10909C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607145 | ||||||
| chr12:59607156
|
GA | G | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0019g0242others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+10930delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59607156 | |||||
| chr12:59607215
|
G | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+10979G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607215 | ||||||
| chr12:59607232
|
A | T | 1 | a0001c0003t0005g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-130+10996A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607232 | ||||||
| chr12:59607449
|
G | A | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+11213G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607449 | ||||||
| chr12:59607588
|
CTG | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0118a0001c0001t0013g0069 | 3 | HG02109.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-130+11353_-130+11 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607588 | ||||||
| chr12:59607957
|
A | C | 17 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(14): Show | 17 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-130+11721A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59607957 | ||||||
| chr12:59608074
|
C | A | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+11838C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608074 | ||||||
| chr12:59608503
|
A | G | 17 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(14): Show | 17 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-130+12267A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608503 | ||||||
| chr12:59608528
|
C | G | 1 | a0001c0001t0011g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-130+12292C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608528 | ||||||
| chr12:59608876
|
G | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+12640G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608876 | ||||||
| chr12:59608909
|
C | T | 5 | a0001c0001t0006g0253a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+12673C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608909 | ||||||
| chr12:59608952
|
A | C | 12 | a0001c0001t0006g0117a0001c0001t0006g0159a0001c0001t0006g0167others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-130+12716A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59608952 | ||||||
| chr12:59609144
|
G | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+12908G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609144 | ||||||
| chr12:59609322
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+13086G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609322 | ||||||
| chr12:59609358
|
G | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+13122G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609358 | ||||||
| chr12:59609448
|
G | C | 6 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(3): Show | 6 | HG01175.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-130+13212G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609448 | ||||||
| chr12:59609459
|
C | A | 1 | a0001c0001t0006g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-130+13223C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609459 | ||||||
| chr12:59609506
|
G | A | 8 | a0001c0001t0009g0243a0001c0001t0025g0248a0001c0001t0043g0047others(5): Show | 8 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-130+13270G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609506 | ||||||
| chr12:59609805
|
A | G | 1 | a0001c0003t0005g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-130+13569A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609805 | ||||||
| chr12:59609917
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+13681G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609917 | ||||||
| chr12:59609933
|
C | T | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+13697C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609933 | ||||||
| chr12:59609999
|
T | C | 1 | a0001c0003t0005g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-130+13763T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59609999 | ||||||
| chr12:59610019
|
A | C | 2 | a0001c0003t0005g0093a0001c0003t0005g0116 | 2 | HG03490.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-130+13783A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610019 | ||||||
| chr12:59610092
|
T | G | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-130+13856T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610092 | ||||||
| chr12:59610151
|
A | G | 6 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(3): Show | 6 | HG01175.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-130+13915A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610151 | ||||||
| chr12:59610168
|
G | A | 1 | a0002c0002t0008g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-130+13932G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610168 | ||||||
| chr12:59610277
|
A | C | 23 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(20): Show | 23 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-130+14041A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610277 | ||||||
| chr12:59610309
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+14073G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610309 | ||||||
| chr12:59610396
|
T | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+14160T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610396 | ||||||
| chr12:59610454
|
A | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+14218A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610454 | ||||||
| chr12:59610627
|
G | C | 1 | a0002c0002t0003g0191 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-130+14391G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610627 | ||||||
| chr12:59610800
|
T | C | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+14564T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610800 | ||||||
| chr12:59610831
|
A | C | 1 | a0001c0003t0005g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-130+14595A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610831 | ||||||
| chr12:59610868
|
G | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+14632G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59610868 | ||||||
| chr12:59610960
|
CAAGATCA | C | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+14726_-130+14 others(13): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59610960 | |||||
| chr12:59611000
|
C | T | 17 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(14): Show | 17 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-130+14764C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611000 | ||||||
| chr12:59611018
|
G | T | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-130+14782G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611018 | ||||||
| chr12:59611037
|
C | T | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-130+14801C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611037 | ||||||
| chr12:59611327
|
G | A | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-130+15091G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611327 | ||||||
| chr12:59611379
|
A | G | 5 | a0001c0001t0006g0253a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+15143A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611379 | ||||||
| chr12:59611382
|
A | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+15146A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611382 | ||||||
| chr12:59611638
|
C | T | 22 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-130+15402C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611638 | ||||||
| chr12:59611647
|
C | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+15411C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611647 | ||||||
| chr12:59611686
|
AGCAAGTT others(89): Show |
A | 1 | a0001c0001t0002g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-130+15457_-130+15 others(102): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59611686 | |||||
| chr12:59611713
|
A | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+15477A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611713 | ||||||
| chr12:59611799
|
A | G | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+15563A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611799 | ||||||
| chr12:59611945
|
A | G | 23 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(20): Show | 23 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-130+15709A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59611945 | ||||||
| chr12:59612152
|
G | A | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+15916G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612152 | ||||||
| chr12:59612180
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(105): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-130+15944C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612180 | ||||||
| chr12:59612283
|
C | T | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-130+16047C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612283 | ||||||
| chr12:59612418
|
G | C | 2 | a0002c0002t0003g0008a0002c0002t0003g0228 | 2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-130+16182G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612418 | ||||||
| chr12:59612524
|
G | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-130+16288G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612524 | ||||||
| chr12:59612588
|
G | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-130+16352G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612588 | ||||||
| chr12:59612612
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-130+16376A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612612 | ||||||
| chr12:59612623
|
C | T | 4 | a0002c0002t0003g0085a0002c0002t0003g0169a0002c0002t0003g0170others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130+16387C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612623 | ||||||
| chr12:59612652
|
C | T | 1 | a0001c0001t0011g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-130+16416C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612652 | ||||||
| chr12:59612658
|
C | T | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-130+16422C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612658 | ||||||
| chr12:59612887
|
A | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+16651A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59612887 | ||||||
| chr12:59613015
|
C | G | 1 | a0001c0001t0002g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-130+16779C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613015 | ||||||
| chr12:59613017
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-130+16781G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613017 | ||||||
| chr12:59613034
|
C | T | 1 | a0002c0002t0004g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-130+16798C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613034 | ||||||
| chr12:59613060
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-130+16824G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613060 | ||||||
| chr12:59613147
|
G | A | 5 | a0001c0001t0002g0146a0002c0002t0003g0060a0002c0002t0003g0147others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-130+16911G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613147 | ||||||
| chr12:59613260
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-130+17024T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613260 | ||||||
| chr12:59613315
|
G | A | 2 | a0001c0003t0005g0235a0001c0003t0005g0236 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-130+17079G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613315 | ||||||
| chr12:59613400
|
A | G | 1 | a0001c0001t0007g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-130+17164A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613400 | ||||||
| chr12:59613966
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-130+17730C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59613966 | ||||||
| chr12:59614007
|
G | C | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130+17771G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614007 | ||||||
| chr12:59614054
|
C | CT | 73 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 73 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-130+17834dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614054 | |||||
| chr12:59614054
|
CT | C | 13 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0009g0243others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-130+17834delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614054 | |||||
| chr12:59614072
|
A | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-130+17836A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614072 | ||||||
| chr12:59614176
|
G | C | 1 | a0002c0002t0004g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-130+17940G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614176 | ||||||
| chr12:59614178
|
G | A | 2 | a0002c0002t0004g0056a0002c0002t0004g0098 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-130+17942G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614178 | ||||||
| chr12:59614192
|
A | C | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-130+17956A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614192 | ||||||
| chr12:59614301
|
T | A | 1 | a0001c0001t0034g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-130+18065T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614301 | ||||||
| chr12:59614330
|
C | A | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-130+18094C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614330 | ||||||
| chr12:59614707
|
G | T | 1 | a0002c0002t0003g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-130+18471G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614707 | ||||||
| chr12:59614734
|
C | T | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-130+18498C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614734 | ||||||
| chr12:59614754
|
C | T | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-130+18518C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59614754 | ||||||
| chr12:59614824
|
T | TA | 48 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0067others(45): Show | 48 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-130+18617dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614824 | |||||
| chr12:59614824
|
T | TAA | 91 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-130+18616_-130+18 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614824 | |||||
| chr12:59614824
|
T | TAAA | 12 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0104others(9): Show | 12 | HG00423.hp1 HG00423.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-130+18615_-130+18 others(9): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614824 | |||||
| chr12:59614824
|
TA | T | 8 | a0001c0001t0002g0065a0001c0001t0002g0112a0001c0001t0002g0132others(5): Show | 8 | HG00673.hp1 HG02080.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-130+18617delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59614824 | |||||
| chr12:59615091
|
T | C | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+18855T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615091 | ||||||
| chr12:59615282
|
CACAA | C | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+19050_-130+19 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59615282 | |||||
| chr12:59615322
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+19086C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615322 | ||||||
| chr12:59615369
|
C | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 16 | HG00438.hp1 HG00673.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-130+19133C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615369 | ||||||
| chr12:59615375
|
A | T | 3 | a0001c0001t0043g0047a0001c0001t0046g0002a0001c0001t0048g0081 | 3 | HG02145.hp2 HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-130+19139A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615375 | ||||||
| chr12:59615470
|
G | T | 2 | a0001c0001t0046g0002a0001c0001t0048g0081 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-130+19234G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615470 | ||||||
| chr12:59615506
|
A | G | 1 | a0001c0001t0036g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-130+19270A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615506 | ||||||
| chr12:59615620
|
A | G | 1 | a0002c0002t0004g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-130+19384A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615620 | ||||||
| chr12:59615673
|
C | A | 4 | a0001c0001t0007g0130a0001c0001t0007g0139a0002c0002t0004g0056others(1): Show | 4 | HG02040.hp2 NA18942.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+19437C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615673 | ||||||
| chr12:59615808
|
G | A | 1 | a0002c0002t0004g0136 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-130+19572G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615808 | ||||||
| chr12:59615888
|
A | G | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-130+19652A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615888 | ||||||
| chr12:59615964
|
G | A | 4 | a0002c0002t0003g0085a0002c0002t0003g0169a0002c0002t0003g0170others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130+19728G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615964 | ||||||
| chr12:59615973
|
C | G | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+19737C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59615973 | ||||||
| chr12:59616011
|
A | G | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-130+19775A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616011 | ||||||
| chr12:59616019
|
T | C | 1 | a0002c0002t0004g0098 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-130+19783T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616019 | ||||||
| chr12:59616111
|
T | C | 1 | a0001c0001t0010g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-130+19875T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616111 | ||||||
| chr12:59616302
|
A | C | 8 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-130+20066A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616302 | ||||||
| chr12:59616369
|
A | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0118others(1): Show | 4 | HG01257.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+20133A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616369 | ||||||
| chr12:59616439
|
C | T | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+20203C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616439 | ||||||
| chr12:59616440
|
T | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+20204T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616440 | ||||||
| chr12:59616611
|
C | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-130+20375C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616611 | ||||||
| chr12:59616663
|
T | C | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+20427T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616663 | ||||||
| chr12:59616722
|
T | C | 2 | a0002c0002t0003g0094a0002c0002t0003g0100 | 2 | NA18747.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-130+20486T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616722 | ||||||
| chr12:59616860
|
G | A | 6 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0200others(3): Show | 6 | HG00609.hp2 HG00621.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-130+20624G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59616860 | ||||||
| chr12:59617064
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-130+20828G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617064 | ||||||
| chr12:59617065
|
A | C | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-130+20829A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617065 | ||||||
| chr12:59617185
|
A | G | 5 | a0001c0001t0007g0097a0001c0001t0007g0158a0001c0001t0007g0168others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+20949A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617185 | ||||||
| chr12:59617276
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-130+21040T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617276 | ||||||
| chr12:59617574
|
A | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+21338A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617574 | ||||||
| chr12:59617629
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-130+21393A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59617629 | ||||||
| chr12:59618037
|
C | T | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-130+21801C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59618037 | ||||||
| chr12:59618314
|
A | C | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-130+22078A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59618314 | ||||||
| chr12:59618593
|
TC | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.-130+22358delC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59618593 | ||||||
| chr12:59619078
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-130+22842G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619078 | ||||||
| chr12:59619222
|
A | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-130+22986A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619222 | ||||||
| chr12:59619240
|
T | C | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+23004T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619240 | ||||||
| chr12:59619365
|
G | T | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-130+23129G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619365 | ||||||
| chr12:59619579
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-130+23343C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619579 | ||||||
| chr12:59619601
|
A | T | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-130+23365A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619601 | ||||||
| chr12:59619796
|
A | G | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-130+23560A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619796 | ||||||
| chr12:59619988
|
G | C | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-130+23752G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59619988 | ||||||
| chr12:59620106
|
C | A | 17 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(14): Show | 17 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-130+23870C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620106 | ||||||
| chr12:59620115
|
T | A | 1 | a0001c0001t0011g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-130+23879T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620115 | ||||||
| chr12:59620218
|
G | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+23982G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620218 | ||||||
| chr12:59620326
|
C | T | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+24090C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620326 | ||||||
| chr12:59620348
|
C | T | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130+24112C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620348 | ||||||
| chr12:59620377
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-130+24141G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620377 | ||||||
| chr12:59620381
|
T | G | 1 | a0001c0001t0006g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-130+24145T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620381 | ||||||
| chr12:59620410
|
A | T | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130+24174A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620410 | ||||||
| chr12:59620844
|
A | G | 3 | a0001c0001t0043g0047a0001c0001t0046g0002a0001c0001t0048g0081 | 3 | HG02145.hp2 HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-130+24608A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620844 | ||||||
| chr12:59620986
|
G | C | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-130+24750G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59620986 | ||||||
| chr12:59621164
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-130+24928A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621164 | ||||||
| chr12:59621324
|
A | G | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+25088A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621324 | ||||||
| chr12:59621485
|
T | A | 1 | a0002c0002t0023g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-130+25249T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621485 | ||||||
| chr12:59621486
|
T | A | 1 | a0002c0002t0023g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-130+25250T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621486 | ||||||
| chr12:59621502
|
G | T | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-130+25266G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621502 | ||||||
| chr12:59621530
|
C | T | 22 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-130+25294C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621530 | ||||||
| chr12:59621578
|
A | G | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+25342A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621578 | ||||||
| chr12:59621629
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-130+25393T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621629 | ||||||
| chr12:59621657
|
G | C | 1 | a0001c0003t0005g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-130+25421G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621657 | ||||||
| chr12:59621800
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+25564G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621800 | ||||||
| chr12:59621820
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-130+25584G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59621820 | ||||||
| chr12:59622308
|
A | G | 1 | a0002c0002t0004g0230 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-130+26072A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622308 | ||||||
| chr12:59622315
|
A | G | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-130+26079A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622315 | ||||||
| chr12:59622328
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-130+26092T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622328 | ||||||
| chr12:59622337
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-130+26101T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622337 | ||||||
| chr12:59622751
|
T | C | 5 | a0001c0001t0006g0253a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+26515T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622751 | ||||||
| chr12:59622839
|
G | A | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-130+26603G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622839 | ||||||
| chr12:59622863
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-130+26627G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622863 | ||||||
| chr12:59622915
|
T | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-130+26679T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59622915 | ||||||
| chr12:59623046
|
C | CTG | 8 | a0001c0001t0002g0118a0001c0001t0002g0148a0001c0001t0006g0117others(5): Show | 8 | HG00099.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-130+26856_-130+26 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTG | C | 25 | a0001c0001t0001g0067a0001c0001t0001g0260a0001c0001t0002g0011others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-130+26856_-130+26 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTG | C | 60 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-130+26854_-130+26 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTGTG | C | 15 | a0001c0001t0002g0055a0001c0001t0006g0221a0001c0001t0006g0222others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.-130+26852_-130+26 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0129a0001c0001t0002g0193a0002c0002t0003g0135others(6): Show | 9 | HG00423.hp2 HG00597.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-130+26850_-130+26 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTGTGT others(3): Show |
C | 82 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(79): Show | 82 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-130+26848_-130+26 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTGTGT others(5): Show |
C | 3 | a0001c0001t0001g0215a0001c0001t0006g0001a0001c0003t0005g0009 | 3 | HG00140.hp2 HG01891.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-130+26846_-130+26 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623046
|
CTGTGTGT others(19): Show |
C | 1 | a0001c0001t0002g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-130+26832_-130+26 others(32): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59623046 | |||||
| chr12:59623084
|
G | A | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-130+26848G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623084 | ||||||
| chr12:59623093
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-130+26857T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623093 | ||||||
| chr12:59623137
|
C | G | 12 | a0001c0001t0002g0148a0001c0001t0010g0123a0001c0001t0010g0237others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-130+26901C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623137 | ||||||
| chr12:59623290
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-130+27054C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623290 | ||||||
| chr12:59623400
|
T | A | 1 | a0001c0001t0006g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-130+27164T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623400 | ||||||
| chr12:59623434
|
A | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130+27198A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623434 | ||||||
| chr12:59623738
|
T | C | 1 | a0001c0003t0005g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-130+27502T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623738 | ||||||
| chr12:59623770
|
G | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-130+27534G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59623770 | ||||||
| chr12:59624352
|
T | C | 1 | a0001c0001t0032g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-130+28116T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59624352 | ||||||
| chr12:59624609
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-130+28373C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59624609 | ||||||
| chr12:59624670
|
G | A | 23 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(20): Show | 23 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-130+28434G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59624670 | ||||||
| chr12:59624738
|
T | G | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-130+28502T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59624738 | ||||||
| chr12:59624738
|
T | TTG | 16 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0148others(13): Show | 16 | HG00140.hp1 HG00558.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-130+28536_-130+28 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
T | TTGTG | 11 | a0001c0001t0009g0244a0001c0001t0012g0166a0001c0001t0012g0246others(8): Show | 11 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-130+28534_-130+28 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
T | TTGTGTG | 3 | a0001c0001t0006g0255a0001c0001t0013g0259a0002c0006t0022g0078 | 3 | HG01884.hp1 HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-130+28532_-130+28 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
T | TTGTGTGT others(1): Show |
2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-130+28530_-130+28 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
TTG | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-130+28536_-130+28 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
TTGTG | T | 9 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0007g0168others(6): Show | 9 | HG02109.hp2 HG02717.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-130+28534_-130+28 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
TTGTGTG | T | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-130+28532_-130+28 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59624738
|
TTGTGTGT others(5): Show |
T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-130+28526_-130+28 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59624738 | |||||
| chr12:59625016
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00639.hp1 HG00738.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-130+28780T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59625016 | ||||||
| chr12:59625100
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-130+28864T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59625100 | ||||||
| chr12:59625508
|
A | AT | 9 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(6): Show | 9 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-130+29276dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59625508 | |||||
| chr12:59625714
|
G | A | 2 | a0001c0001t0007g0103a0001c0001t0007g0128 | 2 | HG00735.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-129-29438G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59625714 | ||||||
| chr12:59625724
|
C | T | 2 | a0002c0002t0003g0107a0002c0002t0003g0183 | 2 | HG00423.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-129-29428C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59625724 | ||||||
| chr12:59625782
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-29370A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59625782 | ||||||
| chr12:59626055
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-29097C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626055 | ||||||
| chr12:59626227
|
T | C | 1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-129-28925T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626227 | ||||||
| chr12:59626239
|
GT | G | 42 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.-129-28906delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59626239 | |||||
| chr12:59626391
|
G | A | 4 | a0001c0001t0002g0057a0001c0001t0002g0131a0001c0001t0002g0179others(1): Show | 4 | NA18944.hp1 NA18977.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-28761G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626391 | ||||||
| chr12:59626482
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0007g0031 | 3 | HG01928.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-129-28670A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626482 | ||||||
| chr12:59626613
|
C | T | 2 | a0001c0003t0005g0195a0002c0002t0008g0257 | 2 | HG01175.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-129-28539C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626613 | ||||||
| chr12:59626634
|
T | A | 3 | a0001c0001t0007g0168a0004c0005t0009g0089a0004c0005t0009g0233 | 3 | HG02717.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-129-28518T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59626634 | ||||||
| chr12:59627339
|
G | C | 1 | a0001c0003t0005g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-129-27813G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627339 | ||||||
| chr12:59627355
|
T | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-129-27797T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627355 | ||||||
| chr12:59627403
|
C | T | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-27749C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627403 | ||||||
| chr12:59627491
|
T | C | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-129-27661T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627491 | ||||||
| chr12:59627502
|
T | C | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-27650T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627502 | ||||||
| chr12:59627570
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-129-27582G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627570 | ||||||
| chr12:59627669
|
G | A | 3 | a0001c0001t0002g0061a0001c0001t0007g0070a0001c0001t0044g0050 | 3 | HG00741.hp2 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-129-27483G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627669 | ||||||
| chr12:59627712
|
T | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-27440T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627712 | ||||||
| chr12:59627725
|
C | G | 16 | a0001c0001t0001g0113a0001c0001t0006g0171a0001c0001t0006g0226others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.-129-27427C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627725 | ||||||
| chr12:59627800
|
T | A | 1 | a0001c0001t0002g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-129-27352T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59627800 | ||||||
| chr12:59627895
|
AAT | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0129a0001c0001t0001g0176others(3): Show | 6 | HG02165.hp2 NA18977.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-129-27244_-129-27 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59627895 | |||||
| chr12:59628311
|
T | A | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-129-26841T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628311 | ||||||
| chr12:59628326
|
C | T | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-26826C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628326 | ||||||
| chr12:59628428
|
A | C | 1 | a0001c0001t0007g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-129-26724A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628428 | ||||||
| chr12:59628429
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-26723A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628429 | ||||||
| chr12:59628496
|
C | T | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-26656C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628496 | ||||||
| chr12:59628524
|
T | C | 1 | a0002c0002t0003g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-129-26628T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628524 | ||||||
| chr12:59628592
|
T | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-26560T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628592 | ||||||
| chr12:59628689
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0002g0057 | 2 | NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-129-26463C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628689 | ||||||
| chr12:59628722
|
C | A | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-26430C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628722 | ||||||
| chr12:59628845
|
T | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0175a0001c0001t0028g0133 | 3 | NA18969.hp1 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-129-26307T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628845 | ||||||
| chr12:59628864
|
T | C | 6 | a0001c0001t0013g0259a0001c0001t0015g0258a0002c0002t0003g0085others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129-26288T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628864 | ||||||
| chr12:59628970
|
G | A | 1 | a0002c0002t0003g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-129-26182G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59628970 | ||||||
| chr12:59629027
|
T | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-26125T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59629027 | ||||||
| chr12:59629059
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-129-26093C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59629059 | ||||||
| chr12:59629095
|
T | C | 1 | a0001c0001t0010g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-129-26057T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59629095 | ||||||
| chr12:59629324
|
C | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-25828C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59629324 | ||||||
| chr12:59629742
|
CT | C | 16 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-129-25401delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59629742 | |||||
| chr12:59629916
|
A | C | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-129-25236A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59629916 | ||||||
| chr12:59630094
|
C | T | 7 | a0001c0001t0006g0253a0001c0001t0013g0259a0001c0001t0015g0258others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-129-25058C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630094 | ||||||
| chr12:59630173
|
A | C | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-129-24979A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630173 | ||||||
| chr12:59630217
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-129-24935C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630217 | ||||||
| chr12:59630349
|
A | G | 1 | a0001c0001t0007g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-129-24803A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630349 | ||||||
| chr12:59630432
|
T | A | 7 | a0001c0001t0006g0117a0001c0001t0006g0159a0001c0001t0006g0167others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-129-24720T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630432 | ||||||
| chr12:59630546
|
G | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-24606G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630546 | ||||||
| chr12:59630586
|
T | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-24566T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630586 | ||||||
| chr12:59630628
|
G | T | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-24524G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630628 | ||||||
| chr12:59630647
|
C | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-129-24505C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59630647 | ||||||
| chr12:59631226
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-129-23926G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59631226 | ||||||
| chr12:59631494
|
C | A | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-129-23658C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59631494 | ||||||
| chr12:59631511
|
C | T | 4 | a0001c0001t0002g0065a0001c0001t0011g0178a0001c0001t0013g0069others(1): Show | 4 | HG00673.hp1 HG02886.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-23641C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59631511 | ||||||
| chr12:59631583
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-23569G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59631583 | ||||||
| chr12:59632193
|
A | G | 1 | a0002c0002t0003g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-129-22959A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632193 | ||||||
| chr12:59632270
|
G | A | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-22882G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632270 | ||||||
| chr12:59632272
|
A | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-22880A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632272 | ||||||
| chr12:59632307
|
G | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-129-22845G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632307 | ||||||
| chr12:59632318
|
GA | G | 4 | a0002c0002t0003g0085a0002c0002t0003g0169a0002c0002t0003g0170others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-22831delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59632318 | |||||
| chr12:59632463
|
G | A | 2 | a0001c0001t0002g0173a0001c0001t0038g0062 | 2 | HG00280.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-129-22689G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632463 | ||||||
| chr12:59632921
|
AT | A | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-22230delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632921 | ||||||
| chr12:59632939
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-129-22213C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632939 | ||||||
| chr12:59632940
|
G | A | 16 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-129-22212G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59632940 | ||||||
| chr12:59633054
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-129-22098T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633054 | ||||||
| chr12:59633224
|
G | A | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-129-21928G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633224 | ||||||
| chr12:59633340
|
T | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-21812T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633340 | ||||||
| chr12:59633408
|
T | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-129-21744T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633408 | ||||||
| chr12:59633430
|
T | G | 16 | a0001c0001t0001g0113a0001c0001t0006g0171a0001c0001t0006g0226others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.-129-21722T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633430 | ||||||
| chr12:59633540
|
A | G | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-21612A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633540 | ||||||
| chr12:59633644
|
GA | G | 6 | a0001c0001t0002g0140a0001c0001t0009g0243a0001c0001t0020g0006others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-129-21496delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59633644 | |||||
| chr12:59633741
|
G | A | 1 | a0001c0001t0007g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-129-21411G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633741 | ||||||
| chr12:59633796
|
C | T | 1 | a0001c0001t0044g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-129-21356C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633796 | ||||||
| chr12:59633829
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-21323C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633829 | ||||||
| chr12:59633927
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0200 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-129-21225G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59633927 | ||||||
| chr12:59634023
|
C | G | 1 | a0002c0002t0023g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-129-21129C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634023 | ||||||
| chr12:59634082
|
A | G | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-21070A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634082 | ||||||
| chr12:59634109
|
G | A | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-129-21043G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634109 | ||||||
| chr12:59634188
|
A | T | 3 | a0001c0001t0043g0047a0001c0001t0046g0002a0001c0001t0048g0081 | 3 | HG02145.hp2 HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-129-20964A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634188 | ||||||
| chr12:59634330
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-129-20822A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634330 | ||||||
| chr12:59634383
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0007g0031 | 3 | HG01928.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-129-20769C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634383 | ||||||
| chr12:59634422
|
A | T | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-129-20730A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634422 | ||||||
| chr12:59634640
|
T | C | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-129-20512T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634640 | ||||||
| chr12:59634717
|
A | G | 1 | a0008c0007t0003g0045 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-129-20435A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634717 | ||||||
| chr12:59634915
|
G | T | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-129-20237G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59634915 | ||||||
| chr12:59635161
|
A | T | 1 | a0001c0001t0002g0057 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-129-19991A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635161 | ||||||
| chr12:59635173
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-129-19979T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635173 | ||||||
| chr12:59635272
|
T | C | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-129-19880T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635272 | ||||||
| chr12:59635308
|
T | G | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-19844T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635308 | ||||||
| chr12:59635500
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-19652C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635500 | ||||||
| chr12:59635591
|
G | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-19561G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635591 | ||||||
| chr12:59635778
|
T | C | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-129-19374T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635778 | ||||||
| chr12:59635935
|
C | G | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-129-19217C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59635935 | ||||||
| chr12:59636002
|
TA | T | 114 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-129-19133delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59636002 | |||||
| chr12:59636002
|
TAA | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0041others(124): Show | 127 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-129-19134_-129-19 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59636002 | |||||
| chr12:59636002
|
TAAAA | T | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-19136_-129-19 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59636002 | |||||
| chr12:59636135
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-129-19017G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59636135 | ||||||
| chr12:59636191
|
C | T | 34 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(31): Show | 34 | HG00597.hp2 HG00609.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.-129-18961C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59636191 | ||||||
| chr12:59636547
|
C | G | 21 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-129-18605C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59636547 | ||||||
| chr12:59636817
|
G | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-18335G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59636817 | ||||||
| chr12:59636832
|
C | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-129-18320C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59636832 | ||||||
| chr12:59636961
|
T | TCACTGAC others(14): Show |
1 | a0001c0003t0010g0019 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-129-18189_-129-18 others(27): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59636961 | |||||
| chr12:59637120
|
G | A | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-18032G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637120 | ||||||
| chr12:59637240
|
A | C | 1 | a0002c0002t0003g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-129-17912A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637240 | ||||||
| chr12:59637703
|
T | C | 7 | a0001c0001t0006g0001a0001c0001t0009g0243a0001c0001t0020g0006others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-129-17449T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637703 | ||||||
| chr12:59637825
|
C | T | 1 | a0001c0001t0033g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-129-17327C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637825 | ||||||
| chr12:59637890
|
C | T | 14 | a0001c0001t0011g0144a0002c0002t0003g0106a0002c0002t0003g0107others(11): Show | 14 | HG00423.hp1 HG00597.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-129-17262C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637890 | ||||||
| chr12:59637980
|
T | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0200 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-129-17172T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59637980 | ||||||
| chr12:59638025
|
G | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-129-17127G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638025 | ||||||
| chr12:59638121
|
C | A | 2 | a0002c0002t0003g0122a0002c0002t0003g0190 | 2 | HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-129-17031C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638121 | ||||||
| chr12:59638129
|
A | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-17023A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638129 | ||||||
| chr12:59638455
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-16697A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638455 | ||||||
| chr12:59638627
|
A | G | 1 | a0002c0002t0004g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-129-16525A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638627 | ||||||
| chr12:59638648
|
G | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-16504G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638648 | ||||||
| chr12:59638724
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0034g0084 | 3 | HG00099.hp2 HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-129-16428A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638724 | ||||||
| chr12:59638754
|
C | T | 1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-129-16398C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638754 | ||||||
| chr12:59638771
|
T | A | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-16381T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638771 | ||||||
| chr12:59638969
|
A | T | 1 | a0002c0002t0003g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-129-16183A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59638969 | ||||||
| chr12:59639029
|
A | AT | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-16117dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59639029 | |||||
| chr12:59639039
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-129-16113A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639039 | ||||||
| chr12:59639232
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-15920A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639232 | ||||||
| chr12:59639294
|
C | T | 11 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(8): Show | 11 | HG00597.hp2 HG01175.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129-15858C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639294 | ||||||
| chr12:59639483
|
A | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-129-15669A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639483 | ||||||
| chr12:59639492
|
T | G | 2 | a0001c0001t0006g0172a0001c0001t0006g0207 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-129-15660T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639492 | ||||||
| chr12:59639528
|
T | G | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-129-15624T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639528 | ||||||
| chr12:59639569
|
A | G | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-15583A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59639569 | ||||||
| chr12:59640249
|
T | C | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-14903T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640249 | ||||||
| chr12:59640258
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-14894C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640258 | ||||||
| chr12:59640426
|
G | GC | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-129-14719dupC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59640426 | |||||
| chr12:59640433
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-129-14719C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640433 | ||||||
| chr12:59640521
|
G | GA | 133 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(130): Show | 133 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-129-14626dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59640521 | |||||
| chr12:59640527
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(130): Show | 133 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-129-14625G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640527 | ||||||
| chr12:59640595
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-14557C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640595 | ||||||
| chr12:59640778
|
C | T | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-129-14374C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640778 | ||||||
| chr12:59640910
|
G | A | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-14242G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640910 | ||||||
| chr12:59640942
|
A | G | 1 | a0001c0001t0010g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-129-14210A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59640942 | ||||||
| chr12:59641009
|
A | G | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-14143A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641009 | ||||||
| chr12:59641051
|
T | C | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-14101T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641051 | ||||||
| chr12:59641098
|
C | T | 1 | a0001c0001t0026g0042 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-129-14054C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641098 | ||||||
| chr12:59641207
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-13945C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641207 | ||||||
| chr12:59641356
|
A | C | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-129-13796A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641356 | ||||||
| chr12:59641490
|
T | C | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-13662T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641490 | ||||||
| chr12:59641557
|
A | AT | 6 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(3): Show | 6 | HG01175.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129-13586dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59641557 | |||||
| chr12:59641557
|
AT | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(113): Show | 116 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-129-13586delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59641557 | |||||
| chr12:59641600
|
G | A | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-13552G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641600 | ||||||
| chr12:59641661
|
A | G | 2 | a0001c0001t0002g0146a0002c0002t0003g0147 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-129-13491A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641661 | ||||||
| chr12:59641704
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-129-13448T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641704 | ||||||
| chr12:59641774
|
G | A | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-129-13378G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641774 | ||||||
| chr12:59641837
|
T | C | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-13315T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641837 | ||||||
| chr12:59641843
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-129-13309C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641843 | ||||||
| chr12:59641850
|
C | T | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-13302C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641850 | ||||||
| chr12:59641930
|
A | G | 5 | a0001c0001t0009g0243a0001c0001t0020g0006a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-13222A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59641930 | ||||||
| chr12:59642438
|
A | G | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-12714A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59642438 | ||||||
| chr12:59642907
|
T | C | 1 | a0002c0002t0003g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-129-12245T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59642907 | ||||||
| chr12:59642937
|
G | T | 4 | a0001c0001t0002g0065a0001c0001t0007g0199a0001c0001t0011g0178others(1): Show | 4 | HG00673.hp1 NA18995.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-12215G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59642937 | ||||||
| chr12:59643111
|
C | T | 2 | a0001c0001t0010g0237a0002c0002t0003g0114 | 2 | HG01123.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-129-12041C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643111 | ||||||
| chr12:59643179
|
T | C | 6 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(3): Show | 6 | HG01175.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129-11973T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643179 | ||||||
| chr12:59643340
|
T | C | 1 | a0002c0002t0003g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-129-11812T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643340 | ||||||
| chr12:59643365
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(7): Show | 10 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-129-11787G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643365 | ||||||
| chr12:59643785
|
A | G | 1 | a0001c0001t0026g0042 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-129-11367A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643785 | ||||||
| chr12:59643825
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-129-11327C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643825 | ||||||
| chr12:59643989
|
T | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-129-11163T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59643989 | ||||||
| chr12:59644072
|
G | C | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-11080G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644072 | ||||||
| chr12:59644126
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-11026G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644126 | ||||||
| chr12:59644154
|
G | C | 26 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(23): Show | 26 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-129-10998G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644154 | ||||||
| chr12:59644173
|
T | TA | 138 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(135): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-129-10972dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59644173 | |||||
| chr12:59644211
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-129-10941T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644211 | ||||||
| chr12:59644213
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-129-10939T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644213 | ||||||
| chr12:59644237
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-10915G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644237 | ||||||
| chr12:59644335
|
G | A | 4 | a0002c0002t0004g0036a0002c0002t0004g0136a0002c0002t0004g0137others(1): Show | 4 | NA18940.hp2 NA18957.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-10817G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644335 | ||||||
| chr12:59644336
|
G | C | 1 | a0001c0003t0005g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-129-10816G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644336 | ||||||
| chr12:59644358
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(7): Show | 10 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-129-10794G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644358 | ||||||
| chr12:59644601
|
C | T | 1 | a0002c0002t0004g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-129-10551C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644601 | ||||||
| chr12:59644690
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0032others(1): Show | 4 | HG01928.hp2 HG02148.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-10462A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644690 | ||||||
| chr12:59644898
|
A | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-129-10254A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59644898 | ||||||
| chr12:59645438
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-129-9714T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645438 | ||||||
| chr12:59645491
|
C | T | 1 | a0001c0001t0012g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-129-9661C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645491 | ||||||
| chr12:59645506
|
G | A | 5 | a0001c0001t0002g0146a0002c0002t0003g0060a0002c0002t0003g0147others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-9646G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645506 | ||||||
| chr12:59645512
|
G | T | 23 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(20): Show | 23 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-129-9640G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645512 | ||||||
| chr12:59645604
|
C | T | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-129-9548C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645604 | ||||||
| chr12:59645646
|
A | G | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-9506A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645646 | ||||||
| chr12:59645790
|
G | C | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-9362G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645790 | ||||||
| chr12:59645881
|
A | T | 26 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(23): Show | 26 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-129-9271A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645881 | ||||||
| chr12:59645952
|
T | G | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-129-9200T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59645952 | ||||||
| chr12:59646266
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-129-8886T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646266 | ||||||
| chr12:59646287
|
C | A | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-129-8865C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646287 | ||||||
| chr12:59646294
|
G | A | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-8858G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646294 | ||||||
| chr12:59646317
|
A | T | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-129-8835A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646317 | ||||||
| chr12:59646481
|
A | G | 1 | a0002c0002t0004g0230 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-129-8671A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646481 | ||||||
| chr12:59646517
|
G | A | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129-8635G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646517 | ||||||
| chr12:59646546
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-129-8606A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646546 | ||||||
| chr12:59646889
|
G | A | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-129-8263G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646889 | ||||||
| chr12:59646986
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-129-8166C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59646986 | ||||||
| chr12:59647015
|
T | C | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-8137T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647015 | ||||||
| chr12:59647122
|
C | T | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-129-8030C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647122 | ||||||
| chr12:59647123
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-129-8029G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647123 | ||||||
| chr12:59647182
|
G | A | 2 | a0002c0002t0003g0107a0002c0002t0003g0183 | 2 | HG00423.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-129-7970G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647182 | ||||||
| chr12:59647187
|
G | A | 1 | a0002c0002t0003g0156 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-129-7965G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647187 | ||||||
| chr12:59647273
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-129-7879A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647273 | ||||||
| chr12:59647441
|
T | C | 4 | a0002c0002t0003g0008a0002c0002t0003g0110a0002c0002t0003g0111others(1): Show | 4 | HG01496.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-7711T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647441 | ||||||
| chr12:59647618
|
G | GA | 111 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-129-7532dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59647618 | |||||
| chr12:59647696
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-129-7456T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647696 | ||||||
| chr12:59647707
|
T | C | 2 | a0001c0001t0046g0002a0001c0001t0048g0081 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-129-7445T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647707 | ||||||
| chr12:59647805
|
G | A | 7 | a0001c0001t0009g0243a0001c0001t0013g0259a0001c0001t0015g0258others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-129-7347G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59647805 | ||||||
| chr12:59647885
|
CA | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129-7257delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59647885 | |||||
| chr12:59648102
|
G | T | 2 | a0001c0001t0010g0035a0008c0007t0003g0045 | 2 | NA19062.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-129-7050G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648102 | ||||||
| chr12:59648151
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-129-7001T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648151 | ||||||
| chr12:59648174
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-6978C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648174 | ||||||
| chr12:59648206
|
C | T | 1 | a0001c0003t0005g0012 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-129-6946C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648206 | ||||||
| chr12:59648422
|
A | C | 15 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(12): Show | 15 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-129-6730A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648422 | ||||||
| chr12:59648879
|
G | A | 1 | a0001c0001t0018g0005 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-129-6273G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59648879 | ||||||
| chr12:59649246
|
G | A | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-129-5906G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649246 | ||||||
| chr12:59649341
|
G | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-5811G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649341 | ||||||
| chr12:59649688
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-129-5464C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649688 | ||||||
| chr12:59649733
|
G | C | 23 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(20): Show | 23 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-129-5419G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649733 | ||||||
| chr12:59649951
|
C | G | 2 | a0001c0003t0005g0141a0002c0002t0017g0182 | 2 | HG00609.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-129-5201C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649951 | ||||||
| chr12:59649957
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-129-5195C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59649957 | ||||||
| chr12:59650059
|
G | A | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-129-5093G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650059 | ||||||
| chr12:59650151
|
T | C | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-129-5001T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650151 | ||||||
| chr12:59650240
|
G | A | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-4912G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650240 | ||||||
| chr12:59650308
|
G | A | 5 | a0001c0001t0043g0047a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-4844G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650308 | ||||||
| chr12:59650348
|
A | C | 1 | a0001c0001t0012g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-129-4804A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650348 | ||||||
| chr12:59650549
|
G | A | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-4603G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650549 | ||||||
| chr12:59650663
|
A | G | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-4489A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650663 | ||||||
| chr12:59650746
|
G | A | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-129-4406G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59650746 | ||||||
| chr12:59651149
|
A | G | 5 | a0001c0001t0043g0047a0002c0002t0003g0085a0002c0002t0003g0169others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-4003A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651149 | ||||||
| chr12:59651213
|
T | G | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-3939T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651213 | ||||||
| chr12:59651325
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-129-3827G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651325 | ||||||
| chr12:59651422
|
G | A | 4 | a0002c0002t0003g0085a0002c0002t0003g0169a0002c0002t0003g0170others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-3730G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651422 | ||||||
| chr12:59651455
|
T | C | 1 | a0001c0003t0005g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-129-3697T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651455 | ||||||
| chr12:59651790
|
C | T | 2 | a0001c0003t0005g0203a0007c0008t0040g0151 | 2 | HG03669.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-129-3362C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651790 | ||||||
| chr12:59651801
|
G | A | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-3351G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651801 | ||||||
| chr12:59651838
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-129-3314C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59651838 | ||||||
| chr12:59652188
|
ATAAGT | A | 14 | a0002c0002t0003g0106a0002c0002t0003g0107a0002c0002t0003g0120others(11): Show | 14 | HG00423.hp1 HG00597.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-129-2960_-129-295 others(9): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59652188 | |||||
| chr12:59652400
|
G | T | 4 | a0002c0002t0004g0036a0002c0002t0004g0136a0002c0002t0004g0137others(1): Show | 4 | NA18940.hp2 NA18957.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-2752G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59652400 | ||||||
| chr12:59652491
|
T | C | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129-2661T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59652491 | ||||||
| chr12:59652972
|
T | G | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-129-2180T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59652972 | ||||||
| chr12:59653103
|
T | C | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-2049T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653103 | ||||||
| chr12:59653238
|
A | G | 30 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(27): Show | 30 | HG00597.hp2 HG01261.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-129-1914A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653238 | ||||||
| chr12:59653405
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0037others(6): Show | 9 | HG00673.hp2 HG01123.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129-1747T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653405 | ||||||
| chr12:59653497
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-129-1655G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653497 | ||||||
| chr12:59653534
|
A | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-129-1618A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653534 | ||||||
| chr12:59653550
|
G | A | 5 | a0001c0001t0002g0146a0002c0002t0003g0060a0002c0002t0003g0147others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129-1602G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653550 | ||||||
| chr12:59653576
|
A | C | 1 | a0002c0002t0003g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-129-1576A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653576 | ||||||
| chr12:59653738
|
A | C | 1 | a0001c0003t0005g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-129-1414A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653738 | ||||||
| chr12:59653988
|
A | T | 1 | a0001c0001t0002g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-129-1164A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59653988 | ||||||
| chr12:59654097
|
GTTA | G | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-129-1048_-129-104 others(7): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59654097 | |||||
| chr12:59654206
|
G | T | 4 | a0002c0002t0003g0008a0002c0002t0003g0110a0002c0002t0003g0111others(1): Show | 4 | HG01496.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-946G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59654206 | ||||||
| chr12:59654376
|
T | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-129-776T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59654376 | ||||||
| chr12:59654704
|
C | CACAT | 111 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-129-445_-129-444i others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 59654704 | |||||
| chr12:59654821
|
T | C | 30 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(27): Show | 30 | HG00597.hp2 HG01261.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-129-331T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59654821 | ||||||
| chr12:59655077
|
G | A | 4 | a0002c0002t0003g0085a0002c0002t0003g0169a0002c0002t0003g0170others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129-75G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59655077 | ||||||
| chr12:59655108
|
C | A | 4 | a0002c0002t0003g0008a0002c0002t0003g0110a0002c0002t0003g0111others(1): Show | 4 | HG01496.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129-44C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 1/5 | chr12 | 59655108 | ||||||
| chr12:59655643
|
A | T | 4 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0118others(1): Show | 4 | HG01257.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+393A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655643 | ||||||
| chr12:59655662
|
A | C | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+412A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655662 | ||||||
| chr12:59655707
|
G | T | 20 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+457G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655707 | ||||||
| chr12:59655717
|
G | A | 3 | a0001c0001t0013g0259a0001c0001t0015g0258a0002c0002t0024g0034 | 3 | HG02451.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-31+467G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655717 | ||||||
| chr12:59655796
|
CT | C | 7 | a0001c0001t0009g0243a0001c0001t0013g0259a0001c0001t0015g0258others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+548delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59655796 | |||||
| chr12:59655830
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+580G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655830 | ||||||
| chr12:59655968
|
A | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+718A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59655968 | ||||||
| chr12:59656165
|
T | C | 7 | a0001c0001t0009g0243a0001c0001t0013g0259a0001c0001t0015g0258others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+915T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656165 | ||||||
| chr12:59656284
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-31+1034G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656284 | ||||||
| chr12:59656712
|
G | A | 1 | a0001c0001t0006g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-31+1462G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656712 | ||||||
| chr12:59656794
|
C | T | 16 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+1544C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656794 | ||||||
| chr12:59656878
|
A | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+1628A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656878 | ||||||
| chr12:59656908
|
G | A | 2 | a0002c0002t0003g0008a0002c0002t0003g0228 | 2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-31+1658G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656908 | ||||||
| chr12:59656951
|
G | A | 16 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+1701G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59656951 | ||||||
| chr12:59657036
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-31+1786A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657036 | ||||||
| chr12:59657354
|
A | G | 1 | a0001c0001t0012g0254 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-31+2104A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657354 | ||||||
| chr12:59657434
|
G | C | 23 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(20): Show | 23 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+2184G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657434 | ||||||
| chr12:59657654
|
G | A | 1 | a0001c0001t0007g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-31+2404G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657654 | ||||||
| chr12:59657792
|
G | A | 21 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0124others(18): Show | 21 | HG00408.hp2 HG00735.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+2542G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657792 | ||||||
| chr12:59657886
|
C | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+2636C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657886 | ||||||
| chr12:59657961
|
T | C | 1 | a0001c0003t0005g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-31+2711T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59657961 | ||||||
| chr12:59658162
|
G | A | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-31+2912G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658162 | ||||||
| chr12:59658361
|
G | A | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+3111G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658361 | ||||||
| chr12:59658571
|
C | G | 4 | a0001c0001t0002g0065a0001c0001t0007g0199a0001c0001t0011g0178others(1): Show | 4 | HG00673.hp1 NA18995.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+3321C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658571 | ||||||
| chr12:59658619
|
C | T | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31+3369C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658619 | ||||||
| chr12:59658794
|
C | T | 2 | a0002c0002t0003g0085a0002c0002t0008g0088 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-31+3544C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658794 | ||||||
| chr12:59658822
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-31+3572A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658822 | ||||||
| chr12:59658942
|
A | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0111 | 2 | HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-31+3692A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658942 | ||||||
| chr12:59658979
|
G | A | 11 | a0001c0001t0002g0051a0001c0001t0002g0193a0001c0001t0002g0210others(8): Show | 11 | HG00423.hp2 HG02040.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+3729G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59658979 | ||||||
| chr12:59659010
|
A | T | 2 | a0001c0001t0013g0259a0001c0001t0015g0258 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-31+3760A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659010 | ||||||
| chr12:59659128
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+3878C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659128 | ||||||
| chr12:59659210
|
A | G | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-31+3960A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659210 | ||||||
| chr12:59659251
|
G | T | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+4001G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659251 | ||||||
| chr12:59659316
|
T | C | 2 | a0001c0001t0006g0001a0006c0010t0020g0108 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-31+4066T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659316 | ||||||
| chr12:59659475
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-31+4225G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659475 | ||||||
| chr12:59659581
|
G | T | 1 | a0001c0001t0002g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-31+4331G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659581 | ||||||
| chr12:59659589
|
A | G | 1 | a0005c0009t0003g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-31+4339A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659589 | ||||||
| chr12:59659886
|
C | G | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+4636C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659886 | ||||||
| chr12:59659935
|
C | A | 7 | a0001c0001t0009g0243a0001c0001t0013g0259a0001c0001t0015g0258others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+4685C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659935 | ||||||
| chr12:59659989
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-31+4739A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59659989 | ||||||
| chr12:59660156
|
A | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+4906A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660156 | ||||||
| chr12:59660284
|
C | T | 23 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(20): Show | 23 | HG00597.hp2 HG01261.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+5034C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660284 | ||||||
| chr12:59660297
|
C | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+5047C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660297 | ||||||
| chr12:59660541
|
C | CA | 80 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-31+5307dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59660541 | |||||
| chr12:59660541
|
C | CAA | 9 | a0001c0001t0009g0243a0001c0001t0013g0259a0001c0001t0015g0258others(6): Show | 9 | HG02080.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+5306_-31+5307d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59660541 | |||||
| chr12:59660558
|
T | A | 1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-31+5308T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660558 | ||||||
| chr12:59660583
|
A | G | 6 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0042g0252others(3): Show | 6 | HG02109.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5333A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660583 | ||||||
| chr12:59660767
|
T | G | 10 | a0001c0001t0006g0001a0001c0001t0009g0243a0001c0001t0013g0259others(7): Show | 10 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+5517T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660767 | ||||||
| chr12:59660888
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+5638G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59660888 | ||||||
| chr12:59661033
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+5783C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661033 | ||||||
| chr12:59661167
|
T | G | 3 | a0001c0001t0013g0259a0001c0001t0015g0258a0001c0001t0020g0006 | 3 | HG02451.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+5917T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661167 | ||||||
| chr12:59661257
|
C | A | 7 | a0001c0001t0043g0047a0001c0001t0046g0002a0001c0001t0048g0081others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+6007C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661257 | ||||||
| chr12:59661272
|
A | G | 5 | a0002c0002t0004g0036a0002c0002t0004g0136a0002c0002t0004g0137others(2): Show | 5 | NA18940.hp2 NA18957.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+6022A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661272 | ||||||
| chr12:59661308
|
A | T | 2 | a0001c0001t0006g0253a0001c0001t0007g0097 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-31+6058A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661308 | ||||||
| chr12:59661668
|
C | G | 18 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+6418C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661668 | ||||||
| chr12:59661682
|
A | G | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-31+6432A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661682 | ||||||
| chr12:59661719
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-31+6469A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661719 | ||||||
| chr12:59661727
|
G | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0180a0001c0001t0001g0208 | 3 | NA18947.hp1 NA18979.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-31+6477G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661727 | ||||||
| chr12:59661796
|
A | G | 2 | a0002c0002t0003g0169a0002c0002t0003g0170 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31+6546A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661796 | ||||||
| chr12:59661841
|
T | A | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31+6591T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661841 | ||||||
| chr12:59661854
|
C | T | 20 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+6604C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661854 | ||||||
| chr12:59661907
|
A | G | 4 | a0001c0001t0041g0232a0001c0001t0043g0047a0002c0002t0003g0085others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+6657A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661907 | ||||||
| chr12:59661989
|
A | G | 1 | a0001c0001t0006g0167 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+6739A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59661989 | ||||||
| chr12:59662022
|
A | AT | 97 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+6772_-31+6773i others(3): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662022 | ||||||
| chr12:59662109
|
A | C | 1 | a0001c0001t0028g0133 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-31+6859A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662109 | ||||||
| chr12:59662115
|
G | A | 6 | a0001c0001t0018g0005a0002c0002t0004g0036a0002c0002t0004g0136others(3): Show | 6 | NA18940.hp2 NA18957.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+6865G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662115 | ||||||
| chr12:59662136
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-31+6886T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662136 | ||||||
| chr12:59662391
|
T | C | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+7141T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662391 | ||||||
| chr12:59662453
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+7203C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662453 | ||||||
| chr12:59662474
|
G | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+7224G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662474 | ||||||
| chr12:59662676
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+7426C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662676 | ||||||
| chr12:59662817
|
A | G | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-31+7567A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662817 | ||||||
| chr12:59662904
|
G | C | 4 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+7654G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59662904 | ||||||
| chr12:59663365
|
TA | T | 83 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-31+8122delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59663365 | |||||
| chr12:59663490
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00639.hp1 HG00738.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-31+8240T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663490 | ||||||
| chr12:59663493
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-31+8243C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663493 | ||||||
| chr12:59663586
|
T | C | 4 | a0001c0001t0006g0221a0001c0001t0006g0222a0001c0001t0006g0225others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+8336T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663586 | ||||||
| chr12:59663604
|
A | T | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+8354A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663604 | ||||||
| chr12:59663685
|
G | A | 3 | a0001c0001t0013g0259a0001c0001t0015g0258a0001c0001t0020g0006 | 3 | HG02451.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+8435G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663685 | ||||||
| chr12:59663766
|
A | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+8516A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663766 | ||||||
| chr12:59663965
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-31+8715T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663965 | ||||||
| chr12:59663973
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-31+8723A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59663973 | ||||||
| chr12:59664106
|
CTT | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8857_-31+8858d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664106 | ||||||
| chr12:59664109
|
A | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8859A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664109 | ||||||
| chr12:59664114
|
A | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8864A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664114 | ||||||
| chr12:59664115
|
G | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8865G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664115 | ||||||
| chr12:59664116
|
TAATCAA | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8869_-31+8874d others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59664116 | |||||
| chr12:59664123
|
A | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0209 | 3 | HG02165.hp2 NA18983.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-31+8873A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664123 | ||||||
| chr12:59664125
|
C | T | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31+8875C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664125 | ||||||
| chr12:59664145
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+8895A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664145 | ||||||
| chr12:59664171
|
A | G | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31+8921A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664171 | ||||||
| chr12:59664239
|
A | G | 8 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0045g0013others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+8989A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664239 | ||||||
| chr12:59664478
|
T | C | 2 | a0001c0001t0041g0232a0001c0001t0043g0047 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+9228T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664478 | ||||||
| chr12:59664589
|
G | T | 18 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+9339G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664589 | ||||||
| chr12:59664668
|
G | T | 1 | a0001c0001t0006g0225 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-31+9418G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664668 | ||||||
| chr12:59664760
|
G | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0175a0001c0001t0028g0133 | 3 | NA18969.hp1 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-31+9510G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664760 | ||||||
| chr12:59664920
|
A | G | 1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-31+9670A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59664920 | ||||||
| chr12:59665377
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-31+10127A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59665377 | ||||||
| chr12:59665654
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+10404C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59665654 | ||||||
| chr12:59665750
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+10500T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59665750 | ||||||
| chr12:59665809
|
C | CGT | 12 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0039others(9): Show | 12 | HG00621.hp2 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.-31+10592_-31+1059 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59665809 | |||||
| chr12:59665809
|
C | CGTGT | 13 | a0001c0001t0002g0152a0001c0001t0006g0001a0001c0001t0006g0171others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+10590_-31+1059 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59665809 | |||||
| chr12:59665809
|
CGT | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(102): Show | 105 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-31+10592_-31+1059 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59665809 | |||||
| chr12:59665809
|
CGTGT | C | 8 | a0001c0001t0001g0175a0001c0001t0002g0210a0001c0001t0006g0167others(5): Show | 8 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+10590_-31+1059 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59665809 | |||||
| chr12:59665968
|
T | C | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+10718T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59665968 | ||||||
| chr12:59666054
|
A | G | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+10804A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666054 | ||||||
| chr12:59666075
|
G | A | 4 | a0001c0003t0005g0141a0001c0003t0005g0235a0001c0003t0005g0236others(1): Show | 4 | HG01261.hp2 HG03239.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+10825G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666075 | ||||||
| chr12:59666157
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-31+10907A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666157 | ||||||
| chr12:59666241
|
A | G | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-31+10991A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666241 | ||||||
| chr12:59666264
|
C | T | 1 | a0001c0001t0021g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+11014C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666264 | ||||||
| chr12:59666303
|
G | A | 1 | a0002c0002t0017g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-31+11053G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666303 | ||||||
| chr12:59666339
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-31+11089C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666339 | ||||||
| chr12:59666345
|
T | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+11095T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666345 | ||||||
| chr12:59666494
|
G | A | 6 | a0001c0001t0009g0243a0001c0001t0025g0248a0001c0001t0042g0252others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+11244G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666494 | ||||||
| chr12:59666708
|
C | A | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+11458C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666708 | ||||||
| chr12:59666762
|
C | A | 3 | a0001c0001t0002g0055a0001c0001t0007g0052a0001c0001t0007g0064 | 3 | HG01928.hp1 HG01978.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-31+11512C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666762 | ||||||
| chr12:59666838
|
G | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+11588G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666838 | ||||||
| chr12:59666859
|
A | G | 84 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-31+11609A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666859 | ||||||
| chr12:59666919
|
G | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+11669G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666919 | ||||||
| chr12:59666950
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(174): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-31+11700A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59666950 | ||||||
| chr12:59667046
|
A | G | 1 | a0002c0002t0004g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-31+11796A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667046 | ||||||
| chr12:59667195
|
C | T | 2 | a0001c0003t0005g0216a0002c0002t0004g0077 | 2 | HG00558.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.-31+11945C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667195 | ||||||
| chr12:59667220
|
A | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(173): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-31+11970A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667220 | ||||||
| chr12:59667279
|
A | G | 18 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+12029A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667279 | ||||||
| chr12:59667345
|
T | C | 1 | a0001c0001t0007g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-31+12095T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667345 | ||||||
| chr12:59667461
|
G | T | 1 | a0002c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-31+12211G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667461 | ||||||
| chr12:59667716
|
A | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+12466A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667716 | ||||||
| chr12:59667912
|
C | T | 2 | a0001c0001t0041g0232a0001c0001t0043g0047 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+12662C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667912 | ||||||
| chr12:59667923
|
A | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 74 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-31+12673A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59667923 | ||||||
| chr12:59668027
|
G | A | 1 | a0001c0001t0013g0259 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-31+12777G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668027 | ||||||
| chr12:59668115
|
G | A | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-31+12865G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668115 | ||||||
| chr12:59668215
|
C | T | 2 | a0002c0002t0003g0085a0002c0002t0008g0088 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-31+12965C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668215 | ||||||
| chr12:59668269
|
C | T | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+13019C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668269 | ||||||
| chr12:59668402
|
T | C | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+13152T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668402 | ||||||
| chr12:59668422
|
G | T | 18 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+13172G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668422 | ||||||
| chr12:59668524
|
G | A | 1 | a0001c0001t0035g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-31+13274G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668524 | ||||||
| chr12:59668698
|
C | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+13448C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668698 | ||||||
| chr12:59668777
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-31+13527C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668777 | ||||||
| chr12:59668972
|
C | A | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+13722C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59668972 | ||||||
| chr12:59669004
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-31+13754A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669004 | ||||||
| chr12:59669048
|
C | A | 1 | a0002c0002t0004g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-31+13798C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669048 | ||||||
| chr12:59669124
|
A | T | 1 | a0002c0002t0003g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-31+13874A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669124 | ||||||
| chr12:59669167
|
A | T | 1 | a0001c0001t0033g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-31+13917A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669167 | ||||||
| chr12:59669193
|
T | C | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31+13943T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669193 | ||||||
| chr12:59669378
|
T | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0118a0001c0001t0013g0069 | 3 | HG02109.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+14128T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669378 | ||||||
| chr12:59669569
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+14319C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669569 | ||||||
| chr12:59669652
|
T | TCA | 107 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-31+14434_-31+1443 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACA | 8 | a0001c0001t0001g0048a0001c0001t0001g0079a0001c0001t0002g0014others(5): Show | 8 | HG02717.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+14432_-31+1443 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACA | 4 | a0001c0001t0006g0001a0001c0001t0009g0243a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+14430_-31+1443 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0006g0029others(5): Show | 8 | HG00609.hp1 HG01358.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+14428_-31+1443 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0015g0004 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-31+14426_-31+1443 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(5): Show |
18 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 18 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+14424_-31+1443 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(7): Show |
5 | a0001c0001t0002g0224a0001c0001t0006g0222a0001c0001t0034g0084others(2): Show | 5 | HG00099.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+14422_-31+1443 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(9): Show |
11 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG00280.hp1 HG01257.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+14420_-31+1443 others(20): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(11): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0046others(4): Show | 7 | HG01928.hp2 HG02300.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+14418_-31+1443 others(22): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(13): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0104a0001c0001t0001g0220others(1): Show | 4 | HG02698.hp1 HG03130.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+14416_-31+1443 others(24): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(15): Show |
16 | a0001c0001t0001g0021a0001c0001t0002g0101a0001c0001t0006g0171others(13): Show | 16 | HG01175.hp1 HG02109.hp2 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+14414_-31+1443 others(26): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(17): Show |
5 | a0001c0001t0002g0119a0001c0001t0002g0160a0001c0001t0002g0161others(2): Show | 5 | HG01261.hp2 HG02886.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+14412_-31+1443 others(28): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(19): Show |
3 | a0001c0001t0002g0202a0001c0001t0006g0221a0002c0002t0004g0231 | 3 | HG00597.hp2 HG02615.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+14410_-31+1443 others(30): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669652
|
T | TCACACAC others(23): Show |
1 | a0001c0001t0014g0145 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-31+14406_-31+1443 others(34): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669652 | |||||
| chr12:59669699
|
G | A | 1 | a0001c0003t0005g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-31+14449G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669699 | ||||||
| chr12:59669784
|
G | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-31+14534G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669784 | ||||||
| chr12:59669851
|
AT | A | 7 | a0001c0001t0006g0117a0001c0001t0006g0159a0001c0001t0006g0167others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+14603delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59669851 | |||||
| chr12:59669985
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+14735C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59669985 | ||||||
| chr12:59670017
|
T | G | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+14767T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670017 | ||||||
| chr12:59670085
|
G | T | 4 | a0001c0001t0010g0123a0001c0001t0010g0237a0001c0003t0010g0019others(1): Show | 4 | HG00639.hp2 HG01123.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+14835G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670085 | ||||||
| chr12:59670113
|
C | A | 1 | a0002c0002t0003g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-31+14863C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670113 | ||||||
| chr12:59670142
|
C | A | 57 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-31+14892C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670142 | ||||||
| chr12:59670251
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+15001G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670251 | ||||||
| chr12:59670296
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-31+15046G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670296 | ||||||
| chr12:59670304
|
G | A | 40 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-31+15054G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670304 | ||||||
| chr12:59670410
|
AT | A | 10 | a0001c0001t0002g0051a0001c0001t0002g0193a0001c0001t0002g0210others(7): Show | 10 | HG00423.hp2 HG02040.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31+15161delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670410 | ||||||
| chr12:59670602
|
C | T | 1 | a0001c0003t0005g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-31+15352C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670602 | ||||||
| chr12:59670687
|
A | C | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+15437A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670687 | ||||||
| chr12:59670702
|
G | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+15452G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670702 | ||||||
| chr12:59670731
|
A | C | 10 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0045g0013others(7): Show | 10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+15481A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670731 | ||||||
| chr12:59670786
|
G | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+15536G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670786 | ||||||
| chr12:59670916
|
A | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-31+15666A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670916 | ||||||
| chr12:59670931
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+15681G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59670931 | ||||||
| chr12:59671105
|
C | A | 1 | a0002c0002t0008g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-31+15855C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671105 | ||||||
| chr12:59671286
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+16036T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671286 | ||||||
| chr12:59671419
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(173): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-31+16169T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671419 | ||||||
| chr12:59671499
|
A | ATATGCAC others(4): Show |
1 | a0001c0001t0007g0139 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-31+16251_-31+1626 others(15): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671499 | |||||
| chr12:59671622
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+16372A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671622 | ||||||
| chr12:59671658
|
TTC | T | 16 | a0001c0001t0002g0051a0001c0001t0006g0117a0001c0001t0006g0159others(13): Show | 16 | HG00597.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+16428_-31+1642 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671658 | |||||
| chr12:59671674
|
C | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0025others(14): Show | 17 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-31+16424C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671674 | ||||||
| chr12:59671676
|
C | A | 36 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-31+16426C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671676 | ||||||
| chr12:59671678
|
C | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-31+16428C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671678 | ||||||
| chr12:59671678
|
CTA | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-31+16440_-31+1644 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671678 | |||||
| chr12:59671680
|
A | C | 49 | a0001c0001t0001g0155a0001c0001t0001g0194a0001c0001t0002g0011others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-31+16430A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671680 | ||||||
| chr12:59671682
|
A | C | 3 | a0001c0001t0002g0082a0001c0001t0002g0086a0002c0002t0003g0186 | 3 | HG01109.hp2 HG02155.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-31+16432A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671682 | ||||||
| chr12:59671690
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+16440A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671690 | ||||||
| chr12:59671757
|
GTATATGT others(29): Show |
G | 1 | a0002c0002t0003g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-31+16587_-31+1662 others(40): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671757 | |||||
| chr12:59671762
|
T | A | 1 | a0001c0001t0009g0243 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-31+16512T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671762 | ||||||
| chr12:59671767
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-31+16517A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671767 | ||||||
| chr12:59671809
|
G | A | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+16559G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671809 | ||||||
| chr12:59671809
|
GTA | G | 8 | a0001c0001t0002g0071a0001c0001t0006g0117a0001c0001t0006g0159others(5): Show | 8 | HG00140.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+16567_-31+1656 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671809 | |||||
| chr12:59671835
|
G | A | 1 | a0001c0001t0037g0154 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-31+16585G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671835 | ||||||
| chr12:59671849
|
A | ATATGTG | 3 | a0001c0001t0041g0232a0001c0001t0043g0047a0002c0002t0003g0076 | 3 | HG02630.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-31+16602_-31+1660 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671849 | |||||
| chr12:59671857
|
G | A | 4 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16607G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671857 | ||||||
| chr12:59671857
|
G | GTATATGT others(1): Show |
75 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-31+16615_-31+1662 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671857 | |||||
| chr12:59671873
|
G | A | 3 | a0001c0001t0006g0253a0001c0001t0046g0002a0002c0002t0008g0206 | 3 | HG02559.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-31+16623G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671873 | ||||||
| chr12:59671879
|
A | G | 4 | a0001c0001t0006g0253a0001c0001t0046g0002a0002c0002t0003g0106others(1): Show | 4 | HG02080.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16629A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671879 | ||||||
| chr12:59671883
|
A | G | 14 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(11): Show | 14 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+16633A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671883 | ||||||
| chr12:59671890
|
TACATATG others(9): Show |
T | 1 | a0002c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+16642_-31+1665 others(20): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671890 | |||||
| chr12:59671891
|
A | G | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+16641A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671891 | ||||||
| chr12:59671892
|
C | T | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+16642C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671892 | ||||||
| chr12:59671901
|
A | G | 18 | a0001c0001t0001g0113a0001c0001t0006g0117a0001c0001t0006g0159others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31+16651A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671901 | ||||||
| chr12:59671906
|
C | T | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+16656C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671906 | ||||||
| chr12:59671911
|
A | G | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+16661A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671911 | ||||||
| chr12:59671916
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150others(4): Show | 7 | HG00673.hp2 HG03486.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+16666T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671916 | ||||||
| chr12:59671921
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-31+16671G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671921 | ||||||
| chr12:59671921
|
GTATATAT others(7): Show |
G | 2 | a0002c0002t0003g0008a0002c0002t0003g0228 | 2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-31+16673_-31+1668 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671921 | |||||
| chr12:59671922
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-31+16672T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671922 | ||||||
| chr12:59671923
|
A | ATATATG | 5 | a0001c0001t0002g0101a0001c0001t0013g0259a0001c0001t0015g0258others(2): Show | 5 | HG02451.hp2 HG02735.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16678_-31+1667 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671923 | |||||
| chr12:59671928
|
TCC | T | 16 | a0001c0001t0002g0119a0001c0001t0002g0160a0001c0001t0002g0161others(13): Show | 16 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+16679_-31+1668 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671928 | ||||||
| chr12:59671929
|
C | A | 143 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-31+16679C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671929 | ||||||
| chr12:59671929
|
C | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 98 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-31+16679C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671929 | ||||||
| chr12:59671930
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-31+16680C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671930 | ||||||
| chr12:59671931
|
A | G | 16 | a0001c0001t0002g0119a0001c0001t0002g0160a0001c0001t0002g0161others(13): Show | 16 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+16681A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671931 | ||||||
| chr12:59671932
|
T | C | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+16682T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671932 | ||||||
| chr12:59671935
|
A | ATG | 8 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+16687_-31+1668 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671935 | |||||
| chr12:59671939
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-31+16689A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671939 | ||||||
| chr12:59671940
|
T | C | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16690T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671940 | ||||||
| chr12:59671943
|
ATG | A | 4 | a0001c0001t0006g0253a0001c0001t0046g0002a0002c0002t0003g0008others(1): Show | 4 | HG01496.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16697_-31+1669 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671943 | |||||
| chr12:59671944
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31+16694T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671944 | ||||||
| chr12:59671945
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+16695G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671945 | ||||||
| chr12:59671945
|
G | GTATATAT others(7): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150others(2): Show | 5 | HG00673.hp2 NA18947.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16696_-31+1669 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671945 | |||||
| chr12:59671945
|
G | GTATATAT others(31): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0067 | 2 | NA18951.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-31+16696_-31+1669 others(42): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671945 | |||||
| chr12:59671945
|
G | GTGTATAT others(1): Show |
73 | a0001c0001t0001g0155a0001c0001t0001g0194a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-31+16707_-31+1671 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671945 | |||||
| chr12:59671945
|
G | GTGTATAT others(27): Show |
5 | a0001c0001t0007g0097a0001c0001t0007g0158a0001c0001t0007g0168others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16714_-31+1671 others(38): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671945 | |||||
| chr12:59671945
|
GTGTATAT others(1): Show |
G | 4 | a0001c0001t0048g0081a0002c0002t0003g0085a0002c0002t0008g0072others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16707_-31+1671 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671945 | |||||
| chr12:59671946
|
T | C | 9 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(6): Show | 9 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+16696T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671946 | ||||||
| chr12:59671947
|
G | A | 45 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0026others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.-31+16697G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671947 | ||||||
| chr12:59671948
|
T | C | 4 | a0001c0001t0006g0253a0001c0001t0019g0080a0001c0001t0046g0002others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16698T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671948 | ||||||
| chr12:59671948
|
T | TATATAC | 4 | a0001c0001t0002g0140a0001c0001t0002g0224a0001c0003t0005g0074others(1): Show | 4 | HG01884.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+16703_-31+1670 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671948 | |||||
| chr12:59671948
|
T | TATATACA others(23): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0006g0029 | 3 | HG02486.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-31+16703_-31+1670 others(34): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671948 | |||||
| chr12:59671948
|
T | TATATACA others(47): Show |
1 | a0001c0001t0011g0024 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-31+16703_-31+1670 others(58): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671948 | |||||
| chr12:59671950
|
T | TATAC | 21 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0032others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+16703_-31+1670 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671950 | |||||
| chr12:59671953
|
A | ACATATAT others(57): Show |
1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-31+16703_-31+1670 others(68): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671953 | ||||||
| chr12:59671953
|
A | ACATATAT others(57): Show |
1 | a0001c0001t0015g0004 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-31+16703_-31+1670 others(68): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671953 | ||||||
| chr12:59671953
|
ATGTATAT others(3): Show |
A | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31+16713_-31+1672 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671953 | |||||
| chr12:59671954
|
T | C | 9 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(6): Show | 9 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+16704T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671954 | ||||||
| chr12:59671954
|
TGTATATA others(99): Show |
T | 5 | a0001c0001t0006g0171a0001c0001t0006g0226a0002c0002t0008g0206others(2): Show | 5 | HG02109.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16706_-31+1681 others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671954 | |||||
| chr12:59671955
|
G | A | 23 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.-31+16705G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671955 | ||||||
| chr12:59671956
|
T | C | 1 | a0001c0001t0019g0080 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+16706T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671956 | ||||||
| chr12:59671957
|
A | ATATATG | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+16709_-31+1671 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671957 | |||||
| chr12:59671957
|
A | G | 22 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0032others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+16707A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671957 | ||||||
| chr12:59671958
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-31+16708T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671958 | ||||||
| chr12:59671958
|
T | TATATAC | 7 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0067others(4): Show | 7 | HG00673.hp2 NA18947.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+16712_-31+1671 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671958 | |||||
| chr12:59671959
|
ATATGTGT others(105): Show |
A | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+16713_-31+1682 others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671959 | |||||
| chr12:59671963
|
G | A | 43 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-31+16713G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671963 | ||||||
| chr12:59671963
|
G | GTATATAT others(15): Show |
2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+16714_-31+1671 others(26): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671963 | |||||
| chr12:59671963
|
G | GTATATAT others(39): Show |
1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+16714_-31+1671 others(50): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671963 | |||||
| chr12:59671963
|
GTGTATAT others(15): Show |
G | 16 | a0001c0001t0002g0119a0001c0001t0002g0160a0001c0001t0002g0161others(13): Show | 16 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31+16715_-31+1673 others(26): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671963 | |||||
| chr12:59671964
|
T | C | 4 | a0001c0001t0009g0243a0001c0001t0042g0252a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+16714T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671964 | ||||||
| chr12:59671965
|
G | A | 6 | a0001c0001t0002g0140a0001c0001t0009g0243a0001c0001t0025g0248others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+16715G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671965 | ||||||
| chr12:59671966
|
T | C | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-31+16716T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671966 | ||||||
| chr12:59671968
|
T | TATAC | 7 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0002g0140others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+16721_-31+1672 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671968 | |||||
| chr12:59671970
|
TATCCATA others(54): Show |
T | 4 | a0001c0001t0009g0243a0001c0001t0042g0252a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+16721_-31+1678 others(65): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671970 | ||||||
| chr12:59671972
|
TCCATATA others(3): Show |
T | 1 | a0001c0001t0001g0027 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-31+16723_-31+1673 others(14): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671972 | ||||||
| chr12:59671973
|
C | A | 223 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-31+16723C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671973 | ||||||
| chr12:59671973
|
C | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0067others(6): Show | 9 | HG00673.hp2 HG02615.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+16723C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671973 | ||||||
| chr12:59671974
|
C | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0025others(13): Show | 16 | HG00673.hp2 HG02486.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+16724C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671974 | ||||||
| chr12:59671975
|
A | ATATATG | 3 | a0001c0001t0002g0224a0001c0003t0005g0074a0001c0003t0005g0075 | 3 | HG01884.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+16730_-31+1673 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671975 | |||||
| chr12:59671975
|
A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0002g0140others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+16725A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671975 | ||||||
| chr12:59671980
|
TCC | T | 3 | a0001c0001t0025g0248a0001c0001t0031g0010a0001c0001t0045g0013 | 3 | HG01169.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-31+16731_-31+1673 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671980 | ||||||
| chr12:59671981
|
C | A | 208 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-31+16731C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671981 | ||||||
| chr12:59671981
|
C | G | 19 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0032others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-31+16731C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671981 | ||||||
| chr12:59671982
|
C | T | 28 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0026others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-31+16732C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671982 | ||||||
| chr12:59671983
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16733G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671983 | ||||||
| chr12:59671985
|
A | ATATG | 5 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150others(2): Show | 5 | HG00673.hp2 NA18947.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16738_-31+1673 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671985 | |||||
| chr12:59671985
|
A | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0030others(12): Show | 15 | HG01261.hp1 HG01884.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31+16735A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671985 | ||||||
| chr12:59671987
|
A | ATATGTAT others(29): Show |
1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-31+16740_-31+1674 others(40): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671987 | |||||
| chr12:59671987
|
A | ATG | 21 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+16738_-31+1673 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671987 | |||||
| chr12:59671991
|
A | G | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16741A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671991 | ||||||
| chr12:59671993
|
G | A | 22 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+16743G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671993 | ||||||
| chr12:59671995
|
G | A | 20 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0032others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+16745G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671995 | ||||||
| chr12:59671996
|
T | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+16746T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671996 | ||||||
| chr12:59671996
|
T | TATATAC | 5 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150others(2): Show | 5 | HG00673.hp2 NA18947.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16751_-31+1675 others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59671996 | |||||
| chr12:59671997
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-31+16747A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59671997 | ||||||
| chr12:59672001
|
A | G | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16751A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672001 | ||||||
| chr12:59672003
|
C | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(215): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-31+16753C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672003 | ||||||
| chr12:59672003
|
C | G | 31 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.-31+16753C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672003 | ||||||
| chr12:59672004
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16754C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672004 | ||||||
| chr12:59672010
|
TCC | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0031g0010 | 3 | HG01169.hp2 NA18951.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-31+16761_-31+1676 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672010 | ||||||
| chr12:59672011
|
C | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-31+16761C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672011 | ||||||
| chr12:59672011
|
C | G | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.-31+16761C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672011 | ||||||
| chr12:59672012
|
C | CGT | 10 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0030others(7): Show | 10 | HG01261.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+16763_-31+1676 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672012 | |||||
| chr12:59672012
|
C | T | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.-31+16762C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672012 | ||||||
| chr12:59672013
|
G | A | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16763G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672013 | ||||||
| chr12:59672013
|
G | GTA | 21 | a0001c0001t0002g0119a0001c0001t0002g0160a0001c0001t0002g0161others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+16769_-31+1677 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672013 | |||||
| chr12:59672013
|
GTATATAT others(84): Show |
G | 4 | a0001c0001t0048g0081a0002c0002t0003g0085a0002c0002t0008g0072others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+16781_-31+1687 others(95): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672013 | |||||
| chr12:59672020
|
T | C | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16770T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672020 | ||||||
| chr12:59672022
|
TGTATATA others(4): Show |
T | 1 | a0002c0002t0024g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31+16773_-31+1678 others(15): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672022 | ||||||
| chr12:59672023
|
G | A | 1 | a0001c0001t0045g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-31+16773G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672023 | ||||||
| chr12:59672030
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-31+16780T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672030 | ||||||
| chr12:59672030
|
TC | T | 176 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-31+16781delC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672030 | ||||||
| chr12:59672030
|
TCGCATAT others(23): Show |
T | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-31+16781_-31+1681 others(34): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672030 | ||||||
| chr12:59672030
|
TCGCATAT others(54): Show |
T | 63 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-31+16781_-31+1684 others(65): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672030 | ||||||
| chr12:59672031
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0067 | 2 | NA18951.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-31+16781C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672031 | ||||||
| chr12:59672032
|
G | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-31+16782G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672032 | ||||||
| chr12:59672033
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0009g0243a0001c0001t0042g0252others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+16783C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672033 | ||||||
| chr12:59672039
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-31+16789T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672039 | ||||||
| chr12:59672040
|
C | A | 178 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-31+16790C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672040 | ||||||
| chr12:59672040
|
C | G | 7 | a0001c0001t0001g0067a0001c0001t0009g0243a0001c0001t0042g0252others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+16790C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672040 | ||||||
| chr12:59672041
|
C | CGT | 35 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-31+16792_-31+1679 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672041 | |||||
| chr12:59672041
|
C | T | 7 | a0001c0001t0001g0067a0001c0001t0009g0243a0001c0001t0042g0252others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+16791C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672041 | ||||||
| chr12:59672042
|
G | GTA | 28 | a0001c0001t0001g0208a0001c0001t0002g0057a0001c0001t0002g0086others(25): Show | 28 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-31+16798_-31+1679 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672042 | |||||
| chr12:59672042
|
G | GTATATAT others(25): Show |
9 | a0001c0001t0009g0244a0001c0001t0012g0166a0001c0001t0012g0246others(6): Show | 9 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+16799_-31+1680 others(36): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672042 | |||||
| chr12:59672042
|
G | GTATATAT others(55): Show |
1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-31+16799_-31+1680 others(66): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672042 | |||||
| chr12:59672042
|
GTATATAT others(55): Show |
G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-31+16810_-31+1687 others(66): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672042 | |||||
| chr12:59672059
|
T | TGCATATA others(38): Show |
1 | a0002c0002t0004g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-31+16809_-31+1681 others(49): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672059 | ||||||
| chr12:59672059
|
T | TGCATATA others(66): Show |
1 | a0002c0002t0023g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-31+16809_-31+1681 others(77): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672059 | ||||||
| chr12:59672059
|
TC | T | 182 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-31+16810delC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672059 | ||||||
| chr12:59672060
|
C | T | 2 | a0002c0002t0004g0256a0002c0002t0023g0238 | 2 | HG00099.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-31+16810C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672060 | ||||||
| chr12:59672061
|
G | A | 49 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-31+16811G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672061 | ||||||
| chr12:59672069
|
C | A | 190 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-31+16819C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672069 | ||||||
| chr12:59672071
|
GTA | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0002g0140others(8): Show | 11 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+16829_-31+1683 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672071 | |||||
| chr12:59672071
|
GTATATAT others(26): Show |
G | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-31+16829_-31+1686 others(37): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672071 | |||||
| chr12:59672073
|
A | G | 29 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-31+16823A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672073 | ||||||
| chr12:59672076
|
T | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+16826T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672076 | ||||||
| chr12:59672081
|
G | A | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+16831G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672081 | ||||||
| chr12:59672090
|
T | TGCATATA others(22): Show |
2 | a0001c0001t0002g0132a0001c0001t0007g0139 | 2 | HG03710.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-31+16840_-31+1684 others(33): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672090 | ||||||
| chr12:59672090
|
TC | T | 187 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-31+16841delC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672090 | ||||||
| chr12:59672090
|
TCGCATAT others(4): Show |
T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+16841_-31+1685 others(15): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672090 | ||||||
| chr12:59672091
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0007g0139 | 2 | HG03710.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-31+16841C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672091 | ||||||
| chr12:59672092
|
G | A | 29 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.-31+16842G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672092 | ||||||
| chr12:59672100
|
C | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-31+16850C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672100 | ||||||
| chr12:59672102
|
GTA | G | 39 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-31+16860_-31+1686 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672102 | |||||
| chr12:59672104
|
A | G | 2 | a0001c0001t0001g0067a0002c0002t0003g0076 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-31+16854A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672104 | ||||||
| chr12:59672106
|
A | G | 1 | a0001c0001t0014g0211 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-31+16856A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672106 | ||||||
| chr12:59672110
|
ATGTGTAT others(5): Show |
A | 1 | a0001c0001t0030g0018 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-31+16861_-31+1687 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672110 | ||||||
| chr12:59672112
|
G | A | 2 | a0001c0001t0006g0225a0001c0001t0018g0005 | 2 | HG02486.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-31+16862G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672112 | ||||||
| chr12:59672113
|
T | C | 5 | a0001c0001t0006g0225a0001c0001t0018g0005a0001c0001t0020g0006others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+16863T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672113 | ||||||
| chr12:59672122
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0014g0145others(2): Show | 5 | HG02155.hp2 HG02922.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+16872G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672122 | ||||||
| chr12:59672131
|
CGT | C | 7 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0045g0013others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+16882_-31+1688 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672131 | ||||||
| chr12:59672134
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0067a0001c0001t0025g0248 | 3 | HG02615.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-31+16884A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672134 | ||||||
| chr12:59672140
|
ATG | A | 21 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(18): Show | 21 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+16894_-31+1689 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672140 | |||||
| chr12:59672140
|
ATGTGTAT others(5): Show |
A | 10 | a0001c0001t0001g0208a0001c0001t0002g0057a0001c0001t0002g0086others(7): Show | 10 | HG02155.hp1 HG02615.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+16891_-31+1690 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672140 | ||||||
| chr12:59672143
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+16893T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672143 | ||||||
| chr12:59672162
|
GTA | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0118a0001c0001t0013g0069others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+16920_-31+1692 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672162 | |||||
| chr12:59672171
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16921T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672171 | ||||||
| chr12:59672172
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-31+16922G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672172 | ||||||
| chr12:59672172
|
GTGTATAT others(11): Show |
G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+16923_-31+1694 others(22): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672172 | ||||||
| chr12:59672173
|
T | C | 19 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(16): Show | 19 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.-31+16923T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672173 | ||||||
| chr12:59672174
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16924G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672174 | ||||||
| chr12:59672179
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16929T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672179 | ||||||
| chr12:59672180
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16930A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672180 | ||||||
| chr12:59672182
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16932G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672182 | ||||||
| chr12:59672182
|
GCATATAT others(11): Show |
G | 9 | a0001c0001t0001g0208a0001c0001t0002g0057a0001c0001t0002g0086others(6): Show | 9 | HG02155.hp1 NA18944.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+16951_-31+1696 others(22): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672182 | |||||
| chr12:59672183
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16933C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672183 | ||||||
| chr12:59672190
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16940A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672190 | ||||||
| chr12:59672191
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-31+16941C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672191 | ||||||
| chr12:59672191
|
CGTATATA others(9): Show |
C | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-31+16942_-31+1695 others(20): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672191 | ||||||
| chr12:59672192
|
GTATATAT others(13): Show |
G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+16950_-31+1696 others(24): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672192 | |||||
| chr12:59672194
|
A | G | 4 | a0001c0001t0009g0243a0001c0001t0042g0252a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+16944A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672194 | ||||||
| chr12:59672200
|
A | ATG | 3 | a0001c0001t0002g0058a0001c0001t0002g0118a0001c0001t0025g0248 | 3 | HG02109.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+16950_-31+1695 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672200 | ||||||
| chr12:59672200
|
A | ATGTGTAT others(5): Show |
3 | a0001c0001t0001g0044a0001c0001t0034g0084a0002c0002t0004g0040 | 3 | HG00099.hp2 HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-31+16950_-31+1695 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672200 | ||||||
| chr12:59672200
|
A | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(65): Show | 68 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-31+16950A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672200 | ||||||
| chr12:59672201
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(24): Show | 27 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16951C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672201 | ||||||
| chr12:59672202
|
A | G | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(24): Show | 27 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16952A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672202 | ||||||
| chr12:59672204
|
A | G | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16954A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672204 | ||||||
| chr12:59672209
|
C | T | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(24): Show | 27 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16959C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672209 | ||||||
| chr12:59672210
|
G | A | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(24): Show | 27 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16960G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672210 | ||||||
| chr12:59672211
|
T | C | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-31+16961T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672211 | ||||||
| chr12:59672212
|
A | G | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16962A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672212 | ||||||
| chr12:59672213
|
T | C | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16963T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672213 | ||||||
| chr12:59672219
|
T | C | 2 | a0001c0001t0025g0248a0001c0003t0005g0195 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-31+16969T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672219 | ||||||
| chr12:59672220
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16970G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672220 | ||||||
| chr12:59672221
|
T | C | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(24): Show | 27 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+16971T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672221 | ||||||
| chr12:59672222
|
G | A | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-31+16972G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672222 | ||||||
| chr12:59672230
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(23): Show | 26 | HG00673.hp2 HG01123.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-31+16980G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672230 | ||||||
| chr12:59672230
|
G | GCATATAT others(11): Show |
3 | a0001c0001t0001g0044a0001c0001t0034g0084a0002c0002t0004g0040 | 3 | HG00099.hp2 HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-31+16981_-31+1699 others(22): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672230 | |||||
| chr12:59672239
|
C | T | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-31+16989C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672239 | ||||||
| chr12:59672250
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+17000G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672250 | ||||||
| chr12:59672251
|
T | C | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+17001T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672251 | ||||||
| chr12:59672254
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+17004A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672254 | ||||||
| chr12:59672269
|
CGTATATA others(5): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-31+17042_-31+1705 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59672269 | |||||
| chr12:59672272
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-31+17022A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672272 | ||||||
| chr12:59672323
|
C | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+17073C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672323 | ||||||
| chr12:59672432
|
C | T | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+17182C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672432 | ||||||
| chr12:59672460
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-31+17210C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672460 | ||||||
| chr12:59672516
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+17266C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672516 | ||||||
| chr12:59672632
|
T | C | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+17382T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672632 | ||||||
| chr12:59672684
|
T | A | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-31+17434T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672684 | ||||||
| chr12:59672696
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+17446G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672696 | ||||||
| chr12:59672990
|
A | G | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31+17740A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59672990 | ||||||
| chr12:59673084
|
A | G | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31+17834A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59673084 | ||||||
| chr12:59673093
|
G | A | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+17843G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59673093 | ||||||
| chr12:59673280
|
C | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-31+18030C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59673280 | ||||||
| chr12:59673284
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+18034A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59673284 | ||||||
| chr12:59673411
|
C | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+18161C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59673411 | ||||||
| chr12:59673482
|
G | GT | 39 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.-31+18246dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59673482 | |||||
| chr12:59674051
|
G | A | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+18801G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59674051 | ||||||
| chr12:59674524
|
C | T | 1 | a0001c0001t0011g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-31+19274C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59674524 | ||||||
| chr12:59674570
|
T | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+19320T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59674570 | ||||||
| chr12:59674575
|
G | A | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+19325G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59674575 | ||||||
| chr12:59674955
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+19705C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59674955 | ||||||
| chr12:59675018
|
C | T | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-31+19768C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675018 | ||||||
| chr12:59675021
|
G | A | 2 | a0002c0002t0003g0085a0002c0002t0008g0088 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-31+19771G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675021 | ||||||
| chr12:59675056
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-31+19806G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675056 | ||||||
| chr12:59675057
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-31+19807T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675057 | ||||||
| chr12:59675174
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00639.hp1 HG00738.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-31+19924C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675174 | ||||||
| chr12:59675492
|
GA | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-31+20249delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59675492 | |||||
| chr12:59675547
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+20297G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675547 | ||||||
| chr12:59675573
|
A | T | 8 | a0001c0001t0006g0171a0001c0001t0006g0226a0001c0001t0045g0013others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+20323A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675573 | ||||||
| chr12:59675661
|
T | C | 1 | a0001c0001t0018g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-31+20411T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675661 | ||||||
| chr12:59675698
|
T | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+20448T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675698 | ||||||
| chr12:59675761
|
A | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-31+20511A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59675761 | ||||||
| chr12:59676048
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+20798G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676048 | ||||||
| chr12:59676050
|
G | A | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+20800G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676050 | ||||||
| chr12:59676141
|
A | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+20891A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676141 | ||||||
| chr12:59676247
|
A | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+20997A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676247 | ||||||
| chr12:59676360
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-31+21110A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676360 | ||||||
| chr12:59676424
|
C | T | 3 | a0001c0001t0002g0065a0001c0001t0011g0178a0001c0001t0035g0066 | 3 | HG00673.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-31+21174C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676424 | ||||||
| chr12:59676430
|
AT | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21189delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59676430 | |||||
| chr12:59676613
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31+21363G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676613 | ||||||
| chr12:59676637
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-31+21387C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676637 | ||||||
| chr12:59676679
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21429T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676679 | ||||||
| chr12:59676727
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21477A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676727 | ||||||
| chr12:59676830
|
C | T | 53 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.-31+21580C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676830 | ||||||
| chr12:59676837
|
TA | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21592delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59676837 | |||||
| chr12:59676941
|
C | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21691C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59676941 | ||||||
| chr12:59677052
|
C | T | 1 | a0001c0001t0035g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-31+21802C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677052 | ||||||
| chr12:59677063
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+21813A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677063 | ||||||
| chr12:59677150
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-31+21900G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677150 | ||||||
| chr12:59677323
|
G | T | 1 | a0001c0003t0005g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-31+22073G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677323 | ||||||
| chr12:59677687
|
A | G | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-31+22437A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677687 | ||||||
| chr12:59677787
|
G | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+22537G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677787 | ||||||
| chr12:59677842
|
T | A | 2 | a0001c0001t0041g0232a0001c0001t0043g0047 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-31+22592T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677842 | ||||||
| chr12:59677850
|
T | A | 1 | a0001c0001t0006g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-31+22600T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677850 | ||||||
| chr12:59677889
|
C | G | 10 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(7): Show | 10 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31+22639C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677889 | ||||||
| chr12:59677958
|
C | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31+22708C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677958 | ||||||
| chr12:59677968
|
G | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(173): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-31+22718G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59677968 | ||||||
| chr12:59678174
|
C | T | 24 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(21): Show | 24 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.-31+22924C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678174 | ||||||
| chr12:59678178
|
G | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+22928G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678178 | ||||||
| chr12:59678424
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23174G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678424 | ||||||
| chr12:59678440
|
TTAGCAGA others(5): Show |
T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23193_-31+2320 others(16): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59678440 | |||||
| chr12:59678480
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+23230C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678480 | ||||||
| chr12:59678568
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23318G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678568 | ||||||
| chr12:59678645
|
C | A | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31+23395C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678645 | ||||||
| chr12:59678652
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23402G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678652 | ||||||
| chr12:59678653
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23403G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678653 | ||||||
| chr12:59678767
|
C | G | 3 | a0001c0001t0011g0054a0001c0001t0027g0090a0002c0002t0004g0092 | 3 | NA18747.hp1 NA18951.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-31+23517C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678767 | ||||||
| chr12:59678776
|
C | G | 1 | a0002c0002t0017g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-31+23526C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678776 | ||||||
| chr12:59678791
|
T | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-31+23541T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678791 | ||||||
| chr12:59678914
|
G | T | 1 | a0001c0001t0018g0005 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-31+23664G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59678914 | ||||||
| chr12:59679132
|
A | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23882A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679132 | ||||||
| chr12:59679133
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23883G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679133 | ||||||
| chr12:59679192
|
A | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+23942A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679192 | ||||||
| chr12:59679213
|
C | A | 2 | a0001c0001t0006g0253a0001c0001t0046g0002 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-31+23963C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679213 | ||||||
| chr12:59679220
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-31+23970C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679220 | ||||||
| chr12:59679301
|
C | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24051C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679301 | ||||||
| chr12:59679332
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24082G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679332 | ||||||
| chr12:59679429
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-31+24179C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679429 | ||||||
| chr12:59679459
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24209A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679459 | ||||||
| chr12:59679707
|
A | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24457A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679707 | ||||||
| chr12:59679741
|
C | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24491C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679741 | ||||||
| chr12:59679817
|
A | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+24567A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59679817 | ||||||
| chr12:59680008
|
G | A | 79 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-31+24758G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680008 | ||||||
| chr12:59680064
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30-24708C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680064 | ||||||
| chr12:59680126
|
C | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-24646C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680126 | ||||||
| chr12:59680241
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-24531A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680241 | ||||||
| chr12:59680274
|
C | G | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-30-24498C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680274 | ||||||
| chr12:59680299
|
A | C | 2 | a0002c0002t0017g0182a0007c0008t0040g0151 | 2 | HG00609.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-30-24473A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680299 | ||||||
| chr12:59680318
|
A | G | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-30-24454A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680318 | ||||||
| chr12:59680404
|
G | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-30-24368G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680404 | ||||||
| chr12:59680518
|
C | T | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-24254C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680518 | ||||||
| chr12:59680593
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-30-24179T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680593 | ||||||
| chr12:59680777
|
G | T | 3 | a0001c0001t0006g0001a0001c0001t0041g0232a0001c0001t0043g0047 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-30-23995G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680777 | ||||||
| chr12:59680825
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-23947G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59680825 | ||||||
| chr12:59681212
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-30-23560A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681212 | ||||||
| chr12:59681253
|
A | G | 1 | a0002c0002t0004g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-30-23519A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681253 | ||||||
| chr12:59681449
|
A | AT | 21 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(18): Show | 21 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30-23312dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59681449 | |||||
| chr12:59681486
|
C | A | 1 | a0002c0002t0004g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-30-23286C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681486 | ||||||
| chr12:59681522
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-23250G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681522 | ||||||
| chr12:59681554
|
T | C | 5 | a0001c0001t0009g0243a0001c0001t0025g0248a0001c0001t0042g0252others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-23218T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681554 | ||||||
| chr12:59681583
|
C | T | 1 | a0004c0005t0009g0089 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-30-23189C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681583 | ||||||
| chr12:59681602
|
A | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-23170A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681602 | ||||||
| chr12:59681890
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0009g0243a0001c0001t0025g0248others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-22882A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681890 | ||||||
| chr12:59681951
|
CAT | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-22819_-30-2281 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59681951 | |||||
| chr12:59681956
|
C | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-22816C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59681956 | ||||||
| chr12:59682074
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-30-22698T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682074 | ||||||
| chr12:59682305
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-22467A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682305 | ||||||
| chr12:59682457
|
A | T | 4 | a0001c0001t0009g0243a0001c0001t0025g0248a0003c0004t0009g0249others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-22315A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682457 | ||||||
| chr12:59682600
|
G | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-22172G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682600 | ||||||
| chr12:59682671
|
A | C | 1 | a0001c0001t0030g0018 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-30-22101A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682671 | ||||||
| chr12:59682788
|
C | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG00735.hp2 HG01358.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-21984C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682788 | ||||||
| chr12:59682792
|
C | T | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30-21980C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682792 | ||||||
| chr12:59682887
|
G | A | 13 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(10): Show | 13 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30-21885G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682887 | ||||||
| chr12:59682927
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21845G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682927 | ||||||
| chr12:59682981
|
A | C | 1 | a0001c0001t0006g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30-21791A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59682981 | ||||||
| chr12:59683007
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30-21765G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683007 | ||||||
| chr12:59683053
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21719T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683053 | ||||||
| chr12:59683067
|
GA | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21695delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59683067 | |||||
| chr12:59683192
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-30-21580G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683192 | ||||||
| chr12:59683195
|
T | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21577T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683195 | ||||||
| chr12:59683246
|
T | C | 3 | a0001c0001t0002g0146a0001c0001t0002g0173a0001c0001t0002g0197 | 3 | HG00280.hp2 HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-30-21526T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683246 | ||||||
| chr12:59683323
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21449T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683323 | ||||||
| chr12:59683351
|
G | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21421G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683351 | ||||||
| chr12:59683423
|
A | G | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21349A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683423 | ||||||
| chr12:59683434
|
A | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21338A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683434 | ||||||
| chr12:59683562
|
A | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21210A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683562 | ||||||
| chr12:59683575
|
C | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21197C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683575 | ||||||
| chr12:59683601
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0032others(2): Show | 5 | HG01928.hp2 HG02148.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-21171A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683601 | ||||||
| chr12:59683709
|
T | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-21063T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683709 | ||||||
| chr12:59683819
|
T | C | 1 | a0001c0003t0005g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-30-20953T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59683819 | ||||||
| chr12:59684055
|
A | G | 1 | a0002c0002t0003g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-30-20717A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684055 | ||||||
| chr12:59684086
|
C | T | 1 | a0001c0003t0005g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-30-20686C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684086 | ||||||
| chr12:59684125
|
G | A | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-20647G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684125 | ||||||
| chr12:59684172
|
T | A | 2 | a0001c0001t0041g0232a0001c0001t0043g0047 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-30-20600T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684172 | ||||||
| chr12:59684178
|
C | T | 3 | a0001c0001t0013g0259a0001c0001t0015g0258a0001c0001t0020g0006 | 3 | HG02451.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-20594C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684178 | ||||||
| chr12:59684207
|
A | G | 19 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(16): Show | 19 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30-20565A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684207 | ||||||
| chr12:59684244
|
A | T | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30-20528A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684244 | ||||||
| chr12:59684254
|
A | T | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-20518A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684254 | ||||||
| chr12:59684321
|
T | C | 22 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(19): Show | 22 | HG00597.hp2 HG01175.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-20451T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684321 | ||||||
| chr12:59684732
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-30-20040A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59684732 | ||||||
| chr12:59685049
|
G | A | 47 | a0001c0001t0001g0043a0001c0001t0002g0051a0001c0001t0002g0213others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30-19723G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685049 | ||||||
| chr12:59685052
|
T | C | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30-19720T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685052 | ||||||
| chr12:59685095
|
G | T | 12 | a0001c0001t0006g0029a0001c0001t0006g0117a0001c0001t0006g0159others(9): Show | 12 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-30-19677G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685095 | ||||||
| chr12:59685110
|
C | T | 14 | a0001c0001t0006g0029a0001c0001t0006g0117a0001c0001t0006g0159others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-19662C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685110 | ||||||
| chr12:59685115
|
A | G | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-19657A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685115 | ||||||
| chr12:59685294
|
A | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(47): Show | 50 | HG00099.hp2 HG00673.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-30-19478A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685294 | ||||||
| chr12:59685298
|
T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(47): Show | 50 | HG00099.hp2 HG00673.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-30-19474T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685298 | ||||||
| chr12:59685301
|
G | A | 2 | a0001c0001t0006g0253a0001c0001t0045g0013 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-30-19471G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685301 | ||||||
| chr12:59685364
|
C | T | 1 | a0001c0001t0006g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-30-19408C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685364 | ||||||
| chr12:59685365
|
G | A | 1 | a0001c0001t0015g0004 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30-19407G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685365 | ||||||
| chr12:59685594
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-30-19178G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685594 | ||||||
| chr12:59685623
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-30-19149G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685623 | ||||||
| chr12:59685821
|
A | T | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-18951A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685821 | ||||||
| chr12:59685867
|
A | G | 1 | a0001c0001t0007g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-30-18905A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685867 | ||||||
| chr12:59685885
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-18887T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685885 | ||||||
| chr12:59685996
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-18776A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59685996 | ||||||
| chr12:59686071
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-18701G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686071 | ||||||
| chr12:59686074
|
A | G | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-30-18698A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686074 | ||||||
| chr12:59686095
|
C | CT | 59 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 59 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-30-18656dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59686095 | |||||
| chr12:59686095
|
CT | C | 14 | a0001c0001t0013g0069a0001c0001t0013g0259a0002c0002t0003g0076others(11): Show | 14 | HG00558.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30-18656delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59686095 | |||||
| chr12:59686095
|
CTT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-30-18657_-30-1865 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59686095 | |||||
| chr12:59686126
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-18646G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686126 | ||||||
| chr12:59686202
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-30-18570T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686202 | ||||||
| chr12:59686362
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-18410A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686362 | ||||||
| chr12:59686583
|
A | G | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-30-18189A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686583 | ||||||
| chr12:59686753
|
C | T | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-30-18019C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686753 | ||||||
| chr12:59686804
|
A | G | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-17968A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686804 | ||||||
| chr12:59686961
|
A | C | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-17811A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686961 | ||||||
| chr12:59686973
|
A | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-30-17799A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59686973 | ||||||
| chr12:59687089
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-17683C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687089 | ||||||
| chr12:59687110
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-30-17662C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687110 | ||||||
| chr12:59687218
|
G | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-17554G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687218 | ||||||
| chr12:59687249
|
C | T | 17 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30-17523C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687249 | ||||||
| chr12:59687289
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-17483T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687289 | ||||||
| chr12:59687298
|
G | A | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-17474G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687298 | ||||||
| chr12:59687321
|
A | G | 1 | a0001c0003t0005g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-30-17451A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687321 | ||||||
| chr12:59687333
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-17439T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687333 | ||||||
| chr12:59687552
|
T | C | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30-17220T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687552 | ||||||
| chr12:59687630
|
A | G | 1 | a0002c0002t0003g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-30-17142A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687630 | ||||||
| chr12:59687745
|
C | A | 1 | a0001c0003t0010g0019 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-30-17027C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687745 | ||||||
| chr12:59687860
|
T | C | 1 | a0002c0002t0003g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-30-16912T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687860 | ||||||
| chr12:59687870
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-16902C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59687870 | ||||||
| chr12:59688117
|
G | A | 1 | a0001c0001t0044g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-30-16655G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688117 | ||||||
| chr12:59688162
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-16610C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688162 | ||||||
| chr12:59688169
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-16603T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688169 | ||||||
| chr12:59688428
|
A | G | 4 | a0002c0002t0003g0114a0002c0002t0003g0147a0002c0002t0003g0149others(1): Show | 4 | HG00735.hp1 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-16344A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688428 | ||||||
| chr12:59688553
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-16219A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688553 | ||||||
| chr12:59688578
|
G | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30-16194G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688578 | ||||||
| chr12:59688725
|
A | G | 10 | a0001c0001t0009g0243a0001c0001t0013g0069a0001c0001t0013g0073others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-16047A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688725 | ||||||
| chr12:59688800
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-15972G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688800 | ||||||
| chr12:59688924
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-15848G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688924 | ||||||
| chr12:59688947
|
G | A | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-15825G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688947 | ||||||
| chr12:59688955
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-15817T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59688955 | ||||||
| chr12:59689315
|
A | T | 30 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(27): Show | 30 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-30-15457A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689315 | ||||||
| chr12:59689324
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-15448T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689324 | ||||||
| chr12:59689343
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-15429T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689343 | ||||||
| chr12:59689466
|
G | A | 1 | a0001c0003t0005g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-30-15306G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689466 | ||||||
| chr12:59689607
|
A | AT | 27 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30-15159dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59689607 | |||||
| chr12:59689638
|
T | G | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-15134T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689638 | ||||||
| chr12:59689707
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-30-15065C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689707 | ||||||
| chr12:59689776
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14996A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689776 | ||||||
| chr12:59689917
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14855A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59689917 | ||||||
| chr12:59690055
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14717A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690055 | ||||||
| chr12:59690207
|
T | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14565T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690207 | ||||||
| chr12:59690258
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14514G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690258 | ||||||
| chr12:59690284
|
G | A | 1 | a0001c0001t0030g0018 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-30-14488G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690284 | ||||||
| chr12:59690537
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-14235A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690537 | ||||||
| chr12:59690544
|
G | A | 6 | a0001c0001t0025g0248a0001c0001t0042g0252a0003c0004t0009g0249others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-14228G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690544 | ||||||
| chr12:59690676
|
G | T | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-30-14096G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690676 | ||||||
| chr12:59690802
|
A | G | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30-13970A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690802 | ||||||
| chr12:59690951
|
T | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0118 | 3 | HG01257.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-13821T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690951 | ||||||
| chr12:59690986
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-13786C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59690986 | ||||||
| chr12:59691250
|
G | T | 1 | a0002c0002t0003g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30-13522G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691250 | ||||||
| chr12:59691285
|
G | A | 2 | a0001c0001t0006g0253a0001c0001t0045g0013 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-30-13487G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691285 | ||||||
| chr12:59691364
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-13408A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691364 | ||||||
| chr12:59691402
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-13370G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691402 | ||||||
| chr12:59691673
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-30-13099A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691673 | ||||||
| chr12:59691772
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-30-13000C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59691772 | ||||||
| chr12:59692113
|
G | A | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-12659G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692113 | ||||||
| chr12:59692285
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12487G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692285 | ||||||
| chr12:59692301
|
A | G | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-12471A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692301 | ||||||
| chr12:59692345
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12427C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692345 | ||||||
| chr12:59692364
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12408C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692364 | ||||||
| chr12:59692417
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12355G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692417 | ||||||
| chr12:59692425
|
A | G | 29 | a0001c0001t0001g0113a0001c0001t0009g0244a0001c0001t0012g0166others(26): Show | 29 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-30-12347A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692425 | ||||||
| chr12:59692469
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12303G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692469 | ||||||
| chr12:59692603
|
A | G | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-30-12169A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692603 | ||||||
| chr12:59692708
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12064A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59692708 | ||||||
| chr12:59693104
|
C | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30-11668C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693104 | ||||||
| chr12:59693583
|
T | G | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-11189T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693583 | ||||||
| chr12:59693585
|
T | G | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-11187T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693585 | ||||||
| chr12:59693648
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-11124A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693648 | ||||||
| chr12:59693721
|
G | A | 8 | a0001c0001t0001g0113a0001c0001t0012g0166a0001c0001t0012g0246others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-11051G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693721 | ||||||
| chr12:59693791
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-30-10981A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693791 | ||||||
| chr12:59693854
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10918A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693854 | ||||||
| chr12:59693966
|
G | A | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30-10806G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693966 | ||||||
| chr12:59693996
|
A | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30-10776A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59693996 | ||||||
| chr12:59694006
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10766G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694006 | ||||||
| chr12:59694074
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10698A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694074 | ||||||
| chr12:59694166
|
A | G | 5 | a0002c0002t0003g0184a0002c0002t0003g0185a0002c0002t0003g0186others(2): Show | 5 | NA18954.hp2 NA18966.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-10606A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694166 | ||||||
| chr12:59694179
|
C | T | 1 | a0001c0001t0012g0254 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30-10593C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694179 | ||||||
| chr12:59694184
|
G | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30-10588G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694184 | ||||||
| chr12:59694466
|
C | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-30-10306C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694466 | ||||||
| chr12:59694474
|
T | A | 2 | a0001c0001t0002g0011a0002c0002t0003g0156 | 2 | HG00408.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-30-10298T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694474 | ||||||
| chr12:59694482
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10290T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694482 | ||||||
| chr12:59694518
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10254C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694518 | ||||||
| chr12:59694555
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10217T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694555 | ||||||
| chr12:59694600
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-10172A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694600 | ||||||
| chr12:59694795
|
G | T | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-30-9977G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694795 | ||||||
| chr12:59694820
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9952G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694820 | ||||||
| chr12:59694874
|
A | G | 1 | a0001c0001t0006g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-30-9898A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59694874 | ||||||
| chr12:59695119
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9653C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695119 | ||||||
| chr12:59695250
|
A | C | 2 | a0002c0002t0004g0056a0002c0002t0004g0098 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-30-9522A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695250 | ||||||
| chr12:59695335
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9437G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695335 | ||||||
| chr12:59695465
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9307T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695465 | ||||||
| chr12:59695527
|
C | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-30-9245C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695527 | ||||||
| chr12:59695548
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9224A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695548 | ||||||
| chr12:59695701
|
G | T | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-30-9071G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695701 | ||||||
| chr12:59695818
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-30-8954T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695818 | ||||||
| chr12:59695866
|
C | T | 1 | a0001c0003t0010g0019 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-30-8906C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695866 | ||||||
| chr12:59695867
|
G | A | 7 | a0001c0001t0009g0243a0001c0001t0025g0248a0001c0001t0042g0252others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-8905G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59695867 | ||||||
| chr12:59696018
|
G | A | 1 | a0001c0001t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-30-8754G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696018 | ||||||
| chr12:59696024
|
G | A | 27 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30-8748G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696024 | ||||||
| chr12:59696106
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8666G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696106 | ||||||
| chr12:59696133
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8639A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696133 | ||||||
| chr12:59696138
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8634G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696138 | ||||||
| chr12:59696160
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8612C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696160 | ||||||
| chr12:59696168
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8604C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696168 | ||||||
| chr12:59696207
|
T | C | 1 | a0002c0002t0003g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-30-8565T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696207 | ||||||
| chr12:59696214
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8558C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696214 | ||||||
| chr12:59696262
|
C | T | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-8510C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696262 | ||||||
| chr12:59696263
|
G | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-30-8509G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696263 | ||||||
| chr12:59696347
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8425A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696347 | ||||||
| chr12:59696426
|
G | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-30-8346G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696426 | ||||||
| chr12:59696433
|
C | T | 8 | a0001c0001t0001g0113a0001c0001t0012g0166a0001c0001t0012g0246others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-8339C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696433 | ||||||
| chr12:59696517
|
A | G | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-8255A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696517 | ||||||
| chr12:59696616
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8156G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696616 | ||||||
| chr12:59696737
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8035T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696737 | ||||||
| chr12:59696769
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-8003C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696769 | ||||||
| chr12:59696897
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7875T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696897 | ||||||
| chr12:59696971
|
A | G | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30-7801A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59696971 | ||||||
| chr12:59697120
|
T | C | 3 | a0001c0001t0007g0097a0001c0001t0007g0158a0001c0001t0007g0168 | 3 | HG02451.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-30-7652T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697120 | ||||||
| chr12:59697237
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-30-7535G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697237 | ||||||
| chr12:59697303
|
C | T | 2 | a0002c0002t0004g0040a0002c0002t0023g0238 | 2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-30-7469C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697303 | ||||||
| chr12:59697306
|
A | C | 3 | a0001c0001t0011g0024a0001c0001t0011g0144a0001c0001t0027g0090 | 3 | HG02071.hp1 NA18747.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-30-7466A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697306 | ||||||
| chr12:59697358
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7414A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697358 | ||||||
| chr12:59697496
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7276G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697496 | ||||||
| chr12:59697513
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7259A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697513 | ||||||
| chr12:59697658
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7114T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697658 | ||||||
| chr12:59697696
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7076C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697696 | ||||||
| chr12:59697738
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-7034A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697738 | ||||||
| chr12:59697857
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-6915G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697857 | ||||||
| chr12:59697879
|
T | G | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-6893T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697879 | ||||||
| chr12:59697984
|
A | G | 2 | a0001c0003t0005g0235a0001c0003t0005g0236 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-30-6788A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59697984 | ||||||
| chr12:59698378
|
A | G | 1 | a0004c0005t0009g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-30-6394A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698378 | ||||||
| chr12:59698423
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-6349T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698423 | ||||||
| chr12:59698542
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-6230A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698542 | ||||||
| chr12:59698612
|
C | G | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-6160C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698612 | ||||||
| chr12:59698638
|
G | A | 3 | a0001c0001t0002g0152a0001c0001t0002g0157a0001c0001t0002g0198 | 3 | HG02148.hp2 HG04228.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-30-6134G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698638 | ||||||
| chr12:59698762
|
A | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-30-6010A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698762 | ||||||
| chr12:59698821
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5951G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698821 | ||||||
| chr12:59698893
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5879C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59698893 | ||||||
| chr12:59699002
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5770T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699002 | ||||||
| chr12:59699088
|
C | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30-5684C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699088 | ||||||
| chr12:59699159
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5613A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699159 | ||||||
| chr12:59699222
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5550T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699222 | ||||||
| chr12:59699327
|
A | G | 1 | a0002c0002t0003g0156 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-30-5445A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699327 | ||||||
| chr12:59699434
|
T | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-30-5338T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699434 | ||||||
| chr12:59699491
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5281T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699491 | ||||||
| chr12:59699655
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-5117T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699655 | ||||||
| chr12:59699755
|
T | G | 27 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30-5017T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59699755 | ||||||
| chr12:59700010
|
T | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-30-4762T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700010 | ||||||
| chr12:59700089
|
A | G | 1 | a0001c0003t0005g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-30-4683A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700089 | ||||||
| chr12:59700206
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-4566A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700206 | ||||||
| chr12:59700250
|
A | G | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-30-4522A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700250 | ||||||
| chr12:59700413
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-4359A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700413 | ||||||
| chr12:59700489
|
G | A | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-4283G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700489 | ||||||
| chr12:59700515
|
T | C | 3 | a0001c0001t0006g0253a0001c0001t0045g0013a0001c0001t0046g0002 | 3 | HG02559.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-30-4257T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700515 | ||||||
| chr12:59700641
|
T | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-4131T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700641 | ||||||
| chr12:59700647
|
C | T | 1 | a0001c0001t0018g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-30-4125C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700647 | ||||||
| chr12:59700820
|
T | C | 1 | a0002c0002t0004g0214 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-30-3952T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700820 | ||||||
| chr12:59700976
|
G | A | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30-3796G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59700976 | ||||||
| chr12:59701118
|
G | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-30-3654G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701118 | ||||||
| chr12:59701263
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-3509A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701263 | ||||||
| chr12:59701460
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-3312G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701460 | ||||||
| chr12:59701464
|
A | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(29): Show | 32 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-30-3308A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701464 | ||||||
| chr12:59701588
|
G | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0118 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-3184G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701588 | ||||||
| chr12:59701646
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-3126C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701646 | ||||||
| chr12:59701874
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-2898T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701874 | ||||||
| chr12:59701969
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-2803G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59701969 | ||||||
| chr12:59702062
|
C | G | 1 | a0002c0002t0003g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-30-2710C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702062 | ||||||
| chr12:59702149
|
A | C | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-2623A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702149 | ||||||
| chr12:59702282
|
A | G | 1 | a0001c0001t0032g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30-2490A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702282 | ||||||
| chr12:59702438
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-2334A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702438 | ||||||
| chr12:59702535
|
G | A | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30-2237G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702535 | ||||||
| chr12:59702668
|
G | A | 2 | a0001c0001t0010g0123a0001c0001t0048g0081 | 2 | HG00639.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-30-2104G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702668 | ||||||
| chr12:59702729
|
C | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30-2043C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702729 | ||||||
| chr12:59702755
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-30-2017T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702755 | ||||||
| chr12:59702835
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-1937C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702835 | ||||||
| chr12:59702962
|
A | C | 1 | a0001c0001t0032g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-30-1810A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702962 | ||||||
| chr12:59702976
|
C | T | 5 | a0001c0003t0005g0141a0001c0003t0005g0164a0001c0003t0005g0235others(2): Show | 5 | HG01261.hp2 HG02683.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-1796C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59702976 | ||||||
| chr12:59703336
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-1436G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703336 | ||||||
| chr12:59703343
|
A | G | 7 | a0002c0002t0003g0076a0002c0002t0008g0072a0002c0002t0008g0088others(4): Show | 7 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-1429A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703343 | ||||||
| chr12:59703880
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-892C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703880 | ||||||
| chr12:59703917
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-855G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703917 | ||||||
| chr12:59703929
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-843C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703929 | ||||||
| chr12:59703934
|
G | T | 1 | a0002c0002t0004g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-30-838G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703934 | ||||||
| chr12:59703957
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-815A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59703957 | ||||||
| chr12:59704045
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-727C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704045 | ||||||
| chr12:59704050
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-722A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704050 | ||||||
| chr12:59704098
|
T | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-674T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704098 | ||||||
| chr12:59704116
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0032a0002c0002t0004g0056others(1): Show | 4 | HG01928.hp2 HG02148.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-656C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704116 | ||||||
| chr12:59704199
|
C | CA | 17 | a0001c0001t0001g0163a0001c0001t0002g0055a0001c0001t0002g0058others(14): Show | 17 | HG00423.hp2 HG00673.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30-554dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59704199 | |||||
| chr12:59704199
|
CA | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(53): Show | 56 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.-30-554delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59704199 | |||||
| chr12:59704205
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-556_-30-537del others(20): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59704205 | |||||
| chr12:59704207
|
AAAAAAAA others(11): Show |
A | 6 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(3): Show | 6 | HG02257.hp1 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-554_-30-537del others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59704207 | |||||
| chr12:59704225
|
GA | G | 27 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-30-537delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 59704225 | |||||
| chr12:59704314
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-30-458A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704314 | ||||||
| chr12:59704445
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-327C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704445 | ||||||
| chr12:59704472
|
G | A | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-30-300G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704472 | ||||||
| chr12:59704474
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0012g0166a0001c0001t0012g0246others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-298A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704474 | ||||||
| chr12:59704640
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-132T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704640 | ||||||
| chr12:59704711
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-61G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704711 | ||||||
| chr12:59704760
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-12A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704760 | ||||||
| chr12:59704769
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.-30-3T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 2/5 | chr12 | 59704769 | ||||||
| chr12:59705209
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.217+191C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705209 | ||||||
| chr12:59705295
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+277G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705295 | ||||||
| chr12:59705627
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+609G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705627 | ||||||
| chr12:59705779
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0118 | 3 | HG01257.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.217+761C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705779 | ||||||
| chr12:59705853
|
T | C | 17 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.217+835T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705853 | ||||||
| chr12:59705918
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+900A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59705918 | ||||||
| chr12:59706018
|
C | T | 1 | a0002c0002t0003g0008 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.217+1000C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59706018 | ||||||
| chr12:59706055
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+1037A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59706055 | ||||||
| chr12:59706362
|
C | CTG | 127 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.217+1366_217+1367d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59706362 | |||||
| chr12:59706362
|
C | CTGTG | 39 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.217+1364_217+1367d others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59706362 | |||||
| chr12:59706362
|
C | CTGTGTG | 5 | a0001c0001t0006g0253a0001c0001t0041g0232a0001c0001t0045g0013others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+1362_217+1367d others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59706362 | |||||
| chr12:59706362
|
CTGTG | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0079a0001c0001t0001g0175 | 3 | NA18954.hp1 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.217+1364_217+1367d others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59706362 | |||||
| chr12:59706516
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.217+1498C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59706516 | ||||||
| chr12:59706644
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.217+1626A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59706644 | ||||||
| chr12:59706646
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.217+1628T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59706646 | ||||||
| chr12:59707046
|
A | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217+2028A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59707046 | ||||||
| chr12:59707283
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.217+2265G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59707283 | ||||||
| chr12:59707362
|
C | G | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.217+2344C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59707362 | ||||||
| chr12:59707766
|
G | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217+2748G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59707766 | ||||||
| chr12:59708230
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+3212C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59708230 | ||||||
| chr12:59708609
|
TTAGCCTA others(1550): Show |
T | 3 | a0001c0001t0006g0029a0001c0001t0006g0167a0001c0001t0006g0204 | 3 | HG01109.hp1 HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.217+3679_217+5235d others(2): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59708609 | |||||
| chr12:59708729
|
C | T | 1 | a0002c0002t0003g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.217+3711C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59708729 | ||||||
| chr12:59708973
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.217+3955C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59708973 | ||||||
| chr12:59709140
|
T | C | 164 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.217+4122T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709140 | ||||||
| chr12:59709216
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+4198A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709216 | ||||||
| chr12:59709314
|
G | A | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+4296G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709314 | ||||||
| chr12:59709409
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+4391G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709409 | ||||||
| chr12:59709451
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.217+4433G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709451 | ||||||
| chr12:59709542
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.217+4524G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709542 | ||||||
| chr12:59709666
|
G | C | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.217+4648G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709666 | ||||||
| chr12:59709668
|
A | T | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.217+4650A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709668 | ||||||
| chr12:59709680
|
C | A | 2 | a0001c0003t0005g0235a0001c0003t0005g0236 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.217+4662C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709680 | ||||||
| chr12:59709920
|
A | G | 1 | a0002c0002t0023g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.217+4902A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709920 | ||||||
| chr12:59709972
|
A | G | 3 | a0001c0001t0007g0097a0001c0001t0007g0158a0001c0001t0007g0168 | 3 | HG02451.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.217+4954A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59709972 | ||||||
| chr12:59710041
|
A | C | 11 | a0001c0001t0009g0243a0001c0001t0013g0069a0001c0001t0013g0073others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+5023A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710041 | ||||||
| chr12:59710098
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+5080T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710098 | ||||||
| chr12:59710134
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+5116T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710134 | ||||||
| chr12:59710259
|
C | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.217+5241C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710259 | ||||||
| chr12:59710605
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+5587T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710605 | ||||||
| chr12:59710636
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+5618C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710636 | ||||||
| chr12:59710683
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+5665C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710683 | ||||||
| chr12:59710726
|
A | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+5708A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710726 | ||||||
| chr12:59710738
|
A | G | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.217+5720A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710738 | ||||||
| chr12:59710753
|
T | C | 27 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(24): Show | 27 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.217+5735T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710753 | ||||||
| chr12:59710770
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+5752T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59710770 | ||||||
| chr12:59711126
|
G | T | 14 | a0001c0001t0006g0029a0001c0001t0006g0117a0001c0001t0006g0159others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.217+6108G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711126 | ||||||
| chr12:59711173
|
T | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(22): Show | 25 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.217+6155T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711173 | ||||||
| chr12:59711257
|
A | T | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+6239A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711257 | ||||||
| chr12:59711271
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+6253C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711271 | ||||||
| chr12:59711275
|
A | G | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+6257A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711275 | ||||||
| chr12:59711310
|
A | G | 28 | a0001c0001t0002g0011a0001c0001t0002g0051a0001c0001t0002g0193others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.217+6292A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711310 | ||||||
| chr12:59711438
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+6420A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711438 | ||||||
| chr12:59711458
|
AATGAAAT others(16): Show |
A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+6465_217+6487d others(25): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59711458 | |||||
| chr12:59711558
|
G | T | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.217+6540G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711558 | ||||||
| chr12:59711659
|
C | A | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+6641C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711659 | ||||||
| chr12:59711692
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.217+6674G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711692 | ||||||
| chr12:59711875
|
A | C | 1 | a0001c0001t0010g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.217+6857A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711875 | ||||||
| chr12:59711920
|
A | G | 5 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0002g0160others(2): Show | 5 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+6902A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59711920 | ||||||
| chr12:59712065
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7047A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712065 | ||||||
| chr12:59712174
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7156C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712174 | ||||||
| chr12:59712334
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02165.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.217+7316A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712334 | ||||||
| chr12:59712383
|
G | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.217+7365G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712383 | ||||||
| chr12:59712459
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7441G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712459 | ||||||
| chr12:59712570
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.217+7552G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712570 | ||||||
| chr12:59712628
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.217+7610A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712628 | ||||||
| chr12:59712732
|
C | T | 11 | a0001c0001t0009g0243a0001c0001t0013g0069a0001c0001t0013g0073others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+7714C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712732 | ||||||
| chr12:59712902
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7884A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712902 | ||||||
| chr12:59712954
|
G | A | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+7936G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712954 | ||||||
| chr12:59712954
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7936G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59712954 | ||||||
| chr12:59712991
|
GTTTTCTT others(3): Show |
G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+7988_217+7997d others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59712991 | |||||
| chr12:59713011
|
C | CT | 53 | a0001c0001t0001g0104a0001c0001t0001g0155a0001c0001t0001g0163others(50): Show | 53 | HG00741.hp1 HG01106.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.217+8002dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59713011 | |||||
| chr12:59713016
|
T | C | 1 | a0001c0001t0034g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.217+7998T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713016 | ||||||
| chr12:59713164
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+8146C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713164 | ||||||
| chr12:59713210
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.217+8192G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713210 | ||||||
| chr12:59713259
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+8241T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713259 | ||||||
| chr12:59713310
|
G | A | 2 | a0001c0003t0005g0235a0001c0003t0005g0236 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.217+8292G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713310 | ||||||
| chr12:59713315
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+8297C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713315 | ||||||
| chr12:59713453
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+8435T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713453 | ||||||
| chr12:59713533
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+8515T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713533 | ||||||
| chr12:59713886
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+8868G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59713886 | ||||||
| chr12:59714036
|
C | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(54): Show | 57 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.217+9018C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714036 | ||||||
| chr12:59714066
|
G | A | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.217+9048G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714066 | ||||||
| chr12:59714095
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+9077G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714095 | ||||||
| chr12:59714179
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.217+9161C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714179 | ||||||
| chr12:59714237
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+9219A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714237 | ||||||
| chr12:59714283
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+9265T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714283 | ||||||
| chr12:59714389
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.217+9371A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714389 | ||||||
| chr12:59714394
|
T | C | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+9376T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714394 | ||||||
| chr12:59714525
|
C | A | 1 | a0002c0002t0004g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.217+9507C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714525 | ||||||
| chr12:59714526
|
A | G | 1 | a0002c0002t0003g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.217+9508A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714526 | ||||||
| chr12:59714549
|
T | TTCTC | 24 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(21): Show | 24 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.217+9545_217+9548d others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59714549 | |||||
| chr12:59714698
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.217+9680A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714698 | ||||||
| chr12:59714761
|
C | T | 3 | a0001c0001t0006g0253a0001c0001t0045g0013a0001c0001t0046g0002 | 3 | HG02559.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.217+9743C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714761 | ||||||
| chr12:59714762
|
G | A | 11 | a0001c0001t0009g0243a0001c0001t0013g0069a0001c0001t0013g0073others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.217+9744G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714762 | ||||||
| chr12:59714766
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+9748C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714766 | ||||||
| chr12:59714800
|
G | A | 1 | a0002c0002t0004g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.217+9782G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714800 | ||||||
| chr12:59714812
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.217+9794G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714812 | ||||||
| chr12:59714823
|
C | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0118 | 3 | HG01257.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.217+9805C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714823 | ||||||
| chr12:59714860
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217+9842C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59714860 | ||||||
| chr12:59715094
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+10076A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715094 | ||||||
| chr12:59715096
|
T | C | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.217+10078T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715096 | ||||||
| chr12:59715175
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+10157C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715175 | ||||||
| chr12:59715329
|
G | A | 26 | a0001c0001t0002g0011a0001c0001t0002g0051a0001c0001t0002g0193others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.217+10311G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715329 | ||||||
| chr12:59715456
|
G | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217+10438G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715456 | ||||||
| chr12:59715465
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+10447T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715465 | ||||||
| chr12:59715468
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+10450G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715468 | ||||||
| chr12:59715590
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0012g0166a0001c0001t0012g0246others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+10572A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715590 | ||||||
| chr12:59715624
|
G | T | 11 | a0001c0001t0009g0243a0001c0001t0013g0069a0001c0001t0013g0073others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+10606G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715624 | ||||||
| chr12:59715699
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+10681G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59715699 | ||||||
| chr12:59715866
|
AGTTT | A | 5 | a0001c0001t0006g0117a0001c0001t0006g0159a0001c0001t0006g0172others(2): Show | 5 | HG02630.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+10853_217+1085 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59715866 | |||||
| chr12:59716097
|
T | C | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+11079T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716097 | ||||||
| chr12:59716119
|
A | G | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+11101A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716119 | ||||||
| chr12:59716226
|
T | G | 3 | a0001c0001t0006g0253a0001c0001t0045g0013a0001c0001t0046g0002 | 3 | HG02559.hp1 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.217+11208T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716226 | ||||||
| chr12:59716238
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+11220T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716238 | ||||||
| chr12:59716247
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.217+11229C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716247 | ||||||
| chr12:59716324
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+11306G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716324 | ||||||
| chr12:59716334
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+11316G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716334 | ||||||
| chr12:59716367
|
CTCT | C | 4 | a0001c0001t0002g0055a0001c0001t0002g0061a0001c0001t0002g0132others(1): Show | 4 | HG00741.hp2 HG01496.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+11357_217+1135 others(7): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59716367 | |||||
| chr12:59716439
|
G | A | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.217+11421G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716439 | ||||||
| chr12:59716458
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+11440A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716458 | ||||||
| chr12:59716544
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+11526C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716544 | ||||||
| chr12:59716558
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+11540C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716558 | ||||||
| chr12:59716624
|
G | T | 1 | a0002c0002t0003g0111 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.217+11606G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716624 | ||||||
| chr12:59716681
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+11663C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716681 | ||||||
| chr12:59716899
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.217+11881A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59716899 | ||||||
| chr12:59717232
|
A | G | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+12214A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717232 | ||||||
| chr12:59717278
|
T | A | 3 | a0002c0002t0008g0206a0002c0002t0008g0227a0002c0002t0008g0251 | 3 | HG02976.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.217+12260T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717278 | ||||||
| chr12:59717344
|
G | A | 1 | a0001c0001t0007g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.217+12326G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717344 | ||||||
| chr12:59717365
|
G | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+12347G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717365 | ||||||
| chr12:59717374
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+12356G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717374 | ||||||
| chr12:59717411
|
G | A | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.217+12393G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717411 | ||||||
| chr12:59717490
|
C | T | 1 | a0001c0003t0005g0087 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.217+12472C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717490 | ||||||
| chr12:59717545
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.217+12527A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717545 | ||||||
| chr12:59717608
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+12590C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717608 | ||||||
| chr12:59717872
|
A | G | 36 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 36 | HG00099.hp2 HG00673.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.217+12854A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59717872 | ||||||
| chr12:59718359
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+13341T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718359 | ||||||
| chr12:59718387
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+13369C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718387 | ||||||
| chr12:59718389
|
A | G | 2 | a0001c0001t0018g0005a0001c0001t0018g0096 | 2 | NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.217+13371A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718389 | ||||||
| chr12:59718392
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+13374A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718392 | ||||||
| chr12:59718438
|
G | A | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.217+13420G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718438 | ||||||
| chr12:59718779
|
T | C | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.217+13761T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718779 | ||||||
| chr12:59718788
|
A | G | 26 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+13770A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718788 | ||||||
| chr12:59718818
|
A | T | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.217+13800A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718818 | ||||||
| chr12:59718826
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+13808G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59718826 | ||||||
| chr12:59719120
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00639.hp1 HG00738.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.217+14102T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719120 | ||||||
| chr12:59719193
|
A | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+14175A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719193 | ||||||
| chr12:59719204
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+14186A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719204 | ||||||
| chr12:59719423
|
C | T | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217+14405C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719423 | ||||||
| chr12:59719446
|
A | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+14428A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719446 | ||||||
| chr12:59719529
|
A | C | 2 | a0001c0001t0007g0103a0001c0001t0007g0128 | 2 | HG00735.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.217+14511A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719529 | ||||||
| chr12:59719663
|
ATCT | A | 38 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(35): Show | 38 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.217+14650_217+1465 others(7): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59719663 | |||||
| chr12:59719893
|
G | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.217+14875G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719893 | ||||||
| chr12:59719903
|
A | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+14885A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719903 | ||||||
| chr12:59719946
|
A | G | 21 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.217+14928A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719946 | ||||||
| chr12:59719948
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+14930G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59719948 | ||||||
| chr12:59720077
|
A | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+15059A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720077 | ||||||
| chr12:59720129
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15111A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720129 | ||||||
| chr12:59720155
|
C | CAG | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15138_217+1513 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59720155 | |||||
| chr12:59720320
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15302G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720320 | ||||||
| chr12:59720336
|
T | C | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+15318T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720336 | ||||||
| chr12:59720337
|
A | T | 1 | a0002c0002t0003g0156 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.217+15319A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720337 | ||||||
| chr12:59720357
|
A | G | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.217+15339A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720357 | ||||||
| chr12:59720369
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15351C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720369 | ||||||
| chr12:59720414
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15396A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720414 | ||||||
| chr12:59720437
|
A | G | 1 | a0002c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.217+15419A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720437 | ||||||
| chr12:59720544
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.217+15526A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720544 | ||||||
| chr12:59720595
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+15577G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720595 | ||||||
| chr12:59720790
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.217+15772A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720790 | ||||||
| chr12:59720919
|
A | G | 1 | a0001c0003t0005g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.217+15901A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59720919 | ||||||
| chr12:59721040
|
C | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+16022C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721040 | ||||||
| chr12:59721072
|
G | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+16054G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721072 | ||||||
| chr12:59721250
|
T | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+16232T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721250 | ||||||
| chr12:59721437
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.217+16419G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721437 | ||||||
| chr12:59721437
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+16419G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721437 | ||||||
| chr12:59721588
|
G | C | 121 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.217+16570G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721588 | ||||||
| chr12:59721690
|
C | T | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.217+16672C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721690 | ||||||
| chr12:59721730
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0028 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.217+16712A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721730 | ||||||
| chr12:59721812
|
C | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+16794C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59721812 | ||||||
| chr12:59722085
|
A | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0111 | 2 | HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.217+17067A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722085 | ||||||
| chr12:59722088
|
T | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.217+17070T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722088 | ||||||
| chr12:59722193
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+17175A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722193 | ||||||
| chr12:59722268
|
A | G | 1 | a0001c0001t0007g0139 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.217+17250A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722268 | ||||||
| chr12:59722324
|
C | G | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+17306C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722324 | ||||||
| chr12:59722543
|
C | G | 16 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(13): Show | 16 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.217+17525C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722543 | ||||||
| chr12:59722668
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.217+17650C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722668 | ||||||
| chr12:59722752
|
G | A | 2 | a0002c0002t0003g0184a0005c0009t0003g0187 | 2 | NA18954.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.217+17734G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722752 | ||||||
| chr12:59722862
|
A | G | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.217+17844A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59722862 | ||||||
| chr12:59723120
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18102G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723120 | ||||||
| chr12:59723199
|
T | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+18181T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723199 | ||||||
| chr12:59723238
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18220T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723238 | ||||||
| chr12:59723405
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18387G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723405 | ||||||
| chr12:59723470
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18452T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723470 | ||||||
| chr12:59723550
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+18532T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723550 | ||||||
| chr12:59723590
|
T | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+18572T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723590 | ||||||
| chr12:59723668
|
C | T | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217+18650C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723668 | ||||||
| chr12:59723728
|
T | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+18710T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723728 | ||||||
| chr12:59723765
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18747T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723765 | ||||||
| chr12:59723821
|
G | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217+18803G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723821 | ||||||
| chr12:59723846
|
G | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+18828G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723846 | ||||||
| chr12:59723858
|
T | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+18840T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723858 | ||||||
| chr12:59723931
|
C | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+18913C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723931 | ||||||
| chr12:59723994
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+18976A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59723994 | ||||||
| chr12:59724037
|
T | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+19019T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724037 | ||||||
| chr12:59724134
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.217+19116C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724134 | ||||||
| chr12:59724141
|
G | T | 1 | a0001c0003t0005g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.217+19123G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724141 | ||||||
| chr12:59724189
|
G | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+19171G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724189 | ||||||
| chr12:59724467
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+19449A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724467 | ||||||
| chr12:59724630
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+19612G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724630 | ||||||
| chr12:59724651
|
G | T | 1 | a0001c0001t0002g0127 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.217+19633G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724651 | ||||||
| chr12:59724741
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+19723G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724741 | ||||||
| chr12:59724860
|
G | A | 1 | a0001c0001t0032g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.217+19842G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724860 | ||||||
| chr12:59724978
|
A | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+19960A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59724978 | ||||||
| chr12:59724998
|
A | ACCTATTG others(320): Show |
1 | a0001c0001t0006g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.217+19996_217+1999 others(331): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59724998
|
A | ACCTATTG others(321): Show |
6 | a0001c0001t0006g0001a0001c0001t0006g0117a0001c0001t0006g0172others(3): Show | 6 | HG01891.hp1 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+19996_217+1999 others(332): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59724998
|
A | ACCTATTG others(322): Show |
3 | a0001c0001t0006g0029a0001c0001t0006g0167a0001c0001t0015g0004 | 3 | HG01109.hp1 HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.217+19996_217+1999 others(333): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59724998
|
A | ACCTATTG others(323): Show |
4 | a0001c0001t0006g0171a0001c0001t0006g0222a0001c0001t0006g0253others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+19996_217+1999 others(334): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59724998
|
A | ACCTATTG others(324): Show |
3 | a0001c0001t0006g0221a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | HG02109.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.217+19996_217+1999 others(335): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59724998
|
A | ACCTATTG others(325): Show |
1 | a0001c0001t0006g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.217+19996_217+1999 others(336): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59724998 | |||||
| chr12:59725042
|
A | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+20024A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725042 | ||||||
| chr12:59725149
|
T | G | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+20131T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725149 | ||||||
| chr12:59725158
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+20140G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725158 | ||||||
| chr12:59725409
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+20391C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725409 | ||||||
| chr12:59725630
|
T | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217+20612T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725630 | ||||||
| chr12:59725697
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.217+20679C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725697 | ||||||
| chr12:59725712
|
G | A | 133 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.217+20694G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725712 | ||||||
| chr12:59725733
|
G | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+20715G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725733 | ||||||
| chr12:59725797
|
G | A | 39 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.217+20779G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725797 | ||||||
| chr12:59725797
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+20779G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725797 | ||||||
| chr12:59725869
|
T | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+20851T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725869 | ||||||
| chr12:59725962
|
G | T | 26 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+20944G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59725962 | ||||||
| chr12:59726147
|
G | A | 72 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.217+21129G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726147 | ||||||
| chr12:59726148
|
A | G | 72 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.217+21130A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726148 | ||||||
| chr12:59726351
|
T | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+21333T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726351 | ||||||
| chr12:59726375
|
G | A | 1 | a0002c0002t0003g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.217+21357G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726375 | ||||||
| chr12:59726569
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+21551T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726569 | ||||||
| chr12:59726671
|
G | T | 1 | a0001c0001t0007g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.217+21653G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726671 | ||||||
| chr12:59726740
|
C | G | 1 | a0001c0001t0038g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.217+21722C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726740 | ||||||
| chr12:59726862
|
T | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+21844T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726862 | ||||||
| chr12:59726888
|
T | C | 11 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+21870T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726888 | ||||||
| chr12:59726946
|
G | GA | 10 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.217+21932dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59726946 | |||||
| chr12:59726981
|
T | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+21963T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59726981 | ||||||
| chr12:59727030
|
T | C | 15 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(12): Show | 15 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.217+22012T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727030 | ||||||
| chr12:59727073
|
T | C | 121 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.217+22055T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727073 | ||||||
| chr12:59727074
|
G | A | 7 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(4): Show | 7 | HG01175.hp1 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.217+22056G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727074 | ||||||
| chr12:59727133
|
T | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0126others(2): Show | 5 | HG00408.hp2 NA18947.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+22115T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727133 | ||||||
| chr12:59727151
|
C | CAT | 16 | a0001c0001t0007g0031a0001c0001t0007g0070a0001c0001t0013g0069others(13): Show | 16 | HG01978.hp1 HG02257.hp1 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.217+22151_217+2215 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727151 | |||||
| chr12:59727151
|
C | CATAT | 16 | a0001c0001t0002g0057a0001c0001t0002g0131a0001c0001t0002g0179others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.217+22149_217+2215 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727151 | |||||
| chr12:59727151
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+22133C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727151 | ||||||
| chr12:59727151
|
CAT | C | 30 | a0001c0001t0001g0125a0002c0002t0003g0094a0002c0002t0003g0100others(27): Show | 30 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.217+22151_217+2215 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727151 | |||||
| chr12:59727154
|
A | ATATATAT others(4): Show |
17 | a0001c0003t0005g0009a0001c0003t0005g0012a0001c0003t0005g0074others(14): Show | 17 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.217+22137_217+2214 others(15): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727154 | |||||
| chr12:59727154
|
A | ATATATAT others(6): Show |
1 | a0001c0003t0005g0007 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.217+22147_217+2214 others(17): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727154 | |||||
| chr12:59727170
|
A | AAT | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+22161_217+2216 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727170 | |||||
| chr12:59727170
|
A | ATATATAA others(20): Show |
1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+22152_217+2215 others(31): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727170
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0006g0001a0001c0001t0006g0253 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.217+22152_217+2215 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727170
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0006g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.217+22152_217+2215 others(20): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727170
|
A | ATATATAT others(11): Show |
6 | a0001c0001t0006g0029a0001c0001t0006g0159a0001c0001t0006g0171others(3): Show | 6 | HG02572.hp1 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+22152_217+2215 others(22): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727170
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0006g0225a0001c0001t0006g0226a0001c0001t0015g0004others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+22152_217+2215 others(24): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727170
|
A | ATATATAT others(15): Show |
4 | a0001c0001t0006g0167a0001c0001t0006g0221a0001c0001t0006g0222others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+22152_217+2215 others(26): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727170 | ||||||
| chr12:59727348
|
G | A | 1 | a0001c0001t0044g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.217+22330G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727348 | ||||||
| chr12:59727486
|
G | A | 1 | a0001c0001t0010g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.217+22468G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727486 | ||||||
| chr12:59727539
|
A | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+22521A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727539 | ||||||
| chr12:59727669
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+22651C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727669 | ||||||
| chr12:59727682
|
G | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+22664G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727682 | ||||||
| chr12:59727783
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.217+22765G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727783 | ||||||
| chr12:59727805
|
TG | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+22794delG | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59727805 | |||||
| chr12:59727823
|
A | G | 15 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(12): Show | 15 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.217+22805A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727823 | ||||||
| chr12:59727865
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+22847A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59727865 | ||||||
| chr12:59728048
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+23030T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728048 | ||||||
| chr12:59728055
|
T | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+23037T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728055 | ||||||
| chr12:59728115
|
G | A | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+23097G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728115 | ||||||
| chr12:59728580
|
C | G | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.217+23562C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728580 | ||||||
| chr12:59728612
|
C | G | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+23594C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728612 | ||||||
| chr12:59728710
|
A | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+23692A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728710 | ||||||
| chr12:59728726
|
T | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+23708T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728726 | ||||||
| chr12:59728807
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.217+23789C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728807 | ||||||
| chr12:59728964
|
G | A | 1 | a0001c0001t0030g0018 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.217+23946G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59728964 | ||||||
| chr12:59729196
|
C | T | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.217+24178C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729196 | ||||||
| chr12:59729205
|
G | A | 4 | a0002c0002t0008g0206a0002c0002t0008g0227a0002c0002t0008g0251others(1): Show | 4 | HG02976.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+24187G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729205 | ||||||
| chr12:59729361
|
T | G | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+24343T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729361 | ||||||
| chr12:59729408
|
C | T | 1 | a0001c0001t0006g0167 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.217+24390C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729408 | ||||||
| chr12:59729470
|
T | A | 1 | a0004c0005t0009g0089 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.217+24452T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729470 | ||||||
| chr12:59729475
|
A | T | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.217+24457A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729475 | ||||||
| chr12:59729544
|
T | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+24526T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729544 | ||||||
| chr12:59729790
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+24772C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729790 | ||||||
| chr12:59729849
|
A | C | 1 | a0002c0002t0003g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.217+24831A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729849 | ||||||
| chr12:59729884
|
T | G | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217+24866T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59729884 | ||||||
| chr12:59730212
|
GA | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 41 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.217+25206delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59730212 | |||||
| chr12:59730212
|
GAA | G | 119 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.217+25205_217+2520 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59730212 | |||||
| chr12:59730245
|
G | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217+25227G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730245 | ||||||
| chr12:59730308
|
A | G | 72 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.217+25290A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730308 | ||||||
| chr12:59730347
|
TAA | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.217+25343_217+2534 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59730347 | |||||
| chr12:59730376
|
T | A | 1 | a0001c0003t0005g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.217+25358T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730376 | ||||||
| chr12:59730525
|
AAAT | A | 8 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0025g0248others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+25525_217+2552 others(7): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59730525 | |||||
| chr12:59730541
|
A | C | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.217+25523A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730541 | ||||||
| chr12:59730547
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+25529G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730547 | ||||||
| chr12:59730719
|
G | A | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.217+25701G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730719 | ||||||
| chr12:59730782
|
A | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217+25764A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59730782 | ||||||
| chr12:59731002
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+25984T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731002 | ||||||
| chr12:59731093
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+26075T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731093 | ||||||
| chr12:59731156
|
A | G | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+26138A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731156 | ||||||
| chr12:59731161
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+26143C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731161 | ||||||
| chr12:59731172
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.217+26154T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731172 | ||||||
| chr12:59731652
|
G | A | 1 | a0002c0002t0004g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.217+26634G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731652 | ||||||
| chr12:59731721
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+26703C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731721 | ||||||
| chr12:59731925
|
T | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+26907T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59731925 | ||||||
| chr12:59732064
|
T | TTA | 17 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(14): Show | 17 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.217+27056_217+2705 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59732064 | |||||
| chr12:59732151
|
C | T | 1 | a0001c0001t0007g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.217+27133C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732151 | ||||||
| chr12:59732222
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+27204G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732222 | ||||||
| chr12:59732302
|
C | A | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.217+27284C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732302 | ||||||
| chr12:59732324
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.217+27306G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732324 | ||||||
| chr12:59732357
|
T | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+27339T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732357 | ||||||
| chr12:59732689
|
A | G | 1 | a0001c0001t0006g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+27671A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732689 | ||||||
| chr12:59732792
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+27774G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732792 | ||||||
| chr12:59732817
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+27799C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59732817 | ||||||
| chr12:59733067
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+28049T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733067 | ||||||
| chr12:59733145
|
A | G | 111 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.217+28127A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733145 | ||||||
| chr12:59733147
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.217+28129C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733147 | ||||||
| chr12:59733170
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28152G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733170 | ||||||
| chr12:59733249
|
C | T | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217+28231C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733249 | ||||||
| chr12:59733277
|
A | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+28259A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733277 | ||||||
| chr12:59733309
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+28291G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733309 | ||||||
| chr12:59733364
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28346G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733364 | ||||||
| chr12:59733380
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+28362G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733380 | ||||||
| chr12:59733386
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28368C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733386 | ||||||
| chr12:59733392
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28374G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733392 | ||||||
| chr12:59733450
|
A | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28432A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733450 | ||||||
| chr12:59733479
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+28461G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733479 | ||||||
| chr12:59733543
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+28525A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733543 | ||||||
| chr12:59733571
|
G | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+28553G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733571 | ||||||
| chr12:59733599
|
G | C | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+28581G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733599 | ||||||
| chr12:59733775
|
C | T | 4 | a0001c0001t0009g0243a0002c0002t0004g0214a0002c0002t0004g0217others(1): Show | 4 | HG01358.hp1 HG03139.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+28757C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733775 | ||||||
| chr12:59733809
|
A | T | 120 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.217+28791A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733809 | ||||||
| chr12:59733831
|
G | A | 120 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.217+28813G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733831 | ||||||
| chr12:59733945
|
G | A | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.217+28927G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733945 | ||||||
| chr12:59733999
|
G | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+28981G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59733999 | ||||||
| chr12:59734248
|
C | G | 1 | a0001c0001t0033g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.217+29230C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734248 | ||||||
| chr12:59734536
|
A | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+29518A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734536 | ||||||
| chr12:59734574
|
A | G | 111 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.217+29556A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734574 | ||||||
| chr12:59734672
|
C | G | 72 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.217+29654C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734672 | ||||||
| chr12:59734755
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+29737T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734755 | ||||||
| chr12:59734868
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.217+29850A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734868 | ||||||
| chr12:59734871
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+29853C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59734871 | ||||||
| chr12:59735191
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+30173G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735191 | ||||||
| chr12:59735194
|
G | T | 2 | a0001c0003t0005g0116a0001c0003t0005g0203 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.217+30176G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735194 | ||||||
| chr12:59735315
|
C | A | 132 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(129): Show | 132 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.217+30297C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735315 | ||||||
| chr12:59735361
|
G | A | 2 | a0001c0003t0005g0087a0001c0003t0005g0091 | 2 | NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.217+30343G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735361 | ||||||
| chr12:59735420
|
G | A | 9 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0073others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+30402G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735420 | ||||||
| chr12:59735467
|
C | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217+30449C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735467 | ||||||
| chr12:59735624
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+30606G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735624 | ||||||
| chr12:59735712
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+30694T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735712 | ||||||
| chr12:59735859
|
T | C | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.217+30841T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735859 | ||||||
| chr12:59735992
|
A | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+30974A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59735992 | ||||||
| chr12:59736075
|
T | A | 10 | a0001c0001t0002g0057a0001c0001t0002g0065a0001c0001t0002g0086others(7): Show | 10 | HG00609.hp2 HG02155.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.217+31057T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736075 | ||||||
| chr12:59736080
|
G | A | 1 | a0001c0001t0010g0237 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.217+31062G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736080 | ||||||
| chr12:59736115
|
A | T | 111 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.217+31097A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736115 | ||||||
| chr12:59736137
|
G | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+31119G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736137 | ||||||
| chr12:59736263
|
G | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+31245G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736263 | ||||||
| chr12:59736271
|
G | A | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+31253G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736271 | ||||||
| chr12:59736365
|
A | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+31347A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736365 | ||||||
| chr12:59736401
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.217+31383T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736401 | ||||||
| chr12:59736407
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+31389G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736407 | ||||||
| chr12:59736507
|
G | A | 2 | a0002c0002t0004g0077a0002c0002t0004g0095 | 2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.217+31489G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736507 | ||||||
| chr12:59736535
|
G | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02165.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.217+31517G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736535 | ||||||
| chr12:59736570
|
G | C | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+31552G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736570 | ||||||
| chr12:59736642
|
T | C | 63 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.217+31624T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736642 | ||||||
| chr12:59736737
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.217+31719A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736737 | ||||||
| chr12:59736779
|
G | A | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.217+31761G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736779 | ||||||
| chr12:59736822
|
C | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+31804C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736822 | ||||||
| chr12:59736843
|
C | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.217+31825C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736843 | ||||||
| chr12:59736886
|
T | A | 2 | a0001c0003t0005g0116a0001c0003t0005g0203 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.217+31868T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59736886 | ||||||
| chr12:59737295
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+32277T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737295 | ||||||
| chr12:59737438
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.217+32420G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737438 | ||||||
| chr12:59737627
|
T | C | 2 | a0001c0001t0006g0172a0001c0001t0006g0207 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.217+32609T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737627 | ||||||
| chr12:59737666
|
G | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0193a0001c0001t0002g0213 | 3 | HG00408.hp1 HG00423.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.217+32648G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737666 | ||||||
| chr12:59737734
|
C | A | 1 | a0001c0001t0007g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.217+32716C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737734 | ||||||
| chr12:59737805
|
T | C | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.217+32787T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737805 | ||||||
| chr12:59737817
|
C | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.217+32799C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59737817 | ||||||
| chr12:59738005
|
T | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217+32987T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738005 | ||||||
| chr12:59738093
|
T | C | 1 | a0001c0003t0005g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.217+33075T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738093 | ||||||
| chr12:59738344
|
A | G | 1 | a0002c0002t0004g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.218-32875A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738344 | ||||||
| chr12:59738429
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.218-32790A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738429 | ||||||
| chr12:59738505
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-32714C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738505 | ||||||
| chr12:59738658
|
T | G | 1 | a0002c0002t0003g0111 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.218-32561T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738658 | ||||||
| chr12:59738706
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-32513C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738706 | ||||||
| chr12:59738723
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.218-32496A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738723 | ||||||
| chr12:59738759
|
T | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-32460T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738759 | ||||||
| chr12:59738832
|
T | TC | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-32387_218-3238 others(5): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738832 | ||||||
| chr12:59738833
|
T | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-32386T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738833 | ||||||
| chr12:59738845
|
G | C | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-32374G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738845 | ||||||
| chr12:59738996
|
G | C | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-32223G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59738996 | ||||||
| chr12:59739017
|
TTCATTTA | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-32200_218-3219 others(11): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59739017 | |||||
| chr12:59739019
|
CATTT | C | 74 | a0001c0001t0002g0224a0001c0001t0006g0171a0001c0001t0006g0226others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.218-32175_218-3217 others(8): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59739019 | |||||
| chr12:59739019
|
CATTTATT others(1): Show |
C | 16 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-32179_218-3217 others(12): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59739019 | |||||
| chr12:59739027
|
T | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-32192T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739027 | ||||||
| chr12:59739136
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-32083A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739136 | ||||||
| chr12:59739193
|
C | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0215 | 3 | HG00140.hp2 HG00438.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.218-32026C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739193 | ||||||
| chr12:59739248
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31971A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739248 | ||||||
| chr12:59739290
|
G | A | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-31929G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739290 | ||||||
| chr12:59739456
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31763C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739456 | ||||||
| chr12:59739492
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31727C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739492 | ||||||
| chr12:59739493
|
G | C | 2 | a0002c0002t0004g0056a0002c0002t0004g0098 | 2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.218-31726G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739493 | ||||||
| chr12:59739506
|
G | A | 1 | a0001c0001t0010g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218-31713G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739506 | ||||||
| chr12:59739519
|
T | C | 1 | a0001c0001t0002g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.218-31700T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739519 | ||||||
| chr12:59739540
|
G | A | 9 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-31679G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739540 | ||||||
| chr12:59739565
|
G | C | 14 | a0001c0001t0006g0029a0001c0001t0006g0117a0001c0001t0006g0159others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.218-31654G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739565 | ||||||
| chr12:59739755
|
A | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-31464A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739755 | ||||||
| chr12:59739770
|
A | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31449A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739770 | ||||||
| chr12:59739793
|
A | C | 4 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-31426A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739793 | ||||||
| chr12:59739812
|
T | A | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.218-31407T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59739812 | ||||||
| chr12:59740019
|
C | G | 1 | a0001c0003t0005g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.218-31200C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740019 | ||||||
| chr12:59740027
|
G | C | 1 | a0001c0003t0005g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.218-31192G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740027 | ||||||
| chr12:59740064
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31155C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740064 | ||||||
| chr12:59740076
|
T | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-31143T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740076 | ||||||
| chr12:59740078
|
G | C | 1 | a0001c0001t0002g0146 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.218-31141G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740078 | ||||||
| chr12:59740162
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-31057C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740162 | ||||||
| chr12:59740185
|
G | A | 1 | a0002c0002t0004g0099 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218-31034G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740185 | ||||||
| chr12:59740225
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-30994G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740225 | ||||||
| chr12:59740257
|
A | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-30962A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740257 | ||||||
| chr12:59740305
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-30914C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740305 | ||||||
| chr12:59740363
|
G | A | 2 | a0002c0002t0003g0008a0002c0002t0003g0228 | 2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.218-30856G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740363 | ||||||
| chr12:59740461
|
T | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218-30758T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740461 | ||||||
| chr12:59740513
|
C | A | 1 | a0001c0001t0002g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-30706C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740513 | ||||||
| chr12:59740692
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0028g0133 | 2 | NA18969.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.218-30527T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740692 | ||||||
| chr12:59740740
|
G | A | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-30479G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740740 | ||||||
| chr12:59740786
|
T | A | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.218-30433T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740786 | ||||||
| chr12:59740794
|
C | T | 132 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(129): Show | 132 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.218-30425C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740794 | ||||||
| chr12:59740842
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-30377T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740842 | ||||||
| chr12:59740882
|
T | G | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-30337T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59740882 | ||||||
| chr12:59741075
|
T | G | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218-30144T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741075 | ||||||
| chr12:59741099
|
T | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-30120T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741099 | ||||||
| chr12:59741179
|
G | A | 38 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(35): Show | 38 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.218-30040G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741179 | ||||||
| chr12:59741182
|
G | T | 2 | a0001c0001t0006g0167a0001c0001t0018g0096 | 2 | HG01109.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.218-30037G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741182 | ||||||
| chr12:59741238
|
G | C | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-29981G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741238 | ||||||
| chr12:59741431
|
T | C | 72 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-29788T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741431 | ||||||
| chr12:59741447
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-29772G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741447 | ||||||
| chr12:59741517
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-29702G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741517 | ||||||
| chr12:59741519
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-29700C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741519 | ||||||
| chr12:59741621
|
G | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.218-29598G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741621 | ||||||
| chr12:59741723
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-29496G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741723 | ||||||
| chr12:59741792
|
C | T | 11 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-29427C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741792 | ||||||
| chr12:59741889
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.218-29330T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59741889 | ||||||
| chr12:59742017
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.218-29202T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742017 | ||||||
| chr12:59742242
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.218-28977C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742242 | ||||||
| chr12:59742509
|
G | T | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218-28710G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742509 | ||||||
| chr12:59742527
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-28692G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742527 | ||||||
| chr12:59742529
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-28690G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742529 | ||||||
| chr12:59742603
|
T | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-28616T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742603 | ||||||
| chr12:59742715
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-28504T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742715 | ||||||
| chr12:59742724
|
C | A | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.218-28495C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59742724 | ||||||
| chr12:59743248
|
A | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-27971A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743248 | ||||||
| chr12:59743276
|
G | A | 1 | a0001c0001t0036g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.218-27943G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743276 | ||||||
| chr12:59743313
|
C | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-27906C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743313 | ||||||
| chr12:59743631
|
G | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0143a0001c0001t0001g0150 | 3 | NA18947.hp2 NA18978.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.218-27588G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743631 | ||||||
| chr12:59743760
|
A | C | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.218-27459A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743760 | ||||||
| chr12:59743864
|
C | T | 71 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.218-27355C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59743864 | ||||||
| chr12:59744018
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-27201G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744018 | ||||||
| chr12:59744072
|
T | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218-27147T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744072 | ||||||
| chr12:59744134
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-27085C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744134 | ||||||
| chr12:59744143
|
T | C | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-27076T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744143 | ||||||
| chr12:59744161
|
C | G | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218-27058C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744161 | ||||||
| chr12:59744249
|
C | T | 1 | a0001c0001t0031g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.218-26970C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744249 | ||||||
| chr12:59744268
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-26951A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744268 | ||||||
| chr12:59744292
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-26927G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744292 | ||||||
| chr12:59744330
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-26889T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744330 | ||||||
| chr12:59744341
|
C | T | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218-26878C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744341 | ||||||
| chr12:59744397
|
A | T | 1 | a0001c0001t0032g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.218-26822A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744397 | ||||||
| chr12:59744453
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.218-26766C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744453 | ||||||
| chr12:59744516
|
C | T | 63 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.218-26703C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744516 | ||||||
| chr12:59744747
|
G | A | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218-26472G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744747 | ||||||
| chr12:59744856
|
T | G | 1 | a0001c0001t0018g0005 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218-26363T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59744856 | ||||||
| chr12:59745130
|
G | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-26089G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745130 | ||||||
| chr12:59745159
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-26060G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745159 | ||||||
| chr12:59745165
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.218-26054G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745165 | ||||||
| chr12:59745282
|
A | T | 1 | a0001c0001t0002g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.218-25937A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745282 | ||||||
| chr12:59745357
|
G | T | 1 | a0002c0002t0003g0107 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.218-25862G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745357 | ||||||
| chr12:59745398
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-25821C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745398 | ||||||
| chr12:59745473
|
AAGATTTA others(7): Show |
A | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-25744_218-2573 others(18): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59745473 | |||||
| chr12:59745547
|
C | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-25672C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745547 | ||||||
| chr12:59745577
|
C | A | 1 | a0001c0001t0038g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.218-25642C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745577 | ||||||
| chr12:59745655
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218-25564C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745655 | ||||||
| chr12:59745671
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-25548C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745671 | ||||||
| chr12:59745777
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-25442G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745777 | ||||||
| chr12:59745800
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-25419G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59745800 | ||||||
| chr12:59746041
|
G | A | 65 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.218-25178G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746041 | ||||||
| chr12:59746074
|
T | C | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-25145T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746074 | ||||||
| chr12:59746187
|
T | C | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.218-25032T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746187 | ||||||
| chr12:59746201
|
T | C | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218-25018T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746201 | ||||||
| chr12:59746304
|
C | T | 26 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-24915C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746304 | ||||||
| chr12:59746336
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-24883G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746336 | ||||||
| chr12:59746534
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218-24685A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746534 | ||||||
| chr12:59746562
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218-24657G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746562 | ||||||
| chr12:59746750
|
T | A | 1 | a0001c0003t0010g0019 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.218-24469T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746750 | ||||||
| chr12:59746814
|
T | G | 7 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-24405T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746814 | ||||||
| chr12:59746957
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-24262C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59746957 | ||||||
| chr12:59747032
|
G | A | 3 | a0001c0003t0005g0141a0001c0003t0005g0164a0001c0003t0005g0240 | 3 | HG01261.hp2 HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.218-24187G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747032 | ||||||
| chr12:59747043
|
G | T | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-24176G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747043 | ||||||
| chr12:59747071
|
A | C | 1 | a0001c0001t0046g0002 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218-24148A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747071 | ||||||
| chr12:59747118
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-24101C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747118 | ||||||
| chr12:59747212
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-24007G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747212 | ||||||
| chr12:59747321
|
A | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.218-23898A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747321 | ||||||
| chr12:59747342
|
C | T | 3 | a0002c0002t0004g0040a0002c0002t0004g0256a0002c0002t0023g0238 | 3 | HG00099.hp1 HG00280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.218-23877C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747342 | ||||||
| chr12:59747625
|
C | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-23594C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747625 | ||||||
| chr12:59747712
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-23507C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747712 | ||||||
| chr12:59747737
|
T | G | 122 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.218-23482T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747737 | ||||||
| chr12:59747900
|
A | T | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218-23319A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747900 | ||||||
| chr12:59747926
|
C | T | 2 | a0001c0001t0001g0037a0002c0002t0008g0257 | 2 | HG01175.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.218-23293C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59747926 | ||||||
| chr12:59748167
|
G | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-23052G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748167 | ||||||
| chr12:59748318
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.218-22901G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748318 | ||||||
| chr12:59748410
|
A | G | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.218-22809A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748410 | ||||||
| chr12:59748434
|
A | G | 1 | a0001c0001t0047g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.218-22785A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748434 | ||||||
| chr12:59748461
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218-22758G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748461 | ||||||
| chr12:59748725
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-22494G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748725 | ||||||
| chr12:59748741
|
T | C | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-22478T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748741 | ||||||
| chr12:59748794
|
C | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-22425C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748794 | ||||||
| chr12:59748812
|
T | C | 7 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(4): Show | 7 | HG01175.hp1 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-22407T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748812 | ||||||
| chr12:59748816
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-22403T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748816 | ||||||
| chr12:59748987
|
C | T | 2 | a0003c0004t0009g0249a0003c0004t0009g0250 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.218-22232C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59748987 | ||||||
| chr12:59749211
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-22008T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749211 | ||||||
| chr12:59749286
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0028 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218-21933T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749286 | ||||||
| chr12:59749446
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-21773C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749446 | ||||||
| chr12:59749602
|
T | G | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-21617T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749602 | ||||||
| chr12:59749623
|
A | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-21596A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749623 | ||||||
| chr12:59749685
|
G | A | 133 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218-21534G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749685 | ||||||
| chr12:59749698
|
C | T | 1 | a0002c0002t0008g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218-21521C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749698 | ||||||
| chr12:59749771
|
C | G | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-21448C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749771 | ||||||
| chr12:59749790
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-21429G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749790 | ||||||
| chr12:59749809
|
T | A | 1 | a0001c0001t0002g0119 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.218-21410T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749809 | ||||||
| chr12:59749927
|
T | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-21292T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59749927 | ||||||
| chr12:59750017
|
G | T | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-21202G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750017 | ||||||
| chr12:59750171
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-21048T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750171 | ||||||
| chr12:59750259
|
A | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-20960A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750259 | ||||||
| chr12:59750360
|
A | G | 74 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.218-20859A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750360 | ||||||
| chr12:59750429
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-20790G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750429 | ||||||
| chr12:59750442
|
C | T | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-20777C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750442 | ||||||
| chr12:59750594
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20625A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750594 | ||||||
| chr12:59750603
|
C | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20616C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750603 | ||||||
| chr12:59750646
|
G | A | 10 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-20573G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750646 | ||||||
| chr12:59750669
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20550A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750669 | ||||||
| chr12:59750683
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.218-20536A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750683 | ||||||
| chr12:59750852
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20367C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750852 | ||||||
| chr12:59750871
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20348T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750871 | ||||||
| chr12:59750891
|
A | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20328A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750891 | ||||||
| chr12:59750916
|
A | G | 1 | a0001c0001t0007g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.218-20303A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750916 | ||||||
| chr12:59750969
|
C | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-20250C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59750969 | ||||||
| chr12:59751010
|
A | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-20209A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751010 | ||||||
| chr12:59751049
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-20170T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751049 | ||||||
| chr12:59751067
|
G | A | 7 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-20152G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751067 | ||||||
| chr12:59751177
|
G | A | 1 | a0001c0001t0019g0080 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.218-20042G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751177 | ||||||
| chr12:59751185
|
C | T | 10 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-20034C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751185 | ||||||
| chr12:59751270
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-19949C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751270 | ||||||
| chr12:59751281
|
C | T | 2 | a0001c0001t0035g0066a0002c0002t0008g0088 | 2 | HG00673.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.218-19938C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751281 | ||||||
| chr12:59751296
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-19923C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751296 | ||||||
| chr12:59751297
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-19922G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751297 | ||||||
| chr12:59751297
|
G | T | 11 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-19922G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751297 | ||||||
| chr12:59751314
|
G | A | 2 | a0001c0001t0007g0130a0001c0001t0007g0139 | 2 | HG02040.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.218-19905G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751314 | ||||||
| chr12:59751320
|
C | T | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-19899C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751320 | ||||||
| chr12:59751417
|
G | A | 32 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(29): Show | 32 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.218-19802G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751417 | ||||||
| chr12:59751419
|
T | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.218-19800T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751419 | ||||||
| chr12:59751441
|
A | G | 1 | a0001c0001t0025g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.218-19778A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751441 | ||||||
| chr12:59751478
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-19741C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751478 | ||||||
| chr12:59751744
|
A | G | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-19475A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751744 | ||||||
| chr12:59751819
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-19400C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751819 | ||||||
| chr12:59751948
|
C | T | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-19271C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751948 | ||||||
| chr12:59751956
|
C | T | 2 | a0002c0002t0003g0076a0002c0002t0003g0085 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.218-19263C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751956 | ||||||
| chr12:59751972
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-19247C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751972 | ||||||
| chr12:59751981
|
G | C | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-19238G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59751981 | ||||||
| chr12:59752162
|
C | CAG | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-19056_218-1905 others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59752162 | |||||
| chr12:59752251
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18968C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752251 | ||||||
| chr12:59752292
|
C | T | 25 | a0001c0001t0001g0155a0001c0001t0007g0020a0001c0001t0007g0031others(22): Show | 25 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.218-18927C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752292 | ||||||
| chr12:59752370
|
G | C | 1 | a0001c0001t0010g0123 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218-18849G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752370 | ||||||
| chr12:59752439
|
C | T | 1 | a0001c0001t0035g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218-18780C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752439 | ||||||
| chr12:59752451
|
G | A | 2 | a0002c0002t0003g0147a0002c0002t0003g0212 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.218-18768G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752451 | ||||||
| chr12:59752535
|
C | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-18684C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752535 | ||||||
| chr12:59752536
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18683A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752536 | ||||||
| chr12:59752573
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18646G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752573 | ||||||
| chr12:59752576
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18643G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752576 | ||||||
| chr12:59752614
|
C | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-18605C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752614 | ||||||
| chr12:59752625
|
C | G | 1 | a0001c0001t0026g0042 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.218-18594C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752625 | ||||||
| chr12:59752627
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18592C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752627 | ||||||
| chr12:59752729
|
C | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-18490C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752729 | ||||||
| chr12:59752735
|
G | C | 2 | a0001c0001t0015g0004a0001c0001t0015g0258 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.218-18484G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752735 | ||||||
| chr12:59752909
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.218-18310G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59752909 | ||||||
| chr12:59753005
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-18214G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753005 | ||||||
| chr12:59753092
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-18127C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753092 | ||||||
| chr12:59753130
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18089A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753130 | ||||||
| chr12:59753201
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0028 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218-18018C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753201 | ||||||
| chr12:59753211
|
A | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-18008A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753211 | ||||||
| chr12:59753286
|
C | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-17933C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753286 | ||||||
| chr12:59753363
|
T | C | 10 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-17856T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753363 | ||||||
| chr12:59753375
|
G | A | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-17844G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753375 | ||||||
| chr12:59753460
|
A | T | 111 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.218-17759A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753460 | ||||||
| chr12:59753621
|
A | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-17598A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753621 | ||||||
| chr12:59753624
|
C | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-17595C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753624 | ||||||
| chr12:59753697
|
C | T | 1 | a0001c0001t0007g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.218-17522C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753697 | ||||||
| chr12:59753698
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-17521G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753698 | ||||||
| chr12:59753752
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-17467A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753752 | ||||||
| chr12:59753793
|
C | G | 1 | a0002c0002t0003g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.218-17426C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753793 | ||||||
| chr12:59753861
|
G | T | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218-17358G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753861 | ||||||
| chr12:59753864
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-17355C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753864 | ||||||
| chr12:59753873
|
A | G | 36 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(33): Show | 36 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.218-17346A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753873 | ||||||
| chr12:59753898
|
C | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-17321C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753898 | ||||||
| chr12:59753943
|
T | A | 7 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(4): Show | 7 | HG01175.hp1 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-17276T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59753943 | ||||||
| chr12:59754058
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-17161T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754058 | ||||||
| chr12:59754318
|
G | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-16901G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754318 | ||||||
| chr12:59754332
|
A | G | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-16887A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754332 | ||||||
| chr12:59754346
|
T | A | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-16873T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754346 | ||||||
| chr12:59754350
|
A | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0028 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218-16869A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754350 | ||||||
| chr12:59754368
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218-16851A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754368 | ||||||
| chr12:59754385
|
G | C | 1 | a0001c0001t0015g0004 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218-16834G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754385 | ||||||
| chr12:59754423
|
A | G | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-16796A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754423 | ||||||
| chr12:59754426
|
T | A | 65 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.218-16793T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754426 | ||||||
| chr12:59754772
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-16447C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754772 | ||||||
| chr12:59754869
|
G | A | 7 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-16350G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754869 | ||||||
| chr12:59754883
|
C | G | 16 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-16336C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754883 | ||||||
| chr12:59754899
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-16320T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754899 | ||||||
| chr12:59754956
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-16263C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754956 | ||||||
| chr12:59754957
|
G | T | 40 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(37): Show | 40 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.218-16262G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754957 | ||||||
| chr12:59754972
|
T | G | 66 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.218-16247T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59754972 | ||||||
| chr12:59755071
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-16148A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755071 | ||||||
| chr12:59755192
|
C | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-16027C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755192 | ||||||
| chr12:59755208
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218-16011C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755208 | ||||||
| chr12:59755418
|
A | T | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218-15801A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755418 | ||||||
| chr12:59755430
|
C | T | 1 | a0001c0001t0020g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218-15789C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755430 | ||||||
| chr12:59755439
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0104 | 2 | NA18977.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.218-15780C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755439 | ||||||
| chr12:59755453
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-15766T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755453 | ||||||
| chr12:59755494
|
T | A | 20 | a0001c0001t0038g0062a0002c0002t0004g0036a0002c0002t0004g0038others(17): Show | 20 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.218-15725T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755494 | ||||||
| chr12:59755551
|
G | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-15668G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755551 | ||||||
| chr12:59755580
|
C | T | 6 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(3): Show | 6 | HG02257.hp1 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-15639C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755580 | ||||||
| chr12:59755657
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-15562G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755657 | ||||||
| chr12:59755662
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-15557A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755662 | ||||||
| chr12:59755669
|
T | C | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-15550T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755669 | ||||||
| chr12:59755672
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0041 | 3 | HG01123.hp2 NA18952.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.218-15547C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755672 | ||||||
| chr12:59755702
|
A | G | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-15517A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755702 | ||||||
| chr12:59755725
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-15494A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755725 | ||||||
| chr12:59755763
|
G | A | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-15456G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755763 | ||||||
| chr12:59755795
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-15424C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755795 | ||||||
| chr12:59755838
|
G | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-15381G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755838 | ||||||
| chr12:59755866
|
G | C | 1 | a0002c0002t0003g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.218-15353G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755866 | ||||||
| chr12:59755893
|
T | G | 1 | a0001c0001t0002g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.218-15326T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755893 | ||||||
| chr12:59755924
|
G | A | 141 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0051others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.218-15295G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755924 | ||||||
| chr12:59755948
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.218-15271C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755948 | ||||||
| chr12:59755977
|
G | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-15242G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59755977 | ||||||
| chr12:59756028
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-15191C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756028 | ||||||
| chr12:59756057
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.218-15162G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756057 | ||||||
| chr12:59756074
|
A | T | 2 | a0001c0001t0010g0123a0001c0003t0010g0019 | 2 | HG00639.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.218-15145A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756074 | ||||||
| chr12:59756088
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0028 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218-15131C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756088 | ||||||
| chr12:59756123
|
C | A | 25 | a0001c0001t0001g0155a0001c0001t0007g0020a0001c0001t0007g0031others(22): Show | 25 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.218-15096C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756123 | ||||||
| chr12:59756136
|
C | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218-15083C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756136 | ||||||
| chr12:59756221
|
C | CA | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14995dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59756221 | |||||
| chr12:59756303
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.218-14916A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756303 | ||||||
| chr12:59756349
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218-14870C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756349 | ||||||
| chr12:59756441
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14778A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756441 | ||||||
| chr12:59756442
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14777C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756442 | ||||||
| chr12:59756501
|
T | A | 36 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0048others(33): Show | 36 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.218-14718T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756501 | ||||||
| chr12:59756512
|
A | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218-14707A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756512 | ||||||
| chr12:59756513
|
C | T | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218-14706C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756513 | ||||||
| chr12:59756612
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14607G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756612 | ||||||
| chr12:59756635
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-14584G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756635 | ||||||
| chr12:59756636
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14583A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756636 | ||||||
| chr12:59756644
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14575C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756644 | ||||||
| chr12:59756688
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14531G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756688 | ||||||
| chr12:59756689
|
A | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14530A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756689 | ||||||
| chr12:59756698
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14521C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756698 | ||||||
| chr12:59756792
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14427A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756792 | ||||||
| chr12:59756811
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14408A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756811 | ||||||
| chr12:59756819
|
C | G | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-14400C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756819 | ||||||
| chr12:59756856
|
G | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14363G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756856 | ||||||
| chr12:59756899
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14320A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756899 | ||||||
| chr12:59756910
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14309A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756910 | ||||||
| chr12:59756927
|
T | TA | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-14286dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59756927 | |||||
| chr12:59756951
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14268T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756951 | ||||||
| chr12:59756983
|
A | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14236A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59756983 | ||||||
| chr12:59757000
|
T | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14219T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757000 | ||||||
| chr12:59757041
|
G | A | 1 | a0001c0003t0005g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.218-14178G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757041 | ||||||
| chr12:59757061
|
A | G | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14158A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757061 | ||||||
| chr12:59757113
|
G | T | 1 | a0001c0001t0015g0258 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-14106G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757113 | ||||||
| chr12:59757120
|
G | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-14099G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757120 | ||||||
| chr12:59757134
|
T | A | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-14085T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757134 | ||||||
| chr12:59757228
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-13991C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757228 | ||||||
| chr12:59757259
|
T | TAATAA | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-13942_218-1393 others(9): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59757259 | |||||
| chr12:59757308
|
C | G | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-13911C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757308 | ||||||
| chr12:59757403
|
A | T | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-13816A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757403 | ||||||
| chr12:59757561
|
C | A | 133 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.218-13658C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757561 | ||||||
| chr12:59757765
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-13454G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59757765 | ||||||
| chr12:59758243
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0002g0061a0001c0001t0044g0050 | 3 | HG00741.hp2 HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.218-12976G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758243 | ||||||
| chr12:59758444
|
G | A | 1 | a0001c0001t0007g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.218-12775G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758444 | ||||||
| chr12:59758519
|
A | G | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218-12700A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758519 | ||||||
| chr12:59758558
|
T | C | 2 | a0002c0002t0004g0201a0002c0002t0004g0219 | 2 | HG02055.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.218-12661T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758558 | ||||||
| chr12:59758886
|
G | A | 1 | a0006c0010t0020g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.218-12333G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758886 | ||||||
| chr12:59758888
|
G | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-12331G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59758888 | ||||||
| chr12:59759012
|
CT | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-12199delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59759012 | |||||
| chr12:59759040
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-12179T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759040 | ||||||
| chr12:59759086
|
C | T | 72 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-12133C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759086 | ||||||
| chr12:59759152
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.218-12067A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759152 | ||||||
| chr12:59759202
|
A | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-12017A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759202 | ||||||
| chr12:59759236
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-11983A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759236 | ||||||
| chr12:59759427
|
G | A | 1 | a0001c0001t0007g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218-11792G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759427 | ||||||
| chr12:59759515
|
G | A | 15 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(12): Show | 15 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.218-11704G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759515 | ||||||
| chr12:59759708
|
A | C | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218-11511A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759708 | ||||||
| chr12:59759781
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-11438C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759781 | ||||||
| chr12:59759950
|
C | G | 7 | a0002c0002t0008g0072a0002c0002t0008g0088a0002c0002t0008g0206others(4): Show | 7 | HG01175.hp1 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-11269C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759950 | ||||||
| chr12:59759983
|
A | G | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.218-11236A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59759983 | ||||||
| chr12:59760117
|
C | T | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-11102C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760117 | ||||||
| chr12:59760256
|
G | A | 37 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(34): Show | 37 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.218-10963G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760256 | ||||||
| chr12:59760272
|
G | T | 64 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.218-10947G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760272 | ||||||
| chr12:59760443
|
T | A | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-10776T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760443 | ||||||
| chr12:59760539
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-10680A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760539 | ||||||
| chr12:59760649
|
A | T | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-10570A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760649 | ||||||
| chr12:59760831
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.218-10388T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59760831 | ||||||
| chr12:59761513
|
C | T | 1 | a0001c0001t0035g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218-9706C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59761513 | ||||||
| chr12:59761690
|
A | G | 16 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(13): Show | 16 | HG00621.hp1 HG01261.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.218-9529A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59761690 | ||||||
| chr12:59761996
|
T | A | 1 | a0001c0001t0002g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.218-9223T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59761996 | ||||||
| chr12:59762103
|
G | C | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.218-9116G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762103 | ||||||
| chr12:59762137
|
G | C | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218-9082G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762137 | ||||||
| chr12:59762265
|
T | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-8954T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762265 | ||||||
| chr12:59762333
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-8886C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762333 | ||||||
| chr12:59762334
|
G | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-8885G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762334 | ||||||
| chr12:59762339
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-8880G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762339 | ||||||
| chr12:59762351
|
G | A | 1 | a0002c0002t0004g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.218-8868G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762351 | ||||||
| chr12:59762422
|
G | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-8797G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762422 | ||||||
| chr12:59762425
|
CT | C | 7 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-8792delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59762425 | |||||
| chr12:59762492
|
C | T | 1 | a0001c0001t0035g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218-8727C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762492 | ||||||
| chr12:59762509
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.218-8710G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762509 | ||||||
| chr12:59762521
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218-8698T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762521 | ||||||
| chr12:59762675
|
C | T | 1 | a0001c0001t0042g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218-8544C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762675 | ||||||
| chr12:59762774
|
C | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-8445C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762774 | ||||||
| chr12:59762808
|
G | A | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-8411G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762808 | ||||||
| chr12:59762822
|
C | CA | 40 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 40 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.218-8384dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59762822 | |||||
| chr12:59762840
|
A | AC | 65 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.218-8379_218-8378i others(3): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762840 | ||||||
| chr12:59762915
|
T | A | 1 | a0001c0001t0002g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.218-8304T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762915 | ||||||
| chr12:59762966
|
G | A | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-8253G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59762966 | ||||||
| chr12:59763073
|
A | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-8146A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763073 | ||||||
| chr12:59763152
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-8067T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763152 | ||||||
| chr12:59763217
|
A | G | 3 | a0002c0002t0004g0040a0002c0002t0004g0256a0002c0002t0023g0238 | 3 | HG00099.hp1 HG00280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.218-8002A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763217 | ||||||
| chr12:59763291
|
G | T | 1 | a0002c0002t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-7928G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763291 | ||||||
| chr12:59763346
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218-7873A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763346 | ||||||
| chr12:59763480
|
A | G | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-7739A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763480 | ||||||
| chr12:59763608
|
A | G | 8 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0025g0248others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-7611A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763608 | ||||||
| chr12:59763744
|
C | T | 1 | a0001c0003t0005g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218-7475C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763744 | ||||||
| chr12:59763771
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-7448G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763771 | ||||||
| chr12:59763867
|
G | T | 1 | a0002c0002t0003g0107 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.218-7352G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763867 | ||||||
| chr12:59763938
|
C | G | 4 | a0001c0001t0002g0101a0001c0001t0002g0160a0001c0001t0002g0161others(1): Show | 4 | HG00597.hp2 NA18940.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-7281C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763938 | ||||||
| chr12:59763944
|
C | T | 1 | a0001c0001t0007g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-7275C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59763944 | ||||||
| chr12:59764088
|
C | A | 4 | a0002c0002t0008g0206a0002c0002t0008g0227a0002c0002t0008g0251others(1): Show | 4 | HG02976.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-7131C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764088 | ||||||
| chr12:59764358
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-6861T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764358 | ||||||
| chr12:59764427
|
G | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-6792G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764427 | ||||||
| chr12:59764481
|
C | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-6738C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764481 | ||||||
| chr12:59764490
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-6729C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764490 | ||||||
| chr12:59764504
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218-6715C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764504 | ||||||
| chr12:59764506
|
C | T | 1 | a0001c0001t0010g0035 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.218-6713C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764506 | ||||||
| chr12:59764563
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.218-6656G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764563 | ||||||
| chr12:59764588
|
T | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-6631T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764588 | ||||||
| chr12:59764717
|
T | G | 2 | a0002c0002t0003g0191a0008c0007t0003g0045 | 2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.218-6502T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764717 | ||||||
| chr12:59764752
|
T | C | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.218-6467T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59764752 | ||||||
| chr12:59765197
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-6022A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765197 | ||||||
| chr12:59765274
|
C | T | 2 | a0001c0003t0005g0074a0001c0003t0005g0075 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.218-5945C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765274 | ||||||
| chr12:59765307
|
G | C | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.218-5912G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765307 | ||||||
| chr12:59765371
|
C | T | 3 | a0001c0003t0005g0087a0001c0003t0005g0091a0001c0003t0005g0216 | 3 | HG00621.hp1 NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.218-5848C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765371 | ||||||
| chr12:59765501
|
A | T | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-5718A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765501 | ||||||
| chr12:59765561
|
T | G | 1 | a0001c0001t0002g0057 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.218-5658T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765561 | ||||||
| chr12:59765662
|
T | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-5557T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765662 | ||||||
| chr12:59765677
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.218-5542G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765677 | ||||||
| chr12:59765713
|
T | C | 1 | a0001c0001t0002g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218-5506T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765713 | ||||||
| chr12:59765719
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218-5500C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765719 | ||||||
| chr12:59765764
|
C | T | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-5455C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765764 | ||||||
| chr12:59765875
|
A | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-5344A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765875 | ||||||
| chr12:59765887
|
G | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-5332G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765887 | ||||||
| chr12:59765942
|
A | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218-5277A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765942 | ||||||
| chr12:59765974
|
G | C | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-5245G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765974 | ||||||
| chr12:59765994
|
C | A | 1 | a0001c0001t0026g0042 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.218-5225C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59765994 | ||||||
| chr12:59766007
|
C | A | 9 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-5212C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766007 | ||||||
| chr12:59766070
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0119 | 2 | HG02155.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.218-5149T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766070 | ||||||
| chr12:59766296
|
T | C | 1 | a0002c0002t0004g0038 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.218-4923T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766296 | ||||||
| chr12:59766410
|
G | A | 72 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-4809G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766410 | ||||||
| chr12:59766415
|
T | C | 21 | a0001c0001t0007g0064a0001c0001t0043g0047a0001c0001t0048g0081others(18): Show | 21 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.218-4804T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766415 | ||||||
| chr12:59766423
|
A | C | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-4796A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766423 | ||||||
| chr12:59766445
|
C | T | 40 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(37): Show | 40 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.218-4774C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766445 | ||||||
| chr12:59766630
|
C | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-4589C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766630 | ||||||
| chr12:59766647
|
A | G | 1 | a0001c0001t0011g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218-4572A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766647 | ||||||
| chr12:59766665
|
A | C | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-4554A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766665 | ||||||
| chr12:59766673
|
C | G | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218-4546C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766673 | ||||||
| chr12:59766718
|
C | G | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.218-4501C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766718 | ||||||
| chr12:59766760
|
G | A | 19 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.218-4459G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766760 | ||||||
| chr12:59766763
|
G | T | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-4456G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59766763 | ||||||
| chr12:59767061
|
AG | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-4155delG | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59767061 | |||||
| chr12:59767225
|
C | A | 73 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-3994C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767225 | ||||||
| chr12:59767389
|
A | G | 2 | a0001c0003t0005g0093a0001c0003t0005g0236 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.218-3830A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767389 | ||||||
| chr12:59767669
|
G | C | 1 | a0001c0001t0039g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.218-3550G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767669 | ||||||
| chr12:59767837
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-3382G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767837 | ||||||
| chr12:59767943
|
T | TG | 5 | a0001c0001t0007g0031a0001c0001t0007g0064a0001c0001t0007g0070others(2): Show | 5 | HG01358.hp2 HG01928.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-3272dupG | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59767943 | |||||
| chr12:59767948
|
T | G | 12 | a0001c0001t0007g0020a0001c0001t0007g0031a0001c0001t0007g0052others(9): Show | 12 | HG00673.hp1 HG00735.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-3271T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767948 | ||||||
| chr12:59767956
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.218-3263A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59767956 | ||||||
| chr12:59768058
|
G | A | 1 | a0001c0003t0005g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.218-3161G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768058 | ||||||
| chr12:59768128
|
G | A | 1 | a0002c0002t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.218-3091G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768128 | ||||||
| chr12:59768129
|
C | A | 1 | a0002c0002t0003g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.218-3090C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768129 | ||||||
| chr12:59768160
|
G | GA | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-3055dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59768160 | |||||
| chr12:59768758
|
A | G | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218-2461A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768758 | ||||||
| chr12:59768826
|
G | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-2393G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768826 | ||||||
| chr12:59768916
|
C | T | 72 | a0001c0001t0002g0224a0002c0002t0003g0008a0002c0002t0003g0060others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.218-2303C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59768916 | ||||||
| chr12:59769046
|
GC | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-2171delC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59769046 | |||||
| chr12:59769088
|
C | T | 1 | a0001c0003t0005g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218-2131C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59769088 | ||||||
| chr12:59769296
|
C | G | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.218-1923C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59769296 | ||||||
| chr12:59769368
|
T | C | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-1851T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59769368 | ||||||
| chr12:59769387
|
C | G | 1 | a0001c0001t0007g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.218-1832C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59769387 | ||||||
| chr12:59769921
|
A | G | 4 | a0002c0002t0004g0036a0002c0002t0004g0136a0002c0002t0004g0137others(1): Show | 4 | NA18940.hp2 NA18957.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-1298A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59769921 | ||||||
| chr12:59770035
|
A | G | 73 | a0001c0001t0002g0224a0001c0001t0038g0062a0002c0002t0003g0008others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218-1184A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770035 | ||||||
| chr12:59770266
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-953A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770266 | ||||||
| chr12:59770422
|
C | T | 1 | a0001c0003t0005g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.218-797C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770422 | ||||||
| chr12:59770434
|
C | T | 2 | a0001c0001t0045g0013a0001c0001t0046g0002 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.218-785C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770434 | ||||||
| chr12:59770443
|
A | G | 1 | a0002c0002t0004g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.218-776A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770443 | ||||||
| chr12:59770622
|
G | A | 3 | a0002c0002t0004g0214a0002c0002t0004g0217a0002c0002t0004g0231 | 3 | HG01358.hp1 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.218-597G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770622 | ||||||
| chr12:59770627
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-592T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770627 | ||||||
| chr12:59770804
|
A | G | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-415A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770804 | ||||||
| chr12:59770892
|
C | T | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-327C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59770892 | ||||||
| chr12:59770999
|
TTTA | T | 31 | a0002c0002t0003g0060a0002c0002t0003g0094a0002c0002t0003g0100others(28): Show | 31 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.218-214_218-212del others(3): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 59770999 | |||||
| chr12:59771083
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-136A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59771083 | ||||||
| chr12:59771174
|
A | G | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.218-45A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 3/5 | chr12 | 59771174 | ||||||
| chr12:59771490
|
A | G | 135 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.361+128A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59771490 | ||||||
| chr12:59771635
|
G | C | 1 | a0002c0002t0003g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361+273G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59771635 | ||||||
| chr12:59771642
|
T | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.361+280T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59771642 | ||||||
| chr12:59771937
|
C | A | 1 | a0001c0001t0011g0024 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.361+575C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59771937 | ||||||
| chr12:59772087
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.361+725G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772087 | ||||||
| chr12:59772113
|
T | C | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.361+751T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772113 | ||||||
| chr12:59772210
|
C | A | 122 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.361+848C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772210 | ||||||
| chr12:59772375
|
A | G | 1 | a0002c0002t0003g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.361+1013A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772375 | ||||||
| chr12:59772445
|
T | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.361+1083T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772445 | ||||||
| chr12:59772533
|
CAA | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.361+1173_361+1174d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 59772533 | |||||
| chr12:59772640
|
T | C | 123 | a0001c0001t0002g0224a0001c0001t0006g0001a0001c0001t0006g0029others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.361+1278T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772640 | ||||||
| chr12:59772758
|
C | T | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.361+1396C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59772758 | ||||||
| chr12:59773072
|
C | T | 20 | a0001c0001t0043g0047a0001c0001t0048g0081a0001c0003t0005g0007others(17): Show | 20 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.362-1585C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773072 | ||||||
| chr12:59773092
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.362-1565T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773092 | ||||||
| chr12:59773104
|
T | TA | 5 | a0001c0001t0001g0155a0001c0001t0007g0128a0001c0001t0028g0133others(2): Show | 5 | HG00735.hp2 HG01175.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-1540dupA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 59773104 | |||||
| chr12:59773146
|
T | C | 3 | a0002c0002t0008g0206a0002c0002t0008g0227a0002c0002t0008g0251 | 3 | HG02976.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362-1511T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773146 | ||||||
| chr12:59773150
|
A | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.362-1507A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773150 | ||||||
| chr12:59773347
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-1310T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773347 | ||||||
| chr12:59773423
|
C | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-1234C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773423 | ||||||
| chr12:59773442
|
CTAGG | C | 18 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.362-1212_362-1209d others(6): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 59773442 | |||||
| chr12:59773570
|
C | CTT | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-1075_362-1074d others(4): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 59773570 | |||||
| chr12:59773621
|
G | GAGCCTGG others(1): Show |
11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-1036_362-1035i others(10): Show |
SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773621 | ||||||
| chr12:59773623
|
G | T | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-1034G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773623 | ||||||
| chr12:59773651
|
G | A | 1 | a0002c0002t0004g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.362-1006G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773651 | ||||||
| chr12:59773687
|
A | C | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-970A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773687 | ||||||
| chr12:59773726
|
G | A | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.362-931G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773726 | ||||||
| chr12:59773751
|
G | C | 16 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.362-906G>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773751 | ||||||
| chr12:59773784
|
C | T | 12 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0001t0013g0069others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.362-873C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773784 | ||||||
| chr12:59773873
|
T | C | 1 | a0001c0001t0018g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.362-784T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773873 | ||||||
| chr12:59773960
|
C | T | 1 | a0001c0001t0026g0042 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.362-697C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59773960 | ||||||
| chr12:59774054
|
C | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-603C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59774054 | ||||||
| chr12:59774103
|
C | A | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-554C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59774103 | ||||||
| chr12:59774418
|
C | T | 19 | a0001c0001t0048g0081a0001c0003t0005g0007a0001c0003t0005g0009others(16): Show | 19 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-239C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 4/5 | chr12 | 59774418 | ||||||
| chr12:59775484
|
G | A | 32 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(29): Show | 32 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1180+9G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775484 | ||||||
| chr12:59775530
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1180+55C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775530 | ||||||
| chr12:59775540
|
A | T | 2 | a0004c0005t0009g0089a0004c0005t0009g0233 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1180+65A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775540 | ||||||
| chr12:59775747
|
C | G | 1 | a0002c0002t0003g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1180+272C>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775747 | ||||||
| chr12:59775881
|
A | AT | 6 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180+412dupT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 59775881 | |||||
| chr12:59775942
|
A | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1180+467A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775942 | ||||||
| chr12:59775981
|
T | C | 1 | a0001c0001t0006g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1180+506T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59775981 | ||||||
| chr12:59776025
|
T | A | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180+550T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59776025 | ||||||
| chr12:59776521
|
T | C | 7 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+1046T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59776521 | ||||||
| chr12:59776757
|
C | T | 2 | a0001c0003t0005g0087a0001c0003t0005g0091 | 2 | NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1180+1282C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59776757 | ||||||
| chr12:59777026
|
G | A | 2 | a0001c0001t0013g0069a0001c0001t0013g0259 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1180+1551G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777026 | ||||||
| chr12:59777164
|
T | A | 1 | a0001c0003t0005g0087 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1180+1689T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777164 | ||||||
| chr12:59777347
|
T | G | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1180+1872T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777347 | ||||||
| chr12:59777355
|
G | A | 2 | a0001c0001t0041g0232a0001c0001t0048g0081 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1180+1880G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777355 | ||||||
| chr12:59777432
|
T | C | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1180+1957T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777432 | ||||||
| chr12:59777671
|
A | G | 1 | a0001c0001t0043g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1181-1752A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777671 | ||||||
| chr12:59777700
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1181-1723T>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777700 | ||||||
| chr12:59777706
|
G | A | 1 | a0002c0002t0003g0111 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1181-1717G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777706 | ||||||
| chr12:59777718
|
A | G | 18 | a0001c0003t0005g0007a0001c0003t0005g0009a0001c0003t0005g0012others(15): Show | 18 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1181-1705A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777718 | ||||||
| chr12:59777747
|
T | C | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181-1676T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777747 | ||||||
| chr12:59777803
|
T | TC | 42 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0041others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1181-1614dupC | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 59777803 | |||||
| chr12:59777838
|
T | G | 71 | a0001c0001t0038g0062a0002c0002t0003g0008a0002c0002t0003g0060others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1181-1585T>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777838 | ||||||
| chr12:59777839
|
T | C | 1 | a0002c0002t0003g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1181-1584T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777839 | ||||||
| chr12:59777873
|
A | G | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1181-1550A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777873 | ||||||
| chr12:59777893
|
A | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1181-1530A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777893 | ||||||
| chr12:59777907
|
G | T | 1 | a0002c0006t0022g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1181-1516G>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777907 | ||||||
| chr12:59777933
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1181-1490G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777933 | ||||||
| chr12:59777975
|
C | T | 1 | a0001c0001t0013g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1181-1448C>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59777975 | ||||||
| chr12:59778102
|
G | A | 1 | a0001c0001t0041g0232 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1181-1321G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59778102 | ||||||
| chr12:59778196
|
A | G | 2 | a0001c0001t0018g0005a0001c0001t0018g0096 | 2 | NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1181-1227A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59778196 | ||||||
| chr12:59778692
|
CT | C | 71 | a0002c0002t0003g0008a0002c0002t0003g0060a0002c0002t0003g0076others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1181-729delT | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 59778692 | |||||
| chr12:59778751
|
C | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1181-672C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59778751 | ||||||
| chr12:59778790
|
A | T | 1 | a0002c0002t0003g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1181-633A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59778790 | ||||||
| chr12:59778977
|
C | A | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1181-446C>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59778977 | ||||||
| chr12:59779024
|
A | G | 1 | a0001c0001t0048g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1181-399A>G | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59779024 | ||||||
| chr12:59779046
|
G | A | 1 | a0002c0002t0008g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1181-377G>A | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59779046 | ||||||
| chr12:59779151
|
CA | C | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181-266delA | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 59779151 | |||||
| chr12:59779153
|
A | C | 19 | a0001c0001t0006g0001a0001c0001t0006g0029a0001c0001t0006g0117others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1181-270A>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59779153 | ||||||
| chr12:59779271
|
A | T | 11 | a0001c0001t0012g0166a0001c0001t0012g0246a0001c0001t0012g0247others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181-152A>T | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59779271 | ||||||
| chr12:59779290
|
T | C | 1 | a0007c0008t0040g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1181-133T>C | SLC16A7 | ENSG00000118596.12 | transcript | ENST00000547379.6 | protein_coding | 5/5 | chr12 | 59779290 |