Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22828 |
|---|---|
| ensemblid | ENSG00000213079.10 |
| hgncid | 20959 |
| symbol | SCAF8 |
| name | SR-related CTD associated factor 8 |
| refseq_nuc | NM_014892.5 |
| refseq_prot | NP_055707.3 |
| ensembl_nuc | ENST00000367178.8 |
| ensembl_prot | ENSP00000356146.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 154733416 |
| end | 154834221 |
| strand | + |
| ver | v1.2 |
| region | chr6:154733416-154834221 |
| region5000 | chr6:154728416-154839221 |
| regionname0 | SCAF8_chr6_154733416_154834221 |
| regionname5000 | SCAF8_chr6_154728416_154839221 |
| 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 | 1271 | 270 | 79 | 62 | 86 | 11 | 30 | 52 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0002 | 0/0 | 1271 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0003 | 0/0 | 1271 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0004 | 0/0 | 1271 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0005 | 0/0 | 1271 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0006 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0007 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| 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 | 1/0 | 3816 | 256 | 74 | 57 | 85 | 11 | 28 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0002 | 0/0 | 3816 | 6 | 0 | 5 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0003 | 0/0 | 3816 | 3 | 3 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0004 | 0/0 | 3816 | 3 | 2 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0005 | 0/0 | 3816 | 2 | 1 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0006 | 0/0 | 3816 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0007 | 0/0 | 3816 | 2 | 1 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0008 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0009 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0010 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0011 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0012 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0013 | 0/0 | 3816 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0014 | 0/1 | 3816 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| c0015 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1312 | 172 | 51 | 24 | 67 | 8 | 21 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0002 | 0/1 | 1312 | 84 | 26 | 29 | 18 | 3 | 7 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0003 | 0/0 | 1312 | 9 | 8 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0004 | 0/0 | 1313 | 8 | 0 | 7 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0005 | 0/0 | 1312 | 3 | 0 | 0 | 0 | 0 | 3 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0006 | 0/0 | 1298 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0007 | 0/0 | 1312 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0008 | 0/0 | 1312 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0009 | 0/0 | 1300 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| t0010 | 0/0 | 1313 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| 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 | 1/0 | 3816 | 256 | 74 | 57 | 85 | 11 | 28 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0002 | 0/0 | 3816 | 6 | 0 | 5 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0006 | 0/0 | 3816 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0008 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0011 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0012 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0013 | 0/0 | 3816 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0014 | 0/1 | 3816 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0015 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0002c0004 | 0/0 | 3816 | 3 | 2 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0003c0003 | 0/0 | 3816 | 3 | 3 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0004c0007 | 0/0 | 3816 | 2 | 1 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0005c0005 | 0/0 | 3816 | 2 | 1 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0006c0009 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0007c0010 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5127 | 161 | 45 | 24 | 64 | 8 | 19 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0002 | 0/0 | 5127 | 69 | 20 | 24 | 18 | 2 | 5 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0003 | 0/0 | 5127 | 9 | 8 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0004 | 0/0 | 5128 | 8 | 0 | 7 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0005 | 0/0 | 5127 | 3 | 0 | 0 | 0 | 0 | 3 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0006 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0007 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0008 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0009 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0001t0010 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0002t0002 | 0/0 | 5127 | 6 | 0 | 5 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0006t0001 | 0/0 | 5127 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0008t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0011t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0012t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0013t0002 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0014t0002 | 0/1 | 5127 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0001c0015t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0002c0004t0001 | 0/0 | 5127 | 3 | 2 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0003c0003t0002 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0004c0007t0001 | 0/0 | 5127 | 2 | 1 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0005c0005t0002 | 0/0 | 5127 | 2 | 1 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0006c0009t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| a0007c0010t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | copy fasta | chr6 | 154728416 | 154839221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0009g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0008t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0012t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0013t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0014t0002g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0015t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0004c0007t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0004c0007t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0005c0005t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0005c0005t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0006c0009t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0007c0010t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0249 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0088 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01891 | hp2 | a0001 | c0012 | t0002 | g0279 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02071 | hp2 | a0001 | c0015 | t0001 | g0114 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02145 | hp1 | a0002 | c0004 | t0001 | g0186 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02257 | hp1 | a0004 | c0007 | t0001 | g0177 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0254 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0253 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0187 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02886 | hp1 | a0005 | c0005 | t0002 | g0256 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0152 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0223 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0274 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0273 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03540 | hp1 | a0001 | c0008 | t0002 | g0257 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03710 | hp2 | a0001 | c0013 | t0002 | g0106 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03834 | hp1 | a0004 | c0007 | t0001 | g0144 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0196 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0209 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0188 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0156 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18994 | hp1 | a0006 | c0009 | t0001 | g0128 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0272 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19088 | hp2 | a0007 | c0010 | t0001 | g0100 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ASW | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20752 | hp2 | a0005 | c0005 | t0002 | g0255 | EUR | TSI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA21309 | hp2 | a0001 | c0011 | t0001 | g0208 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0014 | t0002 | g0052 | REF | REF | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0030 | REF | REF | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154808146
|
A | T | 1 | a0004 | 2 | HG02257.hp1 HG03834.hp1 |
missense_variant | MODERATE | c.1058A>T | p.Gln353Leu | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/20 | 1543/5127 | 1058/3816 | 353/1271 | chr6 | 154808146 | ||
| chr6:154822368
|
A | G | 1 | a0002 | 3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1885A>G | p.Thr629Ala | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/20 | 2370/5127 | 1885/3816 | 629/1271 | chr6 | 154822368 | ||
| chr6:154832173
|
G | A | 1 | a0005 | 2 | HG02886.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.2594G>A | p.Ser865Asn | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3079/5127 | 2594/3816 | 865/1271 | chr6 | 154832173 | ||
| chr6:154832706
|
A | G | 1 | a0007 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.3127A>G | p.Ile1043Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3612/5127 | 3127/3816 | 1043/1271 | chr6 | 154832706 | ||
| chr6:154832982
|
G | A | 1 | a0006 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.3403G>A | p.Gly1135Ser | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3888/5127 | 3403/3816 | 1135/1271 | chr6 | 154832982 | ||
| chr6:154833096
|
A | G | 1 | a0003 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.3517A>G | p.Met1173Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 4002/5127 | 3517/3816 | 1173/1271 | chr6 | 154833096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154787917
|
A | G | 1 | a0001c0015 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.216A>G | p.Gln72Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/20 | 701/5127 | 216/3816 | 72/1271 | chr6 | 154787917 | ||
| chr6:154802138
|
C | G | 1 | a0001c0014 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.774C>G | p.Ser258Ser | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/20 | 1259/5127 | 774/3816 | 258/1271 | chr6 | 154802138 | ||
| chr6:154808198
|
A | G | 1 | a0001c0006 | 2 | HG02257.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.1110A>G | p.Gln370Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/20 | 1595/5127 | 1110/3816 | 370/1271 | chr6 | 154808198 | ||
| chr6:154818577
|
G | T | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1620G>T | p.Gly540Gly | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/20 | 2105/5127 | 1620/3816 | 540/1271 | chr6 | 154818577 | ||
| chr6:154820179
|
C | T | 1 | a0001c0002 | 6 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1638C>T | p.Ile546Ile | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2123/5127 | 1638/3816 | 546/1271 | chr6 | 154820179 | ||
| chr6:154820248
|
A | G | 1 | a0001c0012 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1707A>G | p.Thr569Thr | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2192/5127 | 1707/3816 | 569/1271 | chr6 | 154820248 | ||
| chr6:154820332
|
T | C | 1 | a0001c0008 | 1 | HG03540.hp1 | splice_region_variant&synonymous_variant | LOW | c.1791T>C | p.Thr597Thr | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2276/5127 | 1791/3816 | 597/1271 | chr6 | 154820332 | ||
| chr6:154824368
|
A | G | 1 | a0001c0011 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2061A>G | p.Gln687Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/20 | 2546/5127 | 2061/3816 | 687/1271 | chr6 | 154824368 | ||
| chr6:154831997
|
G | A | 1 | a0005c0005 | 2 | HG02886.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.2418G>A | p.Val806Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 2903/5127 | 2418/3816 | 806/1271 | chr6 | 154831997 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154733530
|
G | A | 1 | a0001c0001t0005 | 3 | HG03017.hp1 HG03942.hp1 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-371G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 371 | chr6 | 154733530 | |||||
| chr6:154733559
|
AGGGGCTA others(7): Show |
A | 1 | a0001c0001t0006 | 2 | NA18994.hp2 NA19065.hp1 |
5_prime_UTR_variant | MODIFIER | c.-337_-324delCTAGAG others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 324 | INFO_REALIGN_3_PRIME | chr6 | 154733559 | ||||
| chr6:154733681
|
T | C | 1 | a0001c0001t0003 | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-220T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 220 | chr6 | 154733681 | |||||
| chr6:154733742
|
G | A | 1 | a0001c0001t0007 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 159 | chr6 | 154733742 | |||||
| chr6:154733815
|
G | A | 1 | a0001c0001t0008 | 1 | NA18987.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 86 | chr6 | 154733815 | |||||
| chr6:154733854
|
GCCGCCGC others(5): Show |
G | 1 | a0001c0001t0009 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38_-27delTCTTCCGC others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 27 | INFO_REALIGN_3_PRIME | chr6 | 154733854 | ||||
| chr6:154833581
|
A | G | 1 | a0001c0001t0010 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 186 | chr6 | 154833581 | |||||
| chr6:154833905
|
C | T | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(8): Show | 96 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*510C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 510 | chr6 | 154833905 | |||||
| chr6:154833961
|
T | TA | 2 | a0001c0001t0004a0001c0001t0010 | 9 | HG00099.hp1 HG01081.hp1 HG01255.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*572dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 573 | INFO_REALIGN_3_PRIME | chr6 | 154833961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154734183
|
C | T | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+253C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734183 | ||||||
| chr6:154734185
|
A | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+255A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734185 | ||||||
| chr6:154734189
|
C | T | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+259C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734189 | ||||||
| chr6:154734227
|
C | G | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+297C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734227 | ||||||
| chr6:154734232
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+302C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734232 | ||||||
| chr6:154734287
|
C | T | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734287 | ||||||
| chr6:154734301
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.30+371A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734301 | ||||||
| chr6:154734403
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+473G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734403 | ||||||
| chr6:154734419
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | NA18960.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.30+489G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734419 | ||||||
| chr6:154734470
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+540G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734470 | ||||||
| chr6:154734615
|
C | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.30+685C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734615 | ||||||
| chr6:154734622
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.30+692C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734622 | ||||||
| chr6:154734993
|
A | G | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1063A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734993 | ||||||
| chr6:154735024
|
T | C | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+1094T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735024 | ||||||
| chr6:154735035
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.30+1105A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735035 | ||||||
| chr6:154735038
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1108C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735038 | ||||||
| chr6:154735108
|
AG | A | 3 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG00438.hp1 HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.30+1179delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735108 | ||||||
| chr6:154735120
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+1190T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735120 | ||||||
| chr6:154735123
|
A | C | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+1193A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735123 | ||||||
| chr6:154735124
|
C | CA | 13 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+1208dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735124 | |||||
| chr6:154735206
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1276A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735206 | ||||||
| chr6:154735402
|
T | C | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+1472T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735402 | ||||||
| chr6:154735422
|
A | G | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+1492A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735422 | ||||||
| chr6:154735519
|
C | CT | 136 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(133): Show | 136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.30+1605dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735519 | |||||
| chr6:154735519
|
C | CTT | 70 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0198others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.30+1604_30+1605dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735519 | |||||
| chr6:154735554
|
T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1624T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735554 | ||||||
| chr6:154735575
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+1645A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735575 | ||||||
| chr6:154735726
|
C | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+1796C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735726 | ||||||
| chr6:154735908
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01070.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.30+1978C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735908 | ||||||
| chr6:154735915
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0189a0002c0004t0001g0186others(2): Show | 5 | HG02145.hp1 HG02735.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1985C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735915 | ||||||
| chr6:154735919
|
C | T | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1989C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735919 | ||||||
| chr6:154735986
|
T | C | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+2056T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735986 | ||||||
| chr6:154736176
|
A | AC | 22 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0001g0096others(19): Show | 22 | HG00621.hp2 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+2249dupC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736176 | |||||
| chr6:154736180
|
T | C | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+2250T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736180 | ||||||
| chr6:154736265
|
C | CT | 168 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.30+2356dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | |||||
| chr6:154736265
|
C | CTT | 30 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0173others(27): Show | 30 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.30+2355_30+2356dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | |||||
| chr6:154736265
|
CT | C | 8 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(5): Show | 8 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+2356delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | |||||
| chr6:154736265
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+2345_30+2356del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | |||||
| chr6:154736346
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+2416A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736346 | ||||||
| chr6:154736394
|
C | T | 6 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+2464C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736394 | ||||||
| chr6:154736518
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.30+2588C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736518 | ||||||
| chr6:154736563
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+2633C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736563 | ||||||
| chr6:154736634
|
A | G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+2704A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736634 | ||||||
| chr6:154736738
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+2808C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736738 | ||||||
| chr6:154736740
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+2810G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736740 | ||||||
| chr6:154736773
|
T | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+2843T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736773 | ||||||
| chr6:154736788
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.30+2858T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736788 | ||||||
| chr6:154736849
|
CTTAT | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0113a0001c0015t0001g0114 | 3 | HG00408.hp1 HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.30+2928_30+2931del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736849 | |||||
| chr6:154736953
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+3023A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736953 | ||||||
| chr6:154736974
|
T | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+3044T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736974 | ||||||
| chr6:154737097
|
G | T | 13 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(10): Show | 13 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+3167G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737097 | ||||||
| chr6:154737285
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+3355A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737285 | ||||||
| chr6:154737323
|
TAGCTCTA others(9): Show |
T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+3396_30+3411del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154737323 | |||||
| chr6:154737403
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.30+3473C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737403 | ||||||
| chr6:154737427
|
T | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+3497T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737427 | ||||||
| chr6:154737504
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+3574C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737504 | ||||||
| chr6:154737536
|
T | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+3606T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737536 | ||||||
| chr6:154737573
|
A | T | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+3643A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737573 | ||||||
| chr6:154737663
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.30+3733C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737663 | ||||||
| chr6:154737711
|
G | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+3781G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737711 | ||||||
| chr6:154737805
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.30+3875A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737805 | ||||||
| chr6:154737813
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.30+3883G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737813 | ||||||
| chr6:154737885
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+3955A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737885 | ||||||
| chr6:154737916
|
T | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02602.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3986T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737916 | ||||||
| chr6:154737945
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4015C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737945 | ||||||
| chr6:154738106
|
G | T | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.30+4176G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738106 | ||||||
| chr6:154738165
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+4235T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738165 | ||||||
| chr6:154738210
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+4280G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738210 | ||||||
| chr6:154738291
|
A | C | 1 | a0001c0001t0004g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.30+4361A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738291 | ||||||
| chr6:154738304
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.30+4374G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738304 | ||||||
| chr6:154738580
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+4650G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738580 | ||||||
| chr6:154738606
|
A | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+4676A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738606 | ||||||
| chr6:154738714
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.30+4784A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738714 | ||||||
| chr6:154738880
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.30+4950A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738880 | ||||||
| chr6:154738995
|
G | T | 3 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG00438.hp1 HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.30+5065G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738995 | ||||||
| chr6:154739001
|
A | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+5071A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739001 | ||||||
| chr6:154739033
|
T | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+5103T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739033 | ||||||
| chr6:154739098
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+5168G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739098 | ||||||
| chr6:154739294
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+5364A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739294 | ||||||
| chr6:154739317
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+5387T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739317 | ||||||
| chr6:154739402
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.30+5472C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739402 | ||||||
| chr6:154739454
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+5524T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739454 | ||||||
| chr6:154739515
|
T | C | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0122others(2): Show | 5 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+5585T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739515 | ||||||
| chr6:154739627
|
G | A | 2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5697G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739627 | ||||||
| chr6:154739654
|
C | T | 6 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0192others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+5724C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739654 | ||||||
| chr6:154739858
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+5928A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739858 | ||||||
| chr6:154740107
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+6177T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740107 | ||||||
| chr6:154740301
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.30+6371T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740301 | ||||||
| chr6:154740524
|
A | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+6594A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740524 | ||||||
| chr6:154740602
|
ATTTTCTT others(5): Show |
A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+6689_30+6700del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740602 | |||||
| chr6:154740625
|
C | CT | 97 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0085others(94): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.30+6709dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740625 | |||||
| chr6:154740625
|
C | CTT | 89 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.30+6708_30+6709dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740625 | |||||
| chr6:154740772
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+6842C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740772 | ||||||
| chr6:154740810
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+6880G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740810 | ||||||
| chr6:154741081
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.30+7151G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741081 | ||||||
| chr6:154741093
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+7163C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741093 | ||||||
| chr6:154741151
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.30+7221T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741151 | ||||||
| chr6:154741294
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30+7364G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741294 | ||||||
| chr6:154741596
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.30+7666G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741596 | ||||||
| chr6:154741649
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.30+7719C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741649 | ||||||
| chr6:154741653
|
C | T | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.30+7723C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741653 | ||||||
| chr6:154741669
|
A | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+7739A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741669 | ||||||
| chr6:154741670
|
G | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+7740G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741670 | ||||||
| chr6:154741697
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.30+7767G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741697 | ||||||
| chr6:154741702
|
C | T | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | HG02015.hp1 HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.30+7772C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741702 | ||||||
| chr6:154741730
|
G | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+7800G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741730 | ||||||
| chr6:154742076
|
G | A | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+8146G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742076 | ||||||
| chr6:154742156
|
T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+8226T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742156 | ||||||
| chr6:154742233
|
A | G | 6 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+8303A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742233 | ||||||
| chr6:154742506
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.30+8576A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742506 | ||||||
| chr6:154742649
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.30+8719T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742649 | ||||||
| chr6:154742742
|
CTTTA | C | 205 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.30+8819_30+8822del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154742742 | |||||
| chr6:154742833
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+8903A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742833 | ||||||
| chr6:154742914
|
C | T | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+8984C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742914 | ||||||
| chr6:154742925
|
T | C | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.30+8995T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742925 | ||||||
| chr6:154742953
|
A | AT | 157 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.30+9032dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154742953 | |||||
| chr6:154743541
|
G | A | 223 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.30+9611G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743541 | ||||||
| chr6:154743662
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+9732C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743662 | ||||||
| chr6:154743945
|
A | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+10015A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743945 | ||||||
| chr6:154743979
|
AATTTACC others(4): Show |
A | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+10055_30+10065d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154743979 | |||||
| chr6:154744145
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.30+10215T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744145 | ||||||
| chr6:154744215
|
C | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+10285C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744215 | ||||||
| chr6:154744485
|
C | T | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01496.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.30+10555C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744485 | ||||||
| chr6:154744768
|
C | A | 221 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.30+10838C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744768 | ||||||
| chr6:154744768
|
C | G | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.30+10838C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744768 | ||||||
| chr6:154744928
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+10998G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744928 | ||||||
| chr6:154744972
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.30+11042G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744972 | ||||||
| chr6:154745111
|
C | A | 1 | a0001c0001t0002g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.30+11181C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745111 | ||||||
| chr6:154745122
|
C | T | 1 | a0001c0014t0002g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.30+11192C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745122 | ||||||
| chr6:154745138
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+11208G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745138 | ||||||
| chr6:154745206
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.30+11276T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745206 | ||||||
| chr6:154745381
|
T | A | 56 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0091others(53): Show | 56 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+11451T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745381 | ||||||
| chr6:154745407
|
TC | T | 11 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(8): Show | 11 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+11478delC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745407 | ||||||
| chr6:154745545
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+11615T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745545 | ||||||
| chr6:154745570
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+11640G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745570 | ||||||
| chr6:154745811
|
T | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+11881T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745811 | ||||||
| chr6:154745894
|
T | C | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+11964T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745894 | ||||||
| chr6:154745976
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0189 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.30+12046C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745976 | ||||||
| chr6:154746126
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+12196T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746126 | ||||||
| chr6:154746176
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.30+12246G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746176 | ||||||
| chr6:154746192
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0179 | 2 | HG00621.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.30+12262A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746192 | ||||||
| chr6:154746392
|
A | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+12462A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746392 | ||||||
| chr6:154746431
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+12501T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746431 | ||||||
| chr6:154746491
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+12561A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746491 | ||||||
| chr6:154746536
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+12606C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746536 | ||||||
| chr6:154746654
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0252 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12724G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746654 | ||||||
| chr6:154746657
|
A | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0252 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12727A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746657 | ||||||
| chr6:154746659
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0252 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12729C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746659 | ||||||
| chr6:154746699
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+12769T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746699 | ||||||
| chr6:154747258
|
A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+13328A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747258 | ||||||
| chr6:154747410
|
G | C | 10 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0018others(7): Show | 10 | HG00597.hp1 HG00673.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+13480G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747410 | ||||||
| chr6:154747419
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+13489G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747419 | ||||||
| chr6:154747432
|
T | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+13502T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747432 | ||||||
| chr6:154747624
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.30+13694C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747624 | ||||||
| chr6:154747646
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+13716C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747646 | ||||||
| chr6:154747666
|
T | C | 9 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+13736T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747666 | ||||||
| chr6:154747702
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.30+13772T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747702 | ||||||
| chr6:154747764
|
T | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13834T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747764 | ||||||
| chr6:154747896
|
C | CTATG | 4 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0276others(1): Show | 4 | HG00621.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13967_30+13968i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTATGTG | 9 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+13967_30+13968i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTG | 43 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0098others(40): Show | 43 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+14006_30+14007d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTGTG | 17 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0103others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.30+14004_30+14007d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTGTGTG | 15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0104others(12): Show | 15 | HG00558.hp1 HG01070.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+14002_30+14007d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG00597.hp2 HG01256.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+14000_30+14007d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.30+13998_30+14007d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.30+13996_30+14007d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTG | C | 44 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0107others(41): Show | 44 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+14006_30+14007d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTG | C | 18 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0134others(15): Show | 18 | HG00544.hp2 HG00673.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+14004_30+14007d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTG | C | 57 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0089others(54): Show | 57 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+14002_30+14007d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0005g0152others(6): Show | 9 | HG02145.hp1 HG03017.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+14000_30+14007d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTGT others(3): Show |
C | 1 | a0002c0004t0001g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.30+13998_30+14007d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0165a0001c0001t0001g0172 | 2 | HG02717.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.30+13996_30+14007d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTGT others(7): Show |
C | 5 | a0001c0001t0003g0084a0001c0001t0003g0267a0001c0001t0003g0268others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+13994_30+14007d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747896
|
CTGTGTGT others(9): Show |
C | 5 | a0001c0001t0002g0026a0001c0001t0003g0080a0001c0001t0003g0081others(2): Show | 5 | HG02129.hp1 HG02258.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+13992_30+14007d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | |||||
| chr6:154747900
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.30+13970G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747900 | ||||||
| chr6:154748008
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.30+14078T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748008 | ||||||
| chr6:154748108
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.30+14178G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748108 | ||||||
| chr6:154748462
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+14532A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748462 | ||||||
| chr6:154748525
|
G | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+14595G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748525 | ||||||
| chr6:154748727
|
T | G | 1 | a0001c0001t0002g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.30+14797T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748727 | ||||||
| chr6:154748814
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0252 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+14884A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748814 | ||||||
| chr6:154749025
|
T | G | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0050others(1): Show | 4 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+15095T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749025 | ||||||
| chr6:154749092
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+15162G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749092 | ||||||
| chr6:154749123
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.30+15193G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749123 | ||||||
| chr6:154749175
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.30+15245C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749175 | ||||||
| chr6:154749188
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.30+15258G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749188 | ||||||
| chr6:154749231
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0252a0001c0011t0001g0208 | 3 | HG03098.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.30+15301G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749231 | ||||||
| chr6:154749247
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.30+15317C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749247 | ||||||
| chr6:154749494
|
T | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG00558.hp1 HG03942.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+15564T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749494 | ||||||
| chr6:154749614
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+15684G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749614 | ||||||
| chr6:154749654
|
A | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+15724A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749654 | ||||||
| chr6:154749673
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15743G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749673 | ||||||
| chr6:154749693
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.30+15763G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749693 | ||||||
| chr6:154749712
|
G | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15782G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749712 | ||||||
| chr6:154750018
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.30+16088G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750018 | ||||||
| chr6:154750251
|
T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+16321T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750251 | ||||||
| chr6:154750298
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+16368A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750298 | ||||||
| chr6:154750380
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+16450G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750380 | ||||||
| chr6:154750434
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+16504T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750434 | ||||||
| chr6:154750453
|
T | G | 17 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0172others(14): Show | 17 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+16523T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750453 | ||||||
| chr6:154750631
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.30+16701A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750631 | ||||||
| chr6:154750886
|
T | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+16956T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750886 | ||||||
| chr6:154750954
|
T | C | 1 | a0001c0001t0010g0088 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.30+17024T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750954 | ||||||
| chr6:154751033
|
T | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0264 | 2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.30+17103T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751033 | ||||||
| chr6:154751186
|
G | A | 86 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.30+17256G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751186 | ||||||
| chr6:154751269
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+17339C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751269 | ||||||
| chr6:154751301
|
T | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17371T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751301 | ||||||
| chr6:154751309
|
A | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17379A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751309 | ||||||
| chr6:154751854
|
T | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+17924T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751854 | ||||||
| chr6:154752029
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.30+18099C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752029 | ||||||
| chr6:154752072
|
T | G | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.30+18142T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752072 | ||||||
| chr6:154752098
|
T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+18168T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752098 | ||||||
| chr6:154752154
|
C | G | 5 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0045others(2): Show | 5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+18224C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752154 | ||||||
| chr6:154752422
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+18492C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752422 | ||||||
| chr6:154752423
|
T | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+18493T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752423 | ||||||
| chr6:154752523
|
C | T | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+18593C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752523 | ||||||
| chr6:154752729
|
T | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+18799T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752729 | ||||||
| chr6:154752978
|
G | C | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.30+19048G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752978 | ||||||
| chr6:154753012
|
G | GT | 7 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+19093dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154753012 | |||||
| chr6:154753016
|
T | TG | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+19086_30+19087i others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753016 | ||||||
| chr6:154753050
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.30+19120C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753050 | ||||||
| chr6:154753158
|
G | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+19228G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753158 | ||||||
| chr6:154753371
|
T | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+19441T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753371 | ||||||
| chr6:154753382
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+19452G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753382 | ||||||
| chr6:154753502
|
A | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+19572A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753502 | ||||||
| chr6:154753532
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+19602G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753532 | ||||||
| chr6:154753671
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+19741T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753671 | ||||||
| chr6:154753954
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+20024C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753954 | ||||||
| chr6:154753984
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0008t0002g0257 | 3 | HG01070.hp1 HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.31-20005C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753984 | ||||||
| chr6:154754042
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.31-19947G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754042 | ||||||
| chr6:154754087
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.31-19902A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754087 | ||||||
| chr6:154754321
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-19668C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754321 | ||||||
| chr6:154754377
|
G | A | 1 | a0001c0001t0009g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-19612G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754377 | ||||||
| chr6:154754472
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-19517A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754472 | ||||||
| chr6:154754524
|
G | A | 11 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-19465G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754524 | ||||||
| chr6:154754716
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31-19273T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754716 | ||||||
| chr6:154754794
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-19195T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754794 | ||||||
| chr6:154754797
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-19192T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754797 | ||||||
| chr6:154754835
|
T | A | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-19154T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754835 | ||||||
| chr6:154754859
|
C | G | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.31-19130C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754859 | ||||||
| chr6:154754886
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.31-19103A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754886 | ||||||
| chr6:154754958
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-19031T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754958 | ||||||
| chr6:154754959
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-19030C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754959 | ||||||
| chr6:154755013
|
G | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31-18976G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755013 | ||||||
| chr6:154755081
|
A | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-18908A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755081 | ||||||
| chr6:154755349
|
G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-18640G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755349 | ||||||
| chr6:154755367
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18622T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755367 | ||||||
| chr6:154755414
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-18575C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755414 | ||||||
| chr6:154755489
|
G | A | 185 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.31-18500G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755489 | ||||||
| chr6:154755502
|
C | T | 1 | a0002c0004t0001g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.31-18487C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755502 | ||||||
| chr6:154755503
|
G | A | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-18486G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755503 | ||||||
| chr6:154755503
|
G | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-18486G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755503 | ||||||
| chr6:154755529
|
A | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18460A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755529 | ||||||
| chr6:154755596
|
A | G | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-18393A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755596 | ||||||
| chr6:154755719
|
C | T | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18270C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755719 | ||||||
| chr6:154755892
|
C | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-18097C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755892 | ||||||
| chr6:154755894
|
C | G | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.31-18095C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755894 | ||||||
| chr6:154755941
|
G | A | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-18048G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755941 | ||||||
| chr6:154756017
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-17972A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756017 | ||||||
| chr6:154756075
|
A | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0263 | 2 | HG01515.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.31-17914A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756075 | ||||||
| chr6:154756238
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-17751C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756238 | ||||||
| chr6:154756727
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.31-17262A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756727 | ||||||
| chr6:154756737
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-17252G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756737 | ||||||
| chr6:154756749
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-17240G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756749 | ||||||
| chr6:154756831
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.31-17158C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756831 | ||||||
| chr6:154756835
|
C | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0113a0001c0001t0001g0116others(6): Show | 9 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-17154C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756835 | ||||||
| chr6:154756848
|
A | G | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-17141A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756848 | ||||||
| chr6:154756857
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.31-17132G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756857 | ||||||
| chr6:154756933
|
T | C | 5 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-17056T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756933 | ||||||
| chr6:154756939
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-17050G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756939 | ||||||
| chr6:154757088
|
C | T | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-16901C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757088 | ||||||
| chr6:154757315
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-16674C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757315 | ||||||
| chr6:154757360
|
G | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-16629G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757360 | ||||||
| chr6:154757507
|
C | T | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-16482C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757507 | ||||||
| chr6:154757863
|
C | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-16126C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757863 | ||||||
| chr6:154757914
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-16075T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757914 | ||||||
| chr6:154757950
|
A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-16039A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757950 | ||||||
| chr6:154758033
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-15956C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758033 | ||||||
| chr6:154758174
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-15815A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758174 | ||||||
| chr6:154758236
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-15753A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758236 | ||||||
| chr6:154758267
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-15722A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758267 | ||||||
| chr6:154758329
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31-15660C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758329 | ||||||
| chr6:154758335
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.31-15654C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758335 | ||||||
| chr6:154758451
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.31-15538A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758451 | ||||||
| chr6:154758462
|
T | C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-15527T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758462 | ||||||
| chr6:154758508
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.31-15481G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758508 | ||||||
| chr6:154758531
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-15458C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758531 | ||||||
| chr6:154758551
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-15438A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758551 | ||||||
| chr6:154758611
|
C | CT | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-15372dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154758611 | |||||
| chr6:154758978
|
A | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-15011A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758978 | ||||||
| chr6:154759104
|
T | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0278 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.31-14885T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759104 | ||||||
| chr6:154759125
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-14864C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759125 | ||||||
| chr6:154759483
|
G | A | 4 | a0004c0007t0001g0144a0004c0007t0001g0177a0005c0005t0002g0255others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-14506G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759483 | ||||||
| chr6:154759505
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.31-14484A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759505 | ||||||
| chr6:154759664
|
A | AT | 153 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(150): Show | 153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.31-14307dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154759664 | |||||
| chr6:154759664
|
AT | A | 32 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(29): Show | 32 | HG00621.hp2 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-14307delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154759664 | |||||
| chr6:154759767
|
G | A | 2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.31-14222G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759767 | ||||||
| chr6:154759831
|
A | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-14158A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759831 | ||||||
| chr6:154759849
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-14140A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759849 | ||||||
| chr6:154759987
|
G | A | 9 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-14002G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759987 | ||||||
| chr6:154760029
|
C | T | 205 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.31-13960C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760029 | ||||||
| chr6:154760087
|
T | TA | 9 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-13899dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154760087 | |||||
| chr6:154760512
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.31-13477G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760512 | ||||||
| chr6:154760563
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.31-13426A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760563 | ||||||
| chr6:154760713
|
GT | G | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-13268delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154760713 | |||||
| chr6:154760839
|
A | G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-13150A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760839 | ||||||
| chr6:154760974
|
T | A | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-13015T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760974 | ||||||
| chr6:154760985
|
A | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0230others(1): Show | 4 | NA18983.hp1 NA18998.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-13004A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760985 | ||||||
| chr6:154761067
|
G | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0147others(5): Show | 8 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-12922G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761067 | ||||||
| chr6:154761164
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31-12825C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761164 | ||||||
| chr6:154761311
|
C | A | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-12678C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761311 | ||||||
| chr6:154761523
|
T | C | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-12466T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761523 | ||||||
| chr6:154761540
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.31-12449C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761540 | ||||||
| chr6:154761668
|
A | C | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-12321A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761668 | ||||||
| chr6:154761845
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.31-12144C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761845 | ||||||
| chr6:154762090
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-11899A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762090 | ||||||
| chr6:154762123
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-11866C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762123 | ||||||
| chr6:154762183
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.31-11806A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762183 | ||||||
| chr6:154762213
|
T | G | 1 | a0001c0001t0003g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.31-11776T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762213 | ||||||
| chr6:154762585
|
A | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-11404A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762585 | ||||||
| chr6:154762687
|
A | G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11302A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762687 | ||||||
| chr6:154762755
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0264 | 2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.31-11234T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762755 | ||||||
| chr6:154762898
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-11091T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762898 | ||||||
| chr6:154762921
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.31-11068T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762921 | ||||||
| chr6:154763135
|
C | G | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-10854C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763135 | ||||||
| chr6:154763251
|
T | C | 169 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.31-10738T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763251 | ||||||
| chr6:154763274
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.31-10715T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763274 | ||||||
| chr6:154763289
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-10700T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763289 | ||||||
| chr6:154763310
|
T | C | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-10679T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763310 | ||||||
| chr6:154763311
|
C | T | 280 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.31-10678C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763311 | ||||||
| chr6:154763411
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.31-10578T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763411 | ||||||
| chr6:154763759
|
A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-10230A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763759 | ||||||
| chr6:154763793
|
C | G | 168 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.31-10196C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763793 | ||||||
| chr6:154763960
|
G | A | 223 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.31-10029G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763960 | ||||||
| chr6:154764067
|
T | C | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-9922T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764067 | ||||||
| chr6:154764100
|
A | G | 5 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9889A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764100 | ||||||
| chr6:154764142
|
T | C | 4 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9847T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764142 | ||||||
| chr6:154764277
|
C | CT | 200 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.31-9698dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154764277 | |||||
| chr6:154764340
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.31-9649A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764340 | ||||||
| chr6:154764385
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-9604A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764385 | ||||||
| chr6:154764519
|
A | C | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-9470A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764519 | ||||||
| chr6:154764761
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.31-9228A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764761 | ||||||
| chr6:154764797
|
T | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-9192T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764797 | ||||||
| chr6:154765019
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-8970G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765019 | ||||||
| chr6:154765099
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-8890A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765099 | ||||||
| chr6:154765104
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-8885C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765104 | ||||||
| chr6:154765186
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.31-8803C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765186 | ||||||
| chr6:154765459
|
T | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-8530T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765459 | ||||||
| chr6:154765504
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-8485C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765504 | ||||||
| chr6:154765540
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0236 | 2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.31-8449G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765540 | ||||||
| chr6:154765632
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.31-8357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765632 | ||||||
| chr6:154765700
|
A | ATTAT | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-8285_31-8282dup others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154765700 | |||||
| chr6:154765943
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.31-8046A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765943 | ||||||
| chr6:154766041
|
A | G | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-7948A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766041 | ||||||
| chr6:154766052
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0151a0001c0001t0001g0247 | 3 | HG00609.hp1 HG02155.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.31-7937A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766052 | ||||||
| chr6:154766061
|
TTAAAG | T | 47 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0001t0001g0094others(44): Show | 47 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.31-7924_31-7920del others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766061 | |||||
| chr6:154766068
|
A | G | 1 | a0001c0001t0004g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31-7921A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766068 | ||||||
| chr6:154766083
|
GTTA | G | 89 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.31-7902_31-7900del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766083 | |||||
| chr6:154766100
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-7889C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766100 | ||||||
| chr6:154766123
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-7866A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766123 | ||||||
| chr6:154766428
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-7561C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766428 | ||||||
| chr6:154766659
|
AC | A | 13 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-7320delC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766659 | |||||
| chr6:154766668
|
C | CT | 4 | a0001c0001t0001g0168a0001c0001t0001g0238a0001c0001t0001g0265others(1): Show | 4 | HG02486.hp2 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7321_31-7320ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | ||||||
| chr6:154766668
|
C | CTT | 5 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0155others(2): Show | 5 | HG02602.hp1 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7321_31-7320ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | ||||||
| chr6:154766668
|
C | T | 2 | a0001c0001t0001g0167a0001c0013t0002g0106 | 2 | HG03209.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.31-7321C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | ||||||
| chr6:154766669
|
C | CCT | 32 | a0001c0001t0001g0099a0001c0001t0001g0183a0001c0001t0001g0184others(29): Show | 32 | HG00621.hp2 HG01123.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-7320_31-7319ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766669 | ||||||
| chr6:154766669
|
C | CT | 51 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(48): Show | 51 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.31-7305dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | |||||
| chr6:154766669
|
C | CTT | 18 | a0001c0001t0001g0093a0001c0001t0001g0126a0001c0001t0001g0129others(15): Show | 18 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-7306_31-7305dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | |||||
| chr6:154766669
|
C | CTTT | 60 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(57): Show | 60 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.31-7307_31-7305dup others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | |||||
| chr6:154766669
|
C | T | 15 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0155others(12): Show | 15 | HG01109.hp1 HG02486.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-7320C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766669 | ||||||
| chr6:154766670
|
T | C | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.31-7319T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766670 | ||||||
| chr6:154766708
|
A | T | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-7281A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766708 | ||||||
| chr6:154766749
|
A | C | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-7240A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766749 | ||||||
| chr6:154766828
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-7161G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766828 | ||||||
| chr6:154766855
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-7134C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766855 | ||||||
| chr6:154766932
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-7057G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766932 | ||||||
| chr6:154767481
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-6508G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767481 | ||||||
| chr6:154767507
|
C | T | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-6482C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767507 | ||||||
| chr6:154767529
|
CT | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(47): Show | 50 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.31-6433delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | |||||
| chr6:154767529
|
CTT | C | 11 | a0001c0001t0002g0011a0001c0001t0002g0032a0001c0001t0002g0072others(8): Show | 11 | HG00621.hp2 HG01106.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-6434_31-6433del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | |||||
| chr6:154767529
|
CTTT | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0172others(29): Show | 32 | HG01123.hp1 HG01167.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-6435_31-6433del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | |||||
| chr6:154767529
|
CTTTTTTT others(3): Show |
C | 166 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.31-6442_31-6433del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | |||||
| chr6:154767657
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-6332A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767657 | ||||||
| chr6:154767911
|
A | T | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.31-6078A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767911 | ||||||
| chr6:154767971
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-6018C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767971 | ||||||
| chr6:154768015
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-5974T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768015 | ||||||
| chr6:154768336
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-5653T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768336 | ||||||
| chr6:154768483
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | NA18993.hp2 NA19088.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.31-5506A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768483 | ||||||
| chr6:154768492
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-5497G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768492 | ||||||
| chr6:154768578
|
C | G | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.31-5411C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768578 | ||||||
| chr6:154769036
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.31-4953G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769036 | ||||||
| chr6:154769044
|
C | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-4945C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769044 | ||||||
| chr6:154769060
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-4929C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769060 | ||||||
| chr6:154769062
|
CA | C | 57 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-4903delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | |||||
| chr6:154769062
|
CAA | C | 14 | a0001c0001t0001g0110a0001c0001t0001g0171a0001c0001t0001g0183others(11): Show | 14 | HG00642.hp2 HG01169.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-4904_31-4903del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | |||||
| chr6:154769062
|
CAAA | C | 106 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0085others(103): Show | 106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.31-4905_31-4903del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | |||||
| chr6:154769062
|
CAAAA | C | 84 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(81): Show | 84 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.31-4906_31-4903del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | |||||
| chr6:154769063
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.31-4926A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769063 | ||||||
| chr6:154769201
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-4788G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769201 | ||||||
| chr6:154769628
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4361G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769628 | ||||||
| chr6:154770074
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-3915G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770074 | ||||||
| chr6:154770101
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-3888G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770101 | ||||||
| chr6:154770210
|
G | T | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-3779G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770210 | ||||||
| chr6:154770276
|
A | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3713A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770276 | ||||||
| chr6:154770334
|
T | C | 194 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.31-3655T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770334 | ||||||
| chr6:154770339
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0248 | 2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.31-3650C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770339 | ||||||
| chr6:154770386
|
ACACTCTC others(7): Show |
A | 3 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0132 | 3 | HG01074.hp2 HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-3601_31-3588del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770386 | |||||
| chr6:154770388
|
A | ACACACTC others(23): Show |
1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31-3600_31-3599ins others(30): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
A | ACACACTC others(51): Show |
1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-3600_31-3599ins others(58): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
A | ACT | 8 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0018others(5): Show | 8 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-3566_31-3565dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
A | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(5): Show | 8 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3601A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770388 | ||||||
| chr6:154770388
|
ACTCT | A | 8 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0015others(5): Show | 8 | HG00642.hp2 HG01123.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3568_31-3565del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCT | A | 7 | a0001c0001t0002g0200a0001c0001t0003g0080a0001c0001t0003g0081others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-3570_31-3565del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCTC others(3): Show |
A | 14 | a0001c0001t0002g0073a0001c0001t0002g0075a0001c0001t0002g0076others(11): Show | 14 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-3574_31-3565del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCTC others(5): Show |
A | 6 | a0001c0001t0001g0129a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG00558.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-3576_31-3565del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCTC others(7): Show |
A | 173 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.31-3578_31-3565del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCTC others(11): Show |
A | 2 | a0001c0001t0001g0214a0001c0001t0001g0238 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.31-3582_31-3565del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770388
|
ACTCTCTC others(13): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.31-3584_31-3565del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | |||||
| chr6:154770390
|
T | A | 4 | a0001c0008t0002g0257a0003c0003t0002g0272a0003c0003t0002g0273others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3599T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770390 | ||||||
| chr6:154770392
|
T | A | 2 | a0003c0003t0002g0272a0003c0003t0002g0273 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-3597T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770392 | ||||||
| chr6:154770396
|
T | A | 2 | a0001c0001t0002g0200a0001c0013t0002g0106 | 2 | HG02717.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.31-3593T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770396 | ||||||
| chr6:154770398
|
T | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-3591T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770398 | ||||||
| chr6:154770400
|
T | A | 8 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-3589T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770400 | ||||||
| chr6:154770402
|
T | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0265a0001c0001t0001g0271others(1): Show | 4 | HG00558.hp2 HG02723.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3587T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770402 | ||||||
| chr6:154770404
|
T | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG00609.hp2 HG02040.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.31-3585T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770404 | ||||||
| chr6:154770425
|
A | C | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-3564A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770425 | ||||||
| chr6:154770457
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.31-3532G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770457 | ||||||
| chr6:154770537
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-3452C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770537 | ||||||
| chr6:154770540
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.31-3449C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770540 | ||||||
| chr6:154770816
|
C | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-3173C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770816 | ||||||
| chr6:154770954
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-3035A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770954 | ||||||
| chr6:154771047
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-2942G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771047 | ||||||
| chr6:154771065
|
T | C | 156 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.31-2924T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771065 | ||||||
| chr6:154771126
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-2863G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771126 | ||||||
| chr6:154771268
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-2721C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771268 | ||||||
| chr6:154771323
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.31-2666A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771323 | ||||||
| chr6:154771467
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-2522A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771467 | ||||||
| chr6:154771651
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-2338C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771651 | ||||||
| chr6:154772021
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-1968C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772021 | ||||||
| chr6:154772158
|
GTTAA | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-1826_31-1823del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154772158 | |||||
| chr6:154772231
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.31-1758C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772231 | ||||||
| chr6:154772324
|
G | T | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.31-1665G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772324 | ||||||
| chr6:154772432
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-1557G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772432 | ||||||
| chr6:154772470
|
G | A | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-1519G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772470 | ||||||
| chr6:154772489
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-1500A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772489 | ||||||
| chr6:154772637
|
C | T | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.31-1352C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772637 | ||||||
| chr6:154772702
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.31-1287A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772702 | ||||||
| chr6:154772713
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.31-1276A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772713 | ||||||
| chr6:154772919
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-1070T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772919 | ||||||
| chr6:154773148
|
C | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-841C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773148 | ||||||
| chr6:154773231
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.31-758C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773231 | ||||||
| chr6:154773416
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-573G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773416 | ||||||
| chr6:154773630
|
A | G | 205 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.31-359A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773630 | ||||||
| chr6:154773717
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-272C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773717 | ||||||
| chr6:154773854
|
G | A | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-135G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773854 | ||||||
| chr6:154773868
|
G | T | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-121G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773868 | ||||||
| chr6:154774118
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+46A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774118 | ||||||
| chr6:154774233
|
C | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+161C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774233 | ||||||
| chr6:154774272
|
C | G | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+200C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774272 | ||||||
| chr6:154774357
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.114+285G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774357 | ||||||
| chr6:154774430
|
C | A | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114+358C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774430 | ||||||
| chr6:154774997
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0150 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.114+925A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774997 | ||||||
| chr6:154775137
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.114+1065A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775137 | ||||||
| chr6:154775253
|
C | T | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.114+1181C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775253 | ||||||
| chr6:154775273
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.114+1201T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775273 | ||||||
| chr6:154775328
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.114+1256T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775328 | ||||||
| chr6:154775534
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1462G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775534 | ||||||
| chr6:154775640
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.114+1568C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775640 | ||||||
| chr6:154775652
|
C | G | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1580C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775652 | ||||||
| chr6:154775653
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.114+1581C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775653 | ||||||
| chr6:154775959
|
G | A | 209 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.114+1887G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775959 | ||||||
| chr6:154775959
|
G | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0189a0002c0004t0001g0186others(2): Show | 5 | HG02145.hp1 HG02735.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1887G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775959 | ||||||
| chr6:154776287
|
GTGTATAT others(7): Show |
G | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.115-1712_115-1699d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776287 | |||||
| chr6:154776289
|
GTATATAT others(7): Show |
G | 185 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.115-1693_115-1680d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776289 | |||||
| chr6:154776297
|
GTA | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(2): Show | 5 | HG02451.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-1692_115-1691d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776297 | |||||
| chr6:154776396
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-1605A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154776396 | ||||||
| chr6:154776536
|
A | G | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-1465A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154776536 | ||||||
| chr6:154777019
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.115-982A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777019 | ||||||
| chr6:154777168
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-833G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777168 | ||||||
| chr6:154777172
|
G | C | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.115-829G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777172 | ||||||
| chr6:154777183
|
A | AG | 7 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-814dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154777183 | |||||
| chr6:154777188
|
A | G | 9 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-813A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777188 | ||||||
| chr6:154777253
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.115-748T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777253 | ||||||
| chr6:154777429
|
C | T | 1 | a0001c0006t0001g0254 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.115-572C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777429 | ||||||
| chr6:154777468
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.115-533T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777468 | ||||||
| chr6:154777589
|
A | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-412A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777589 | ||||||
| chr6:154777756
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.115-245A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777756 | ||||||
| chr6:154777834
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-167C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777834 | ||||||
| chr6:154777849
|
A | G | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-152A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777849 | ||||||
| chr6:154778237
|
C | T | 205 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.159+192C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778237 | ||||||
| chr6:154778280
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+235C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778280 | ||||||
| chr6:154778348
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0278 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+303C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778348 | ||||||
| chr6:154778378
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+333A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778378 | ||||||
| chr6:154778380
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.159+335T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778380 | ||||||
| chr6:154778546
|
C | G | 86 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.159+501C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778546 | ||||||
| chr6:154778768
|
A | AGT | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0076others(6): Show | 9 | HG00621.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | ||||||
| chr6:154778768
|
A | AGTGT | 4 | a0001c0001t0002g0075a0001c0001t0002g0077a0001c0001t0002g0276others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | ||||||
| chr6:154778768
|
A | AGTGTGT | 5 | a0001c0001t0002g0074a0001c0001t0002g0078a0001c0001t0002g0079others(2): Show | 5 | HG01123.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | ||||||
| chr6:154778769
|
A | ATG | 78 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0093others(75): Show | 78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.159+764_159+765dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
A | ATGTG | 24 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0132others(21): Show | 24 | HG00642.hp2 HG01074.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.159+762_159+765dup others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
A | ATGTGTG | 6 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0149others(3): Show | 6 | HG00140.hp1 HG00741.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+760_159+765dup others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0251a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+758_159+765dup others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
A | G | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+724A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778769 | ||||||
| chr6:154778769
|
ATG | A | 8 | a0001c0001t0001g0118a0001c0001t0001g0170a0001c0001t0001g0175others(5): Show | 8 | HG01070.hp2 HG01981.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+764_159+765del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
ATGTG | A | 20 | a0001c0001t0001g0064a0001c0001t0001g0105a0001c0001t0001g0117others(17): Show | 20 | HG02148.hp1 HG02258.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.159+762_159+765del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
ATGTGTG | A | 6 | a0001c0001t0001g0171a0001c0001t0003g0267a0001c0001t0003g0268others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+760_159+765del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0172a0001c0001t0002g0021 | 2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.159+756_159+765del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778769
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.159+752_159+765del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | |||||
| chr6:154778836
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.159+791T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778836 | ||||||
| chr6:154778937
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.159+892G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778937 | ||||||
| chr6:154778943
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+898C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778943 | ||||||
| chr6:154779024
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+979T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779024 | ||||||
| chr6:154779071
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+1026C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779071 | ||||||
| chr6:154779088
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+1043A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779088 | ||||||
| chr6:154779276
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+1231T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779276 | ||||||
| chr6:154779359
|
T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+1314T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779359 | ||||||
| chr6:154779414
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.159+1369G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779414 | ||||||
| chr6:154779673
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1628G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779673 | ||||||
| chr6:154779758
|
G | GGT | 5 | a0001c0001t0002g0003a0001c0001t0002g0036a0001c0001t0002g0047others(2): Show | 5 | HG02273.hp2 HG02280.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1736_159+1737d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779758 | |||||
| chr6:154779759
|
G | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1714G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779759 | ||||||
| chr6:154779777
|
GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.159+1734_159+1745d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779777 | |||||
| chr6:154779779
|
GTGTATAT others(3): Show |
G | 12 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0172others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1736_159+1745d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779779 | |||||
| chr6:154779779
|
GTGTATAT others(5): Show |
G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159+1736_159+1747d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779779 | |||||
| chr6:154779781
|
G | GTGTA | 5 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0045others(2): Show | 5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1737_159+1738i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
G | GTGTATAT others(1): Show |
3 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269 | 3 | HG01109.hp1 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.159+1737_159+1738i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0003g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159+1737_159+1738i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
GTA | G | 58 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0090others(55): Show | 58 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.159+1755_159+1756d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
GTATA | G | 19 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0105others(16): Show | 19 | HG00140.hp1 HG00733.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+1753_159+1756d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
GTATATA | G | 81 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(78): Show | 81 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.159+1751_159+1756d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
GTATATAT others(1): Show |
G | 21 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(18): Show | 21 | HG00621.hp2 HG01167.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.159+1749_159+1756d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779781
|
GTATATAT others(3): Show |
G | 4 | a0003c0003t0002g0273a0003c0003t0002g0274a0005c0005t0002g0255others(1): Show | 4 | HG02886.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1747_159+1756d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | |||||
| chr6:154779783
|
A | G | 63 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(60): Show | 63 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.159+1738A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779783 | ||||||
| chr6:154779785
|
A | G | 67 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(64): Show | 67 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.159+1740A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779785 | ||||||
| chr6:154779787
|
A | G | 12 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0105others(9): Show | 12 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1742A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779787 | ||||||
| chr6:154779789
|
A | G | 93 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.159+1744A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779789 | ||||||
| chr6:154779791
|
A | G | 17 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(14): Show | 17 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.159+1746A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779791 | ||||||
| chr6:154779793
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+1748A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779793 | ||||||
| chr6:154779813
|
T | A | 15 | a0001c0001t0002g0039a0001c0001t0002g0075a0001c0001t0002g0076others(12): Show | 15 | HG01358.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+1768T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779813 | ||||||
| chr6:154780019
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0239a0001c0001t0001g0241others(1): Show | 4 | HG02015.hp2 HG02155.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1974G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780019 | ||||||
| chr6:154780354
|
C | CT | 40 | a0001c0001t0001g0116a0001c0001t0001g0179a0001c0001t0002g0047others(37): Show | 40 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.159+2327dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780354 | |||||
| chr6:154780354
|
CT | C | 19 | a0001c0001t0001g0092a0001c0001t0001g0107a0001c0001t0001g0108others(16): Show | 19 | HG00140.hp2 HG01070.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+2327delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780354 | |||||
| chr6:154780405
|
CAT | C | 59 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0091others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.159+2362_159+2363d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780405 | |||||
| chr6:154780453
|
C | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2408C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780453 | ||||||
| chr6:154780534
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.159+2489C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780534 | ||||||
| chr6:154780583
|
T | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+2538T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780583 | ||||||
| chr6:154780772
|
T | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0050others(1): Show | 4 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2727T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780772 | ||||||
| chr6:154780809
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+2764C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780809 | ||||||
| chr6:154780819
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.159+2774G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780819 | ||||||
| chr6:154780957
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+2912C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780957 | ||||||
| chr6:154781103
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.159+3058A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781103 | ||||||
| chr6:154781117
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.159+3072T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781117 | ||||||
| chr6:154781156
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0232 | 2 | HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.159+3111A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781156 | ||||||
| chr6:154781498
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+3453C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781498 | ||||||
| chr6:154781551
|
A | G | 19 | a0001c0001t0001g0065a0001c0001t0001g0092a0001c0001t0001g0093others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+3506A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781551 | ||||||
| chr6:154781668
|
T | C | 170 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.159+3623T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781668 | ||||||
| chr6:154781673
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.159+3628A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781673 | ||||||
| chr6:154781687
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159+3642C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781687 | ||||||
| chr6:154781977
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.159+3932A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781977 | ||||||
| chr6:154782116
|
A | G | 78 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(75): Show | 78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.159+4071A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782116 | ||||||
| chr6:154782222
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.159+4177C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782222 | ||||||
| chr6:154782286
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+4241G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782286 | ||||||
| chr6:154782404
|
G | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0113a0001c0001t0001g0116others(6): Show | 9 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+4359G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782404 | ||||||
| chr6:154782417
|
T | TCAAAACA others(3): Show |
2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+4382_159+4391d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154782417 | |||||
| chr6:154782417
|
T | TCAAAACA others(8): Show |
1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+4377_159+4391d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154782417 | |||||
| chr6:154782549
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.159+4504T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782549 | ||||||
| chr6:154782572
|
A | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+4527A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782572 | ||||||
| chr6:154782747
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+4702C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782747 | ||||||
| chr6:154782761
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+4716G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782761 | ||||||
| chr6:154783117
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.160-4744A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783117 | ||||||
| chr6:154783140
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160-4721T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783140 | ||||||
| chr6:154783231
|
T | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-4630T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783231 | ||||||
| chr6:154783249
|
T | A | 16 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0172others(13): Show | 16 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-4612T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783249 | ||||||
| chr6:154783298
|
C | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-4563C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783298 | ||||||
| chr6:154783310
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.160-4551T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783310 | ||||||
| chr6:154783357
|
A | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-4504A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783357 | ||||||
| chr6:154783694
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-4167A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783694 | ||||||
| chr6:154783700
|
A | G | 17 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0171others(14): Show | 17 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.160-4161A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783700 | ||||||
| chr6:154783897
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-3964C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783897 | ||||||
| chr6:154783908
|
A | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3953A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783908 | ||||||
| chr6:154783974
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160-3887G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783974 | ||||||
| chr6:154784050
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3811G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784050 | ||||||
| chr6:154784105
|
T | C | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.160-3756T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784105 | ||||||
| chr6:154784120
|
G | GAGAGAGA others(3): Show |
1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160-3740_160-3739i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GAT | 10 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0105others(7): Show | 10 | HG00140.hp2 HG01109.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-3704_160-3703d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATAT | 4 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0002g0058others(1): Show | 4 | HG01516.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-3706_160-3703d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATAT | 7 | a0001c0001t0001g0175a0001c0001t0001g0191a0001c0001t0002g0031others(4): Show | 7 | HG00735.hp2 HG01070.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-3708_160-3703d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(1): Show |
5 | a0001c0001t0001g0111a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3710_160-3703d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(3): Show |
2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.160-3712_160-3703d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(5): Show |
1 | a0001c0001t0002g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160-3714_160-3703d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(7): Show |
1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-3716_160-3703d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(9): Show |
5 | a0001c0001t0001g0097a0001c0001t0001g0157a0001c0001t0001g0172others(2): Show | 5 | HG02080.hp1 HG02717.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3718_160-3703d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(11): Show |
2 | a0001c0001t0001g0137a0001c0001t0007g0112 | 2 | HG02886.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.160-3720_160-3703d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.160-3722_160-3703d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(15): Show |
1 | a0001c0001t0001g0096 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160-3724_160-3703d others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(17): Show |
1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-3726_160-3703d others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
G | GATATATA others(23): Show |
1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.160-3732_160-3703d others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GAT | G | 16 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0002g0002others(13): Show | 16 | HG00733.hp2 HG01070.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-3704_160-3703d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATAT | G | 21 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0010others(18): Show | 21 | HG00597.hp1 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-3706_160-3703d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATAT | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0271others(2): Show | 5 | HG02080.hp2 HG03486.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3708_160-3703d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(1): Show |
G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3710_160-3703d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(3): Show |
G | 5 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3712_160-3703d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(5): Show |
G | 8 | a0001c0001t0001g0147a0001c0001t0002g0075a0001c0001t0002g0076others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-3714_160-3703d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(7): Show |
G | 6 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3716_160-3703d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(9): Show |
G | 2 | a0001c0001t0002g0072a0001c0001t0002g0074 | 2 | HG00621.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.160-3718_160-3703d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(15): Show |
G | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-3724_160-3703d others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(17): Show |
G | 79 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(76): Show | 79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.160-3726_160-3703d others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784120
|
GATATATA others(23): Show |
G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3732_160-3703d others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | |||||
| chr6:154784122
|
T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3739T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784122 | ||||||
| chr6:154784124
|
T | G | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0263others(1): Show | 4 | HG01167.hp1 HG01433.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3737T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784124 | ||||||
| chr6:154784126
|
T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3735T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784126 | ||||||
| chr6:154784128
|
T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3733T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784128 | ||||||
| chr6:154784138
|
T | TATATAG | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0101others(3): Show | 6 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-3718_160-3717i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784138 | |||||
| chr6:154784147
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160-3710_160-3699d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784147 | |||||
| chr6:154784149
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160-3708_160-3699d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784149 | |||||
| chr6:154784155
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0107 | 2 | HG00733.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.160-3703_160-3702i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0141others(1): Show | 4 | HG01952.hp2 HG02602.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(7): Show |
6 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0229others(3): Show | 6 | HG00735.hp1 HG02071.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(3): Show |
6 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0138others(3): Show | 6 | HG00408.hp1 HG02004.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(1): Show |
8 | a0001c0001t0001g0091a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00558.hp1 HG01891.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0244 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATT | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0102others(3): Show | 6 | HG02257.hp1 HG03490.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATATTT others(3): Show |
5 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0133others(2): Show | 5 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATT | 5 | a0001c0001t0001g0070a0001c0001t0001g0145a0001c0001t0001g0163others(2): Show | 5 | HG02723.hp1 NA18942.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3692_160-3689d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATATTTAT others(1): Show |
3 | a0001c0001t0001g0135a0001c0001t0001g0167a0001c0001t0001g0247 | 3 | HG01261.hp1 HG02155.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.160-3696_160-3689d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATTTATT | 3 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0155 | 3 | HG01515.hp1 HG01517.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.160-3705_160-3704i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.160-3705_160-3704i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | |||||
| chr6:154784155
|
A | T | 28 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0101others(25): Show | 28 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.160-3706A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784155 | ||||||
| chr6:154784159
|
T | A | 2 | a0001c0001t0001g0172a0005c0005t0002g0255 | 2 | HG02717.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-3702T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784159 | ||||||
| chr6:154784393
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160-3468T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784393 | ||||||
| chr6:154784453
|
C | A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.160-3408C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784453 | ||||||
| chr6:154784784
|
C | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3077C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784784 | ||||||
| chr6:154784851
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3010T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784851 | ||||||
| chr6:154784863
|
C | T | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.160-2998C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784863 | ||||||
| chr6:154784918
|
A | G | 156 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.160-2943A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784918 | ||||||
| chr6:154784960
|
C | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-2901C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784960 | ||||||
| chr6:154785015
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160-2846G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785015 | ||||||
| chr6:154785017
|
C | A | 185 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.160-2844C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785017 | ||||||
| chr6:154785101
|
A | G | 8 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0116others(5): Show | 8 | HG00621.hp1 HG00741.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-2760A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785101 | ||||||
| chr6:154785143
|
T | C | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.160-2718T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785143 | ||||||
| chr6:154785154
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.160-2707T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785154 | ||||||
| chr6:154785249
|
T | C | 1 | a0001c0006t0001g0254 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-2612T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785249 | ||||||
| chr6:154785414
|
A | C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-2447A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785414 | ||||||
| chr6:154785445
|
C | G | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2416C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785445 | ||||||
| chr6:154785588
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG03579.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.160-2273C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785588 | ||||||
| chr6:154785684
|
A | ATTAT | 223 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.160-2174_160-2173i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154785684 | |||||
| chr6:154785824
|
G | T | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-2037G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785824 | ||||||
| chr6:154785838
|
C | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2023C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785838 | ||||||
| chr6:154785906
|
A | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-1955A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785906 | ||||||
| chr6:154785948
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-1913G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785948 | ||||||
| chr6:154786029
|
C | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-1832C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786029 | ||||||
| chr6:154786423
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.160-1438C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786423 | ||||||
| chr6:154786602
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0014t0002g0052 | 3 | HG01070.hp2 HG01433.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.160-1259G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786602 | ||||||
| chr6:154786624
|
G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160-1237G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786624 | ||||||
| chr6:154786772
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.160-1089G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786772 | ||||||
| chr6:154786886
|
A | AAAGAACT others(30): Show |
1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.160-972_160-936dup others(37): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154786886 | |||||
| chr6:154787005
|
A | T | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-856A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787005 | ||||||
| chr6:154787044
|
A | G | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160-817A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787044 | ||||||
| chr6:154787071
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160-790G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787071 | ||||||
| chr6:154787091
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-770G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787091 | ||||||
| chr6:154787253
|
G | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0136 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.160-608G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787253 | ||||||
| chr6:154787547
|
T | G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-314T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787547 | ||||||
| chr6:154787640
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160-221A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787640 | ||||||
| chr6:154788175
|
G | A | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.321+153G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788175 | ||||||
| chr6:154788226
|
CTGTGTTA others(30): Show |
C | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.321+207_321+243del others(37): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154788226 | |||||
| chr6:154788272
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+250A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788272 | ||||||
| chr6:154788290
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+268C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788290 | ||||||
| chr6:154788545
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0238 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.321+523T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788545 | ||||||
| chr6:154788698
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.321+676C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788698 | ||||||
| chr6:154788700
|
A | G | 5 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0045others(2): Show | 5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+678A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788700 | ||||||
| chr6:154788729
|
C | G | 1 | a0001c0001t0002g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.321+707C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788729 | ||||||
| chr6:154788792
|
T | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01106.hp1 HG01261.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+770T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788792 | ||||||
| chr6:154788913
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+891G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788913 | ||||||
| chr6:154788970
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0164 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.321+948G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788970 | ||||||
| chr6:154789216
|
C | G | 85 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.321+1194C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789216 | ||||||
| chr6:154789224
|
T | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+1202T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789224 | ||||||
| chr6:154789300
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+1278A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789300 | ||||||
| chr6:154789343
|
C | T | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.321+1321C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789343 | ||||||
| chr6:154789544
|
A | AT | 16 | a0001c0001t0001g0094a0001c0001t0001g0125a0001c0001t0001g0126others(13): Show | 16 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+1541dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154789544 | |||||
| chr6:154789770
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.321+1748C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789770 | ||||||
| chr6:154789787
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1765C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789787 | ||||||
| chr6:154789837
|
G | T | 1 | a0002c0004t0001g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.321+1815G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789837 | ||||||
| chr6:154789872
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1850A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789872 | ||||||
| chr6:154789931
|
A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1909A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789931 | ||||||
| chr6:154790225
|
G | T | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.321+2203G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790225 | ||||||
| chr6:154790291
|
G | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.321+2269G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790291 | ||||||
| chr6:154790432
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322-2391C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790432 | ||||||
| chr6:154790489
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.322-2305_322-2295d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.322-2306_322-2295d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.322-2307_322-2295d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.322-2309_322-2295d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0002g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-2311_322-2295d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0002g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.322-2313_322-2295d others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
AT | A | 15 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-2295delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATT | A | 12 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0038others(9): Show | 12 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.322-2296_322-2295d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0001g0090a0001c0001t0001g0140a0001c0001t0004g0197others(3): Show | 6 | HG00735.hp1 HG01255.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-2303_322-2295d others(11): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(3): Show |
A | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0089others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-2304_322-2295d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(4): Show |
A | 68 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.322-2305_322-2295d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(5): Show |
A | 57 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0001g0087others(54): Show | 57 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.322-2306_322-2295d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(6): Show |
A | 11 | a0001c0001t0001g0091a0001c0001t0001g0116a0001c0001t0001g0119others(8): Show | 11 | HG01515.hp1 HG01516.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-2307_322-2295d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(7): Show |
A | 6 | a0001c0001t0001g0192a0001c0001t0002g0074a0001c0001t0002g0276others(3): Show | 6 | HG01123.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2308_322-2295d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(8): Show |
A | 22 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(19): Show | 22 | HG00621.hp2 HG01496.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.322-2309_322-2295d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(9): Show |
A | 6 | a0001c0001t0001g0172a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2310_322-2295d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(10): Show |
A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2311_322-2295d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0002g0063 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.322-2313_322-2295d others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0002g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.322-2314_322-2295d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790489
|
ATTTTTTT others(14): Show |
A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.322-2315_322-2295d others(23): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | |||||
| chr6:154790505
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.322-2318T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790505 | ||||||
| chr6:154790589
|
C | T | 223 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.322-2234C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790589 | ||||||
| chr6:154790619
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.322-2204T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790619 | ||||||
| chr6:154790687
|
T | A | 1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.322-2136T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790687 | ||||||
| chr6:154790790
|
G | A | 210 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.322-2033G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790790 | ||||||
| chr6:154790911
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.322-1912A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790911 | ||||||
| chr6:154790934
|
A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.322-1889A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790934 | ||||||
| chr6:154791160
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0241 | 2 | HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.322-1663A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791160 | ||||||
| chr6:154791166
|
T | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-1657T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791166 | ||||||
| chr6:154791238
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.322-1585C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791238 | ||||||
| chr6:154791421
|
T | A | 1 | a0001c0001t0002g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-1402T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791421 | ||||||
| chr6:154791570
|
C | G | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.322-1253C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791570 | ||||||
| chr6:154791640
|
G | GT | 73 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0090others(70): Show | 73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.322-1176dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154791640 | |||||
| chr6:154791647
|
T | TA | 89 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.322-1170dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154791647 | |||||
| chr6:154791706
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.322-1117C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791706 | ||||||
| chr6:154791730
|
G | A | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-1093G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791730 | ||||||
| chr6:154791789
|
A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.322-1034A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791789 | ||||||
| chr6:154791974
|
T | C | 179 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.322-849T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791974 | ||||||
| chr6:154791992
|
A | G | 163 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.322-831A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791992 | ||||||
| chr6:154792098
|
C | T | 89 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.322-725C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792098 | ||||||
| chr6:154792239
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-584A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792239 | ||||||
| chr6:154792466
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.322-357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792466 | ||||||
| chr6:154792574
|
T | C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.322-249T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792574 | ||||||
| chr6:154792738
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.322-85C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792738 | ||||||
| chr6:154792994
|
A | G | 2 | a0001c0006t0001g0223a0001c0006t0001g0254 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.475+18A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154792994 | ||||||
| chr6:154793063
|
G | A | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+87G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793063 | ||||||
| chr6:154793080
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0211 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.475+104G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793080 | ||||||
| chr6:154793252
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.475+276G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793252 | ||||||
| chr6:154793343
|
T | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.475+367T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793343 | ||||||
| chr6:154793380
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.475+404T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793380 | ||||||
| chr6:154793412
|
T | A | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.475+436T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793412 | ||||||
| chr6:154793454
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+478A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793454 | ||||||
| chr6:154793455
|
A | T | 168 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.475+479A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793455 | ||||||
| chr6:154793466
|
A | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+490A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793466 | ||||||
| chr6:154793471
|
T | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+495T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793471 | ||||||
| chr6:154793510
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.475+534G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793510 | ||||||
| chr6:154793565
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.475+589A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793565 | ||||||
| chr6:154793575
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.475+599G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793575 | ||||||
| chr6:154793622
|
C | G | 1 | a0001c0001t0008g0156 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.475+646C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793622 | ||||||
| chr6:154793674
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0236 | 2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.475+698G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793674 | ||||||
| chr6:154793734
|
G | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0172others(13): Show | 16 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.475+758G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793734 | ||||||
| chr6:154793771
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.475+795C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793771 | ||||||
| chr6:154793815
|
C | CA | 146 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.475+863dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | |||||
| chr6:154793815
|
C | CAA | 33 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0105others(30): Show | 33 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.475+862_475+863dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | |||||
| chr6:154793815
|
CA | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0029others(6): Show | 9 | HG00621.hp2 HG02129.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+863delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | |||||
| chr6:154793839
|
A | AT | 10 | a0001c0001t0001g0086a0001c0001t0001g0181a0001c0001t0001g0182others(7): Show | 10 | HG01884.hp1 HG02300.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+870dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793839 | |||||
| chr6:154793839
|
A | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+863A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793839 | ||||||
| chr6:154793840
|
T | A | 2 | a0001c0001t0001g0233a0001c0001t0002g0006 | 2 | HG02135.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.475+864T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793840 | ||||||
| chr6:154793905
|
G | GTGTGTGT others(5): Show |
214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.475+932_475+943dup others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793905 | |||||
| chr6:154794017
|
C | G | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.476-992C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794017 | ||||||
| chr6:154794220
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.476-789G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794220 | ||||||
| chr6:154794628
|
A | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.476-381A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794628 | ||||||
| chr6:154794759
|
T | TG | 36 | a0001c0001t0001g0099a0001c0001t0001g0172a0001c0001t0001g0204others(33): Show | 36 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.476-237dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794759 | |||||
| chr6:154794759
|
TG | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0182a0001c0001t0001g0192others(13): Show | 16 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.476-237delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794759 | |||||
| chr6:154794769
|
G | C | 81 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.476-240G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794769 | ||||||
| chr6:154794769
|
G | GC | 4 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0133others(1): Show | 4 | HG01192.hp1 HG01361.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-240_476-239ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794769 | ||||||
| chr6:154794771
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.476-238G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794771 | ||||||
| chr6:154794772
|
GT | G | 29 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(26): Show | 29 | HG00099.hp1 HG00544.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-236delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794772
|
GTGTGGGG others(3): Show |
G | 3 | a0001c0001t0001g0129a0001c0001t0002g0075a0001c0001t0005g0196 | 3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-236_476-227del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794772
|
GTGTGGGG others(5): Show |
G | 1 | a0001c0001t0002g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.476-236_476-225del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794772
|
GTGTGGGG others(7): Show |
G | 3 | a0001c0001t0001g0212a0001c0001t0002g0074a0001c0001t0002g0076 | 3 | HG01123.hp1 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.476-236_476-223del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794772
|
GTGTGGGG others(9): Show |
G | 3 | a0001c0001t0001g0131a0001c0001t0001g0203a0001c0001t0004g0227 | 3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-236_476-221del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794772
|
GTGTGGGG others(11): Show |
G | 3 | a0001c0001t0001g0207a0001c0001t0001g0237a0001c0001t0001g0252 | 3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.476-236_476-219del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | ||||||
| chr6:154794773
|
T | G | 21 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(18): Show | 21 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.476-236T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794773 | ||||||
| chr6:154794775
|
T | G | 3 | a0001c0001t0002g0007a0001c0001t0006g0019a0001c0008t0002g0257 | 3 | HG03130.hp2 HG03540.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.476-234T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794775 | ||||||
| chr6:154794777
|
G | T | 53 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(50): Show | 53 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.476-232G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794777 | ||||||
| chr6:154794777
|
GGGGGTGT others(26): Show |
G | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.476-230_476-198del others(33): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794777 | |||||
| chr6:154794778
|
G | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476-231G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794778 | ||||||
| chr6:154794778
|
GGGGTGT | G | 11 | a0001c0001t0001g0124a0001c0001t0001g0192a0001c0001t0001g0206others(8): Show | 11 | HG00673.hp1 HG01081.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.476-229_476-224del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(1): Show |
G | 11 | a0001c0001t0001g0132a0001c0001t0001g0181a0001c0001t0001g0194others(8): Show | 11 | HG00408.hp2 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.476-229_476-222del others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(3): Show |
G | 5 | a0001c0001t0001g0096a0001c0001t0001g0182a0001c0001t0001g0189others(2): Show | 5 | HG02145.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-229_476-220del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(5): Show |
G | 1 | a0002c0004t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.476-229_476-218del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(7): Show |
G | 2 | a0001c0001t0002g0079a0006c0009t0001g0128 | 2 | HG02647.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.476-229_476-216del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(9): Show |
G | 3 | a0001c0001t0001g0169a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG02965.hp2 NA18971.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.476-229_476-214del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(11): Show |
G | 6 | a0001c0001t0001g0198a0001c0001t0001g0210a0001c0011t0001g0208others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-229_476-212del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.476-229_476-210del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(17): Show |
G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476-229_476-206del others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794778
|
GGGGTGTG others(27): Show |
G | 87 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.476-229_476-196del others(34): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | |||||
| chr6:154794779
|
G | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.476-230G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794779 | ||||||
| chr6:154794780
|
G | GGT | 11 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0014others(8): Show | 11 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.476-180_476-179dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.476-190_476-179dup others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
G | T | 10 | a0001c0001t0001g0099a0001c0001t0001g0199a0001c0001t0001g0204others(7): Show | 10 | HG00438.hp2 HG00609.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.476-229G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794780 | ||||||
| chr6:154794780
|
GGT | G | 12 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0093others(9): Show | 12 | HG00099.hp1 HG00741.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.476-180_476-179del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGT | G | 11 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0239others(8): Show | 11 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.476-182_476-179del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGT | G | 23 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0092others(20): Show | 23 | HG00642.hp2 HG01109.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.476-184_476-179del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0002g0046 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.476-188_476-179del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(5): Show |
G | 7 | a0001c0001t0002g0062a0001c0001t0002g0276a0001c0001t0002g0277others(4): Show | 7 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-190_476-179del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.476-198_476-179del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(17): Show |
G | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.476-202_476-179del others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(29): Show |
G | 1 | a0001c0001t0001g0241 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.476-214_476-179del others(36): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794780
|
GGTGTGTG others(31): Show |
G | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-216_476-179del others(38): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | |||||
| chr6:154794782
|
T | G | 6 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0029others(3): Show | 6 | HG02129.hp1 HG03540.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-227T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794782 | ||||||
| chr6:154794784
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.476-225T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794784 | ||||||
| chr6:154794785
|
GTGTGTGT others(10): Show |
G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.476-223_476-207del others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794785 | ||||||
| chr6:154794786
|
T | G | 1 | a0001c0001t0002g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.476-223T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794786 | ||||||
| chr6:154794787
|
GT | G | 3 | a0001c0001t0001g0129a0001c0001t0002g0075a0001c0001t0005g0196 | 3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-221delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794787 | ||||||
| chr6:154794788
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.476-221T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794788 | ||||||
| chr6:154794790
|
T | G | 3 | a0001c0001t0001g0129a0001c0001t0002g0075a0001c0001t0005g0196 | 3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-219T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794790 | ||||||
| chr6:154794792
|
T | G | 4 | a0001c0001t0001g0212a0001c0001t0002g0072a0001c0001t0002g0275others(1): Show | 4 | HG00621.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-217T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794792 | ||||||
| chr6:154794793
|
GT | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0203a0001c0001t0004g0227 | 3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-215delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794793 | ||||||
| chr6:154794794
|
T | G | 3 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0076 | 3 | HG01123.hp1 HG02080.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.476-215T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794794 | ||||||
| chr6:154794795
|
GT | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0212a0001c0001t0001g0237others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-213delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794795 | ||||||
| chr6:154794796
|
T | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0203a0001c0001t0004g0227 | 3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-213T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794796 | ||||||
| chr6:154794798
|
T | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0212a0001c0001t0001g0237others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-211T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794798 | ||||||
| chr6:154794800
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.476-209T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794800 | ||||||
| chr6:154794804
|
T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.476-205T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794804 | ||||||
| chr6:154794899
|
A | G | 2 | a0001c0001t0004g0197a0001c0001t0004g0221 | 2 | HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.476-110A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794899 | ||||||
| chr6:154794905
|
G | A | 2 | a0001c0001t0001g0172a0005c0005t0002g0256 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.476-104G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794905 | ||||||
| chr6:154795151
|
TTC | T | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.606+14_606+15delCT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154795151 | |||||
| chr6:154795495
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+356C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795495 | ||||||
| chr6:154795581
|
A | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+442A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795581 | ||||||
| chr6:154795765
|
C | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+626C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795765 | ||||||
| chr6:154795885
|
C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.606+746C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795885 | ||||||
| chr6:154796019
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.606+880T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796019 | ||||||
| chr6:154796177
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.606+1038G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796177 | ||||||
| chr6:154796280
|
T | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606+1141T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796280 | ||||||
| chr6:154796353
|
T | TTC | 11 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(8): Show | 11 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.606+1252_606+1253d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCC | 7 | a0001c0001t0001g0172a0001c0001t0001g0183a0001c0001t0001g0192others(4): Show | 7 | HG01167.hp1 HG01433.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+1216_606+1217i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCCTCT others(5): Show |
2 | a0001c0001t0001g0160a0001c0001t0007g0112 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.606+1216_606+1217i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCCTCT others(9): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG01070.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.606+1216_606+1217i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCCTCT others(15): Show |
1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCTCTC others(4): Show |
1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
T | TTCCTCTC others(6): Show |
1 | a0001c0001t0001g0138 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
TTC | T | 3 | a0001c0001t0001g0135a0001c0001t0002g0007a0001c0008t0002g0257 | 3 | HG01261.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.606+1252_606+1253d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
TTCTC | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0018others(2): Show | 5 | HG02273.hp2 HG02486.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+1250_606+1253d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
TTCTCTCT others(5): Show |
T | 1 | a0001c0001t0002g0053 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.606+1242_606+1253d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796353
|
TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0002g0022 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.606+1236_606+1253d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | |||||
| chr6:154796354
|
T | TCC | 9 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(6): Show | 9 | HG01515.hp2 HG01975.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1216_606+1217i others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796354 | |||||
| chr6:154796356
|
T | C | 158 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.606+1217T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796356 | ||||||
| chr6:154796358
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.606+1219T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796358 | ||||||
| chr6:154796385
|
C | CTCTGTCT others(1): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0211a0001c0001t0001g0226 | 3 | HG03098.hp1 HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.606+1249_606+1250i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796385 | |||||
| chr6:154796385
|
C | CTGTCTG | 26 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(23): Show | 26 | HG00609.hp2 HG01074.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.606+1247_606+1248i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796385 | |||||
| chr6:154796385
|
C | G | 15 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0135others(12): Show | 15 | HG01167.hp1 HG01261.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1246C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796385 | ||||||
| chr6:154796389
|
C | CTCTCTCT others(23): Show |
1 | a0001c0001t0008g0156 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(36): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606+1253_606+1254i others(30): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0101 | 2 | NA19062.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.606+1253_606+1254i others(28): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(17): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0108a0001c0001t0001g0245others(1): Show | 4 | HG02257.hp1 NA18942.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(15): Show |
9 | a0001c0001t0001g0071a0001c0001t0001g0145a0001c0001t0001g0174others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(13): Show |
14 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0086others(11): Show | 14 | HG00642.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(11): Show |
13 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0120others(10): Show | 13 | HG00735.hp1 HG01106.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(9): Show |
16 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0001g0095others(13): Show | 16 | HG00140.hp1 HG00544.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(3): Show |
2 | a0001c0001t0002g0275a0001c0012t0002g0279 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.606+1253_606+1254i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(7): Show |
15 | a0001c0001t0001g0064a0001c0001t0001g0085a0001c0001t0001g0102others(12): Show | 15 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.606+1253_606+1254i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(5): Show |
15 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0115others(12): Show | 15 | HG00609.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0127 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTGT others(3): Show |
6 | a0001c0001t0001g0105a0001c0001t0001g0157a0001c0001t0001g0168others(3): Show | 6 | HG00621.hp2 HG01123.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTCTGT others(7): Show |
1 | a0001c0001t0001g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTGTCT others(1): Show |
4 | a0001c0001t0001g0141a0002c0004t0001g0186a0002c0004t0001g0187others(1): Show | 4 | HG02145.hp1 HG02735.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+1257_606+1258i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTCTGTCT others(5): Show |
12 | a0001c0001t0001g0110a0001c0001t0001g0129a0001c0001t0001g0201others(9): Show | 12 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+1257_606+1258i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTG | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTGTCTG | 9 | a0001c0001t0001g0119a0001c0001t0001g0138a0001c0001t0001g0176others(6): Show | 9 | HG00597.hp2 HG01952.hp2 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | CTGTCTGT others(3): Show |
32 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0090others(29): Show | 32 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | |||||
| chr6:154796389
|
C | G | 52 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(49): Show | 52 | HG00609.hp2 HG01070.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.606+1250C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796389 | ||||||
| chr6:154796829
|
A | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.606+1690A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796829 | ||||||
| chr6:154796853
|
T | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606+1714T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796853 | ||||||
| chr6:154796873
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.606+1734G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796873 | ||||||
| chr6:154796881
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.606+1742A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796881 | ||||||
| chr6:154796890
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.606+1751T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796890 | ||||||
| chr6:154796953
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.606+1814C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796953 | ||||||
| chr6:154796980
|
C | CA | 12 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0111others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1854dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796980 | |||||
| chr6:154797105
|
ATTTTATA others(4790): Show |
A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG01261.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.606+1972_607-64del | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154797105 | |||||
| chr6:154797373
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0173 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.606+2234T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797373 | ||||||
| chr6:154797398
|
A | AT | 7 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+2269dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154797398 | |||||
| chr6:154797406
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.606+2267T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797406 | ||||||
| chr6:154797437
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.606+2298C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797437 | ||||||
| chr6:154797678
|
A | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.606+2539A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797678 | ||||||
| chr6:154797737
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.606+2598C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797737 | ||||||
| chr6:154798018
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.606+2879A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798018 | ||||||
| chr6:154798024
|
T | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606+2885T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798024 | ||||||
| chr6:154798166
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.606+3027T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798166 | ||||||
| chr6:154798392
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0173 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.606+3253T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798392 | ||||||
| chr6:154798594
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.607-3377C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798594 | ||||||
| chr6:154798903
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-3068G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798903 | ||||||
| chr6:154799126
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.607-2845C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799126 | ||||||
| chr6:154799317
|
T | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | NA18951.hp2 NA18993.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-2654T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799317 | ||||||
| chr6:154799379
|
A | G | 3 | a0001c0001t0001g0172a0001c0001t0002g0276a0001c0001t0002g0278 | 3 | HG02717.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.607-2592A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799379 | ||||||
| chr6:154799666
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.607-2305C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799666 | ||||||
| chr6:154799685
|
T | A | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.607-2286T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799685 | ||||||
| chr6:154799775
|
CTATT | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0132a0001c0001t0001g0235others(2): Show | 5 | HG01074.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-2173_607-2170d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154799775 | |||||
| chr6:154799775
|
CTATTTAT others(1): Show |
C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.607-2177_607-2170d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154799775 | |||||
| chr6:154800125
|
G | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.607-1846G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800125 | ||||||
| chr6:154800184
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.607-1787C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800184 | ||||||
| chr6:154800293
|
C | G | 2 | a0001c0001t0002g0200a0001c0001t0007g0112 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.607-1678C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800293 | ||||||
| chr6:154800355
|
A | G | 3 | a0001c0001t0005g0152a0001c0001t0005g0196a0001c0001t0005g0209 | 3 | HG03017.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.607-1616A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800355 | ||||||
| chr6:154800569
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.607-1402A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800569 | ||||||
| chr6:154800640
|
G | C | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.607-1331G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800640 | ||||||
| chr6:154800650
|
GT | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.607-1320delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800650 | ||||||
| chr6:154801040
|
G | C | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.607-931G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801040 | ||||||
| chr6:154801063
|
A | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.607-908A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801063 | ||||||
| chr6:154801178
|
A | G | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.607-793A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801178 | ||||||
| chr6:154801257
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.607-714A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801257 | ||||||
| chr6:154801504
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.607-467A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801504 | ||||||
| chr6:154801854
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.607-117G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801854 | ||||||
| chr6:154802254
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.783+107C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802254 | ||||||
| chr6:154802458
|
T | C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.783+311T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802458 | ||||||
| chr6:154802488
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783+341G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802488 | ||||||
| chr6:154802567
|
A | G | 1 | a0006c0009t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.783+420A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802567 | ||||||
| chr6:154802617
|
CA | C | 8 | a0001c0001t0001g0096a0001c0001t0001g0242a0001c0001t0001g0259others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+482delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 154802617 | |||||
| chr6:154802629
|
AT | A | 110 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.783+490delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 154802629 | |||||
| chr6:154802630
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+483T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802630 | ||||||
| chr6:154802637
|
T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783+490T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802637 | ||||||
| chr6:154802940
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.784-604C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802940 | ||||||
| chr6:154803032
|
G | T | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.784-512G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803032 | ||||||
| chr6:154803218
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.784-326A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803218 | ||||||
| chr6:154803328
|
A | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-216A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803328 | ||||||
| chr6:154803449
|
T | G | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.784-95T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803449 | ||||||
| chr6:154803481
|
A | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-63A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803481 | ||||||
| chr6:154803647
|
A | G | 1 | a0001c0001t0008g0156 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.863+24A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803647 | ||||||
| chr6:154803751
|
G | A | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+128G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803751 | ||||||
| chr6:154803775
|
C | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.863+152C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803775 | ||||||
| chr6:154804036
|
A | AT | 6 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.863+424dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | 154804036 | |||||
| chr6:154804219
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.863+596T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804219 | ||||||
| chr6:154804291
|
A | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+668A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804291 | ||||||
| chr6:154804383
|
C | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.863+760C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804383 | ||||||
| chr6:154804543
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.864-826C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804543 | ||||||
| chr6:154804856
|
T | C | 3 | a0002c0004t0001g0186a0002c0004t0001g0187a0002c0004t0001g0188 | 3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.864-513T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804856 | ||||||
| chr6:154804917
|
A | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.864-452A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804917 | ||||||
| chr6:154805009
|
G | A | 89 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.864-360G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805009 | ||||||
| chr6:154805107
|
C | T | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.864-262C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805107 | ||||||
| chr6:154805202
|
A | AT | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.864-167_864-166ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805202 | ||||||
| chr6:154805561
|
CT | C | 8 | a0001c0001t0001g0212a0001c0001t0001g0219a0001c0001t0002g0275others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+88delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 154805561 | |||||
| chr6:154805576
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.981+90A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805576 | ||||||
| chr6:154805720
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.981+234A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805720 | ||||||
| chr6:154805764
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.981+278T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805764 | ||||||
| chr6:154806035
|
G | T | 3 | a0001c0008t0002g0257a0005c0005t0002g0255a0005c0005t0002g0256 | 3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.981+549G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806035 | ||||||
| chr6:154806109
|
C | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.981+623C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806109 | ||||||
| chr6:154806323
|
G | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+837G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806323 | ||||||
| chr6:154806477
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.981+991G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806477 | ||||||
| chr6:154806506
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.981+1020G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806506 | ||||||
| chr6:154806802
|
T | TA | 4 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0037others(1): Show | 4 | HG01261.hp2 HG02300.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-1267dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 154806802 | |||||
| chr6:154806830
|
G | A | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.982-1240G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806830 | ||||||
| chr6:154806917
|
A | C | 1 | a0001c0001t0004g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.982-1153A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806917 | ||||||
| chr6:154807109
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.982-961T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807109 | ||||||
| chr6:154807198
|
G | C | 211 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.982-872G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807198 | ||||||
| chr6:154807292
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.982-778C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807292 | ||||||
| chr6:154807353
|
A | G | 1 | a0001c0001t0008g0156 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.982-717A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807353 | ||||||
| chr6:154807405
|
A | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.982-665A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807405 | ||||||
| chr6:154807450
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.982-620G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807450 | ||||||
| chr6:154807810
|
A | G | 169 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.982-260A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807810 | ||||||
| chr6:154807904
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.982-166A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807904 | ||||||
| chr6:154807969
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.982-101A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807969 | ||||||
| chr6:154808057
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.982-13A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154808057 | ||||||
| chr6:154808459
|
A | AT | 6 | a0001c0001t0002g0050a0001c0001t0003g0080a0001c0001t0003g0081others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-212dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | |||||
| chr6:154808459
|
AT | A | 181 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1114-212delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | |||||
| chr6:154808459
|
ATT | A | 11 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0107others(8): Show | 11 | HG02129.hp2 HG02723.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-213_1114-212d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | |||||
| chr6:154808511
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1114-175C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | chr6 | 154808511 | ||||||
| chr6:154808599
|
G | A | 1 | a0001c0001t0008g0156 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1114-87G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | chr6 | 154808599 | ||||||
| chr6:154808650
|
CCTTT | C | 209 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1114-33_1114-30del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808650 | |||||
| chr6:154809020
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0229 | 2 | NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1226+222A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809020 | ||||||
| chr6:154809134
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1226+336A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809134 | ||||||
| chr6:154809245
|
T | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1226+447T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809245 | ||||||
| chr6:154809250
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1226+452T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809250 | ||||||
| chr6:154809344
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1226+546C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809344 | ||||||
| chr6:154809550
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227-465A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809550 | ||||||
| chr6:154809633
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1227-382A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809633 | ||||||
| chr6:154809703
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1227-312A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809703 | ||||||
| chr6:154809844
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227-171G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809844 | ||||||
| chr6:154809955
|
G | A | 11 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(8): Show | 11 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227-60G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809955 | ||||||
| chr6:154810243
|
A | C | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+35A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810243 | ||||||
| chr6:154810344
|
T | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1420+136T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810344 | ||||||
| chr6:154810353
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1420+145C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810353 | ||||||
| chr6:154810358
|
TAGAG | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420+152_1420+155d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810358 | |||||
| chr6:154810365
|
GAGA | G | 80 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(77): Show | 80 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1420+166_1420+168d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810365 | |||||
| chr6:154810492
|
T | TA | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420+285dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810492 | |||||
| chr6:154810498
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+290G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810498 | ||||||
| chr6:154810513
|
T | C | 2 | a0003c0003t0002g0273a0003c0003t0002g0274 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1420+305T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810513 | ||||||
| chr6:154811048
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0238 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1420+840T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811048 | ||||||
| chr6:154811103
|
C | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1420+895C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811103 | ||||||
| chr6:154811179
|
T | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1420+971T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811179 | ||||||
| chr6:154811339
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1420+1131G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811339 | ||||||
| chr6:154811385
|
T | C | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1420+1177T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811385 | ||||||
| chr6:154811481
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1420+1273T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811481 | ||||||
| chr6:154811524
|
G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1420+1316G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811524 | ||||||
| chr6:154811883
|
G | A | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420+1675G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811883 | ||||||
| chr6:154811973
|
A | T | 3 | a0002c0004t0001g0186a0002c0004t0001g0187a0002c0004t0001g0188 | 3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1420+1765A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811973 | ||||||
| chr6:154811983
|
G | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+1775G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811983 | ||||||
| chr6:154812068
|
C | T | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+1860C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812068 | ||||||
| chr6:154812096
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1420+1888C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812096 | ||||||
| chr6:154812176
|
CT | C | 176 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1420+1991delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812176 | |||||
| chr6:154812176
|
CTT | C | 10 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0163others(7): Show | 10 | HG01517.hp1 HG02109.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420+1990_1420+199 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812176 | |||||
| chr6:154812199
|
T | A | 203 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1420+1991T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812199 | ||||||
| chr6:154812199
|
T | TA | 4 | a0001c0001t0002g0276a0001c0008t0002g0257a0003c0003t0002g0273others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+1994dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812199 | |||||
| chr6:154812263
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1420+2055A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812263 | ||||||
| chr6:154812289
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1420+2081C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812289 | ||||||
| chr6:154812292
|
C | CT | 52 | a0001c0001t0001g0086a0001c0001t0001g0111a0001c0001t0001g0120others(49): Show | 52 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1420+2105dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | |||||
| chr6:154812292
|
C | CTT | 6 | a0001c0001t0001g0143a0001c0001t0002g0029a0001c0001t0002g0033others(3): Show | 6 | HG00642.hp2 HG01978.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420+2104_1420+210 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | |||||
| chr6:154812292
|
CT | C | 24 | a0001c0001t0001g0195a0001c0001t0002g0073a0001c0001t0002g0075others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1420+2105delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | |||||
| chr6:154812337
|
G | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1420+2129G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812337 | ||||||
| chr6:154812413
|
G | C | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1420+2205G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812413 | ||||||
| chr6:154812546
|
C | G | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1420+2338C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812546 | ||||||
| chr6:154812608
|
C | G | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1420+2400C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812608 | ||||||
| chr6:154812735
|
A | G | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1420+2527A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812735 | ||||||
| chr6:154812797
|
T | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1420+2589T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812797 | ||||||
| chr6:154813022
|
G | C | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1421-2694G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813022 | ||||||
| chr6:154813039
|
CA | C | 218 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1421-2661delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154813039 | |||||
| chr6:154813080
|
T | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1421-2636T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813080 | ||||||
| chr6:154813272
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-2444C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813272 | ||||||
| chr6:154813273
|
C | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-2443C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813273 | ||||||
| chr6:154813297
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1421-2419G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813297 | ||||||
| chr6:154813492
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1421-2224T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813492 | ||||||
| chr6:154813523
|
C | T | 1 | a0001c0015t0001g0114 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1421-2193C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813523 | ||||||
| chr6:154813638
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1421-2078A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813638 | ||||||
| chr6:154813800
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1421-1916G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813800 | ||||||
| chr6:154813861
|
C | T | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1421-1855C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813861 | ||||||
| chr6:154813934
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1421-1782G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813934 | ||||||
| chr6:154813950
|
G | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1421-1766G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813950 | ||||||
| chr6:154814206
|
T | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1421-1510T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154814206 | ||||||
| chr6:154814391
|
A | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1421-1325A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154814391 | ||||||
| chr6:154815174
|
G | A | 11 | a0001c0001t0001g0198a0001c0001t0001g0203a0001c0001t0001g0207others(8): Show | 11 | HG02109.hp1 HG02630.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-542G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815174 | ||||||
| chr6:154815279
|
AGAGT | A | 10 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0181others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1421-433_1421-430d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154815279 | |||||
| chr6:154815293
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1421-423T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815293 | ||||||
| chr6:154815304
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1421-412T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815304 | ||||||
| chr6:154815329
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1421-387A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815329 | ||||||
| chr6:154815352
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1421-364G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815352 | ||||||
| chr6:154815367
|
G | T | 169 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1421-349G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815367 | ||||||
| chr6:154815399
|
T | C | 1 | a0001c0001t0002g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1421-317T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815399 | ||||||
| chr6:154815444
|
A | G | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1421-272A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815444 | ||||||
| chr6:154815953
|
G | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0189 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1521+137G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154815953 | ||||||
| chr6:154816002
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1521+186A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816002 | ||||||
| chr6:154816010
|
G | A | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1521+194G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816010 | ||||||
| chr6:154816139
|
T | C | 219 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1521+323T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816139 | ||||||
| chr6:154816236
|
T | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1521+420T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816236 | ||||||
| chr6:154816512
|
G | GCTGT | 214 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1521+699_1521+702d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154816512 | |||||
| chr6:154816521
|
C | T | 1 | a0001c0001t0003g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1521+705C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816521 | ||||||
| chr6:154816552
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1521+736A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816552 | ||||||
| chr6:154816825
|
A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1521+1009A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816825 | ||||||
| chr6:154816870
|
TTAAG | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0282 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1521+1058_1521+106 others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154816870 | |||||
| chr6:154817039
|
AT | A | 186 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1521+1227delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154817039 | |||||
| chr6:154817114
|
C | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1298C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817114 | ||||||
| chr6:154817115
|
C | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1299C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817115 | ||||||
| chr6:154817116
|
C | CTAGTGAT others(1): Show |
3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1300_1521+130 others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817116 | ||||||
| chr6:154817184
|
T | C | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1522-1295T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817184 | ||||||
| chr6:154817251
|
C | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01106.hp1 HG01261.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-1228C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817251 | ||||||
| chr6:154817676
|
G | A | 187 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1522-803G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817676 | ||||||
| chr6:154817715
|
A | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0032others(4): Show | 7 | HG01070.hp2 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1522-764A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817715 | ||||||
| chr6:154817808
|
T | C | 59 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0087others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1522-671T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817808 | ||||||
| chr6:154818110
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1522-369G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818110 | ||||||
| chr6:154818120
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1522-359A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818120 | ||||||
| chr6:154818257
|
CTAAT | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-220_1522-217d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154818257 | |||||
| chr6:154818397
|
A | G | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1522-82A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818397 | ||||||
| chr6:154818742
|
T | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635+150T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818742 | ||||||
| chr6:154818783
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1635+191G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818783 | ||||||
| chr6:154818806
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1635+214A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818806 | ||||||
| chr6:154818836
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1635+244A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818836 | ||||||
| chr6:154819083
|
G | GT | 187 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1635+498dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 154819083 | |||||
| chr6:154819092
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1635+500A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819092 | ||||||
| chr6:154819157
|
T | C | 224 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1635+565T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819157 | ||||||
| chr6:154819226
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1635+634T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819226 | ||||||
| chr6:154819468
|
A | G | 4 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278others(1): Show | 4 | HG03471.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636-709A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819468 | ||||||
| chr6:154819798
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1636-379G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819798 | ||||||
| chr6:154819834
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1636-343C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819834 | ||||||
| chr6:154819853
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1636-324G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819853 | ||||||
| chr6:154819871
|
C | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1636-306C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819871 | ||||||
| chr6:154820139
|
G | A | 2 | a0001c0001t0002g0035a0001c0014t0002g0052 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1636-38G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154820139 | ||||||
| chr6:154820517
|
A | T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792+184A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820517 | ||||||
| chr6:154820828
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1792+495C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820828 | ||||||
| chr6:154820889
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1792+556T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820889 | ||||||
| chr6:154820920
|
G | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+587G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820920 | ||||||
| chr6:154821010
|
A | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1792+677A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821010 | ||||||
| chr6:154821012
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792+679G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821012 | ||||||
| chr6:154821187
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1792+854C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821187 | ||||||
| chr6:154821231
|
G | A | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1792+898G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821231 | ||||||
| chr6:154821239
|
CCTGTTGG others(25): Show |
C | 6 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0164others(3): Show | 6 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+939_1792+970d others(34): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr6 | 154821239 | |||||
| chr6:154821331
|
T | C | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1793-945T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821331 | ||||||
| chr6:154821457
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1793-819G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821457 | ||||||
| chr6:154821460
|
A | G | 78 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0089others(75): Show | 78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1793-816A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821460 | ||||||
| chr6:154821478
|
C | G | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-798C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821478 | ||||||
| chr6:154821658
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1793-618A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821658 | ||||||
| chr6:154821774
|
G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1793-502G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821774 | ||||||
| chr6:154821818
|
G | A | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1793-458G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821818 | ||||||
| chr6:154821968
|
C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1793-308C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821968 | ||||||
| chr6:154821994
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1793-282C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821994 | ||||||
| chr6:154822148
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1793-128G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822148 | ||||||
| chr6:154822151
|
T | G | 27 | a0001c0001t0001g0094a0001c0001t0001g0199a0001c0001t0001g0202others(24): Show | 27 | HG00099.hp1 HG00609.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1793-125T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822151 | ||||||
| chr6:154822168
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1793-108G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822168 | ||||||
| chr6:154822545
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1926+136A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822545 | ||||||
| chr6:154822673
|
C | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0124others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1926+264C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822673 | ||||||
| chr6:154822935
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1926+526T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822935 | ||||||
| chr6:154823106
|
G | A | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1926+697G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823106 | ||||||
| chr6:154823136
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1926+727C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823136 | ||||||
| chr6:154823384
|
T | A | 1 | a0001c0011t0001g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1927-850T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823384 | ||||||
| chr6:154823639
|
GAGA | G | 4 | a0001c0001t0002g0275a0001c0001t0002g0280a0001c0001t0002g0281others(1): Show | 4 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1927-591_1927-589d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 154823639 | |||||
| chr6:154823751
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0248 | 2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1927-483A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823751 | ||||||
| chr6:154823827
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0264 | 2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1927-407A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823827 | ||||||
| chr6:154823883
|
C | T | 70 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(67): Show | 70 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1927-351C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823883 | ||||||
| chr6:154823907
|
T | A | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1927-327T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823907 | ||||||
| chr6:154823941
|
T | C | 17 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(14): Show | 17 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1927-293T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823941 | ||||||
| chr6:154824043
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1927-191A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154824043 | ||||||
| chr6:154824145
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1927-89T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154824145 | ||||||
| chr6:154824417
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2071+39A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824417 | ||||||
| chr6:154824429
|
G | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2071+51G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824429 | ||||||
| chr6:154824456
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2071+78A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824456 | ||||||
| chr6:154824482
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2071+104C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824482 | ||||||
| chr6:154824642
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2071+264T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824642 | ||||||
| chr6:154824804
|
G | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0252a0001c0011t0001g0208 | 3 | HG03098.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2071+426G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824804 | ||||||
| chr6:154824814
|
A | G | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2071+436A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824814 | ||||||
| chr6:154824836
|
G | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2071+458G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824836 | ||||||
| chr6:154824957
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2071+579A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824957 | ||||||
| chr6:154824961
|
G | GA | 22 | a0001c0001t0001g0090a0001c0001t0001g0271a0001c0001t0002g0072others(19): Show | 22 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.2071+595dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154824961 | |||||
| chr6:154825099
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2071+721T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825099 | ||||||
| chr6:154825129
|
T | A | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2071+751T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825129 | ||||||
| chr6:154825137
|
G | C | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2071+759G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825137 | ||||||
| chr6:154825178
|
A | G | 6 | a0001c0001t0002g0200a0001c0001t0003g0080a0001c0001t0003g0081others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071+800A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825178 | ||||||
| chr6:154825241
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2071+863T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825241 | ||||||
| chr6:154825401
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2071+1023A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825401 | ||||||
| chr6:154825655
|
C | CA | 35 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0109others(32): Show | 35 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.2071+1298dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | |||||
| chr6:154825655
|
C | CAA | 138 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.2071+1297_2071+129 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | |||||
| chr6:154825655
|
C | CAAA | 26 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0104others(23): Show | 26 | HG00544.hp1 HG00735.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2071+1296_2071+129 others(7): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | |||||
| chr6:154825655
|
C | CAAAA | 14 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0076others(11): Show | 14 | HG00621.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2071+1295_2071+129 others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | |||||
| chr6:154825693
|
C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2071+1315C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825693 | ||||||
| chr6:154825852
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2072-1320G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825852 | ||||||
| chr6:154826021
|
A | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0122others(2): Show | 5 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072-1151A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826021 | ||||||
| chr6:154826272
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2072-900A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826272 | ||||||
| chr6:154826706
|
G | A | 4 | a0001c0013t0002g0106a0003c0003t0002g0272a0003c0003t0002g0273others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2072-466G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826706 | ||||||
| chr6:154826708
|
T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2072-464T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826708 | ||||||
| chr6:154826745
|
G | A | 62 | a0001c0001t0001g0135a0001c0001t0002g0001a0001c0001t0002g0002others(59): Show | 62 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2072-427G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826745 | ||||||
| chr6:154826849
|
T | C | 4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2072-323T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826849 | ||||||
| chr6:154826864
|
A | T | 1 | a0003c0003t0002g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2072-308A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826864 | ||||||
| chr6:154826993
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2072-179T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826993 | ||||||
| chr6:154827048
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0236 | 2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2072-124T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154827048 | ||||||
| chr6:154827129
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2072-43A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154827129 | ||||||
| chr6:154827250
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2140+10C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827250 | ||||||
| chr6:154827482
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2140+242G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827482 | ||||||
| chr6:154827719
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2140+479T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827719 | ||||||
| chr6:154827834
|
C | CG | 95 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(92): Show | 95 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2140+605dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | |||||
| chr6:154827834
|
C | CGG | 34 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0166others(31): Show | 34 | HG00597.hp1 HG00642.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2140+604_2140+605d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | |||||
| chr6:154827834
|
CG | C | 18 | a0001c0001t0001g0098a0001c0001t0001g0125a0001c0001t0001g0164others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.2140+605delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | |||||
| chr6:154827839
|
G | A | 1 | a0001c0013t0002g0106 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2140+599G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | ||||||
| chr6:154827839
|
G | C | 1 | a0006c0009t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2140+599G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | ||||||
| chr6:154827839
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0002g0013 | 2 | HG00733.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2140+599G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | ||||||
| chr6:154827844
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2140+604G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827844 | ||||||
| chr6:154828069
|
T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2140+829T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828069 | ||||||
| chr6:154828131
|
A | G | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140+891A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828131 | ||||||
| chr6:154828345
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2140+1105C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828345 | ||||||
| chr6:154828369
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2140+1129A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828369 | ||||||
| chr6:154828496
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2140+1256A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828496 | ||||||
| chr6:154828562
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2140+1322G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828562 | ||||||
| chr6:154828809
|
A | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(58): Show | 61 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2140+1569A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828809 | ||||||
| chr6:154828922
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2140+1682A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828922 | ||||||
| chr6:154828971
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2140+1731T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828971 | ||||||
| chr6:154828993
|
C | CT | 16 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140+1762dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154828993 | |||||
| chr6:154829195
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2141-1727T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829195 | ||||||
| chr6:154829214
|
G | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(63): Show | 66 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2141-1708G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829214 | ||||||
| chr6:154829232
|
A | AT | 59 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(56): Show | 59 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.2141-1674dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829232 | |||||
| chr6:154829232
|
AT | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0183others(3): Show | 6 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2141-1674delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829232 | |||||
| chr6:154829497
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2141-1425C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829497 | ||||||
| chr6:154829573
|
T | C | 4 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-1349T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829573 | ||||||
| chr6:154829610
|
A | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(63): Show | 66 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2141-1312A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829610 | ||||||
| chr6:154829629
|
G | A | 19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.2141-1293G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829629 | ||||||
| chr6:154829781
|
C | CCTGTAAT others(8): Show |
1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2141-1138_2141-112 others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829781 | |||||
| chr6:154829781
|
C | T | 2 | a0005c0005t0002g0255a0005c0005t0002g0256 | 2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2141-1141C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829781 | ||||||
| chr6:154830125
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2141-797C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154830125 | ||||||
| chr6:154830640
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2141-282T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154830640 | ||||||
| chr6:154831177
|
C | G | 67 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(64): Show | 67 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.2359+37C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831177 | ||||||
| chr6:154831230
|
A | G | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2359+90A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831230 | ||||||
| chr6:154831255
|
C | CT | 11 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(8): Show | 11 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2359+124dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831255 | |||||
| chr6:154831442
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2359+302A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831442 | ||||||
| chr6:154831567
|
A | G | 3 | a0003c0003t0002g0272a0003c0003t0002g0273a0003c0003t0002g0274 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2360-372A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831567 | ||||||
| chr6:154831637
|
T | TTCTAAGC others(1): Show |
4 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-300_2360-293d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831637 | |||||
| chr6:154831646
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0204a0001c0001t0001g0216others(1): Show | 4 | HG00609.hp2 HG02040.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-293T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831646 | ||||||
| chr6:154831692
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360-247A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831692 | ||||||
| chr6:154831703
|
T | TA | 16 | a0001c0001t0001g0066a0001c0001t0001g0103a0001c0001t0001g0116others(13): Show | 16 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2360-197dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
T | TAA | 12 | a0001c0001t0001g0064a0001c0001t0001g0145a0001c0001t0001g0160others(9): Show | 12 | HG00099.hp1 HG00673.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-198_2360-197d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
T | TAAA | 12 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0089others(9): Show | 12 | HG01358.hp1 HG02922.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.2360-199_2360-197d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2360-213_2360-197d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2360-225_2360-197d others(31): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TA | T | 14 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0104others(11): Show | 14 | HG00099.hp2 HG00558.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2360-197delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAA | T | 12 | a0001c0001t0001g0071a0001c0001t0001g0099a0001c0001t0001g0111others(9): Show | 12 | HG00558.hp1 HG01070.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-198_2360-197d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAA | T | 10 | a0001c0001t0001g0121a0001c0001t0001g0171a0001c0001t0001g0181others(7): Show | 10 | HG01516.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2360-200_2360-197d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAA | T | 8 | a0001c0001t0001g0096a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG01516.hp1 HG01517.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-201_2360-197d others(7): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0246others(5): Show | 8 | HG01361.hp2 HG01433.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2360-204_2360-197d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(2): Show |
T | 8 | a0001c0001t0002g0024a0001c0001t0002g0038a0001c0001t0002g0076others(5): Show | 8 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-205_2360-197d others(11): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(3): Show |
T | 61 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0002g0001others(58): Show | 61 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2360-206_2360-197d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(4): Show |
T | 21 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0097others(18): Show | 21 | HG00408.hp1 HG00621.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2360-207_2360-197d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(5): Show |
T | 44 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0087others(41): Show | 44 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.2360-208_2360-197d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0001g0108a0001c0001t0001g0180 | 2 | HG00597.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2360-209_2360-197d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(7): Show |
T | 1 | a0002c0004t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2360-210_2360-197d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0002g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2360-213_2360-197d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2360-214_2360-197d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(13): Show |
T | 5 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-216_2360-197d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831703
|
TAAAAAAA others(22): Show |
T | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2360-225_2360-197d others(31): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | |||||
| chr6:154831705
|
A | T | 1 | a0001c0001t0007g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360-234A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831705 | ||||||
| chr6:154831843
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2360-96C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831843 |