Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57466 |
| ensemblid | ENSG00000156304.15 |
| hgncid | 19304 |
| symbol | SCAF4 |
| name | SR-related CTD associated factor 4 |
| refseq_nuc | NM_020706.2 |
| refseq_prot | NP_065757.1 |
| ensembl_nuc | ENST00000286835.12 |
| ensembl_prot | ENSP00000286835.7 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 31671000 |
| end | 31732118 |
| strand | - |
| ver | v1.2 |
| region | chr21:31671000-31732118 |
| region5000 | chr21:31666000-31737118 |
| regionname0 | SCAF4_chr21_31671000_31732118 |
| regionname5000 | SCAF4_chr21_31666000_31737118 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1147 | 344 | 75 | 72 | 147 | 10 | 38 | 117 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0002 | 0/0 | 1147 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0003 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0004 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0005 | 0/0 | 1147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0006 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| a0007 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | MDAVN others(1142): Show |
chr21 | 31666000 | 31737118 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3441 | 269 | 44 | 53 | 130 | 9 | 31 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0002 | 0/0 | 3441 | 42 | 11 | 8 | 15 | 1 | 7 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0003 | 0/0 | 3441 | 13 | 11 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0004 | 0/0 | 3441 | 9 | 7 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0005 | 0/0 | 3441 | 3 | 0 | 3 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0007 | 0/0 | 3441 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0008 | 0/0 | 3441 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0009 | 0/0 | 3441 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0011 | 0/0 | 3441 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0013 | 0/0 | 3441 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0001c0017 | 0/0 | 3441 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0002c0006 | 0/0 | 3441 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0003c0014 | 0/0 | 3441 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0004c0016 | 0/0 | 3441 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0005c0015 | 0/0 | 3441 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0006c0012 | 0/0 | 3441 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 | ||
| a0007c0010 | 0/0 | 3441 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | ATGGA others(3436): Show |
chr21 | 31666000 | 31737118 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4269 | 241 | 42 | 46 | 118 | 8 | 25 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0001t0002 | 0/0 | 4268 | 12 | 1 | 1 | 10 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4263): Show |
chr21 | 31666000 | 31737118 |
| a0001c0001t0003 | 0/0 | 4265 | 10 | 0 | 5 | 0 | 0 | 5 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4260): Show |
chr21 | 31666000 | 31737118 |
| a0001c0001t0004 | 0/0 | 4270 | 5 | 0 | 1 | 2 | 1 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4265): Show |
chr21 | 31666000 | 31737118 |
| a0001c0001t0005 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4265): Show |
chr21 | 31666000 | 31737118 |
| a0001c0002t0001 | 0/0 | 4269 | 37 | 10 | 5 | 14 | 1 | 7 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0002t0002 | 0/0 | 4268 | 2 | 1 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4263): Show |
chr21 | 31666000 | 31737118 |
| a0001c0002t0004 | 0/0 | 4270 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4265): Show |
chr21 | 31666000 | 31737118 |
| a0001c0002t0006 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0002t0007 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGTT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0003t0001 | 0/0 | 4269 | 9 | 8 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0003t0002 | 0/0 | 4268 | 4 | 3 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4263): Show |
chr21 | 31666000 | 31737118 |
| a0001c0004t0001 | 0/0 | 4269 | 9 | 7 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0005t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0005t0002 | 0/0 | 4268 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4263): Show |
chr21 | 31666000 | 31737118 |
| a0001c0007t0001 | 0/0 | 4269 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0008t0001 | 0/0 | 4269 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0009t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0011t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0013t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0001c0017t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0002c0006t0001 | 0/0 | 4269 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0003c0014t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0004c0016t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0005c0015t0001 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0006c0012t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| a0007c0010t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | AGGGT others(4264): Show |
chr21 | 31666000 | 31737118 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0006g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0007g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0007t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0007t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0008t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0008t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0009t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0011t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0013t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0017t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0003c0014t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0004c0016t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0005c0015t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0006c0012t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0007c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0190 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00738 | hp1 | a0001 | c0005 | t0002 | g0341 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00741 | hp1 | a0001 | c0008 | t0001 | g0208 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0142 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01074 | hp2 | a0002 | c0006 | t0001 | g0271 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0340 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01106 | hp2 | a0001 | c0008 | t0001 | g0164 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0140 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01243 | hp2 | a0002 | c0006 | t0001 | g0322 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01261 | hp2 | a0001 | c0005 | t0002 | g0339 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01346 | hp1 | a0001 | c0002 | t0007 | g0343 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0218 | EUR | IBS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01934 | hp1 | a0001 | c0013 | t0001 | g0284 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01934 | hp2 | a0001 | c0002 | t0006 | g0342 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0121 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02071 | hp1 | a0003 | c0014 | t0001 | g0114 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02135 | hp2 | a0004 | c0016 | t0001 | g0297 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0002 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0187 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02970 | hp1 | a0001 | c0011 | t0001 | g0321 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0119 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0127 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0323 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03492 | hp2 | a0005 | c0015 | t0001 | g0025 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0189 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0328 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03710 | hp1 | a0002 | c0006 | t0001 | g0304 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0333 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18974 | hp1 | a0001 | c0007 | t0001 | g0319 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18980 | hp1 | a0001 | c0007 | t0001 | g0296 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19086 | hp1 | a0006 | c0012 | t0001 | g0048 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ASW | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0210 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0002 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03471 | hp2 | a0001 | c0017 | t0001 | g0149 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA21309 | hp2 | a0007 | c0010 | t0001 | g0145 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0235 | REF | REF | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0155 | REF | REF | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671418 | G | A | 1 | a0006 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.3425C>T | p.Ala1142Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3851/4269 | 3425/3444 | 1142/1147 | chr21 | 31671418 | |||
| chr21:31671571 | T | C | 1 | a0003 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.3272A>G | p.Lys1091Arg | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3698/4269 | 3272/3444 | 1091/1147 | chr21 | 31671571 | |||
| chr21:31693399 | G | A | 1 | a0005 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1408C>T | p.Arg470Cys | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/20 | 1834/4269 | 1408/3444 | 470/1147 | chr21 | 31693399 | |||
| chr21:31694928 | G | C | 1 | a0004 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1121C>G | p.Pro374Arg | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/20 | 1547/4269 | 1121/3444 | 374/1147 | chr21 | 31694928 | |||
| chr21:31696624 | C | A | 1 | a0002 | 3 | HG01074.hp2 HG01243.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.904G>T | p.Val302Leu | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1330/4269 | 904/3444 | 302/1147 | chr21 | 31696624 | |||
| chr21:31696683 | G | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.845C>A | p.Thr282Asn | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1271/4269 | 845/3444 | 282/1147 | chr21 | 31696683 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671507 | C | A | 1 | a0001c0013 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.3336G>T | p.Gly1112Gly | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3762/4269 | 3336/3444 | 1112/1147 | chr21 | 31671507 | |||
| chr21:31672065 | G | A | 1 | a0001c0008 | 2 | HG00741.hp1 HG01106.hp2 |
synonymous_variant | LOW | c.2778C>T | p.Gly926Gly | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3204/4269 | 2778/3444 | 926/1147 | chr21 | 31672065 | |||
| chr21:31672095 | A | G | 1 | a0001c0005 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.2748T>C | p.Val916Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3174/4269 | 2748/3444 | 916/1147 | chr21 | 31672095 | |||
| chr21:31685432 | A | C | 1 | a0001c0017 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2262T>G | p.Pro754Pro | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 18/20 | 2688/4269 | 2262/3444 | 754/1147 | chr21 | 31685432 | |||
| chr21:31685671 | A | C | 1 | a0001c0011 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2106T>G | p.Pro702Pro | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/20 | 2532/4269 | 2106/3444 | 702/1147 | chr21 | 31685671 | |||
| chr21:31693373 | A | G | 2 | a0001c0003 a0001c0011 |
14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
synonymous_variant | LOW | c.1434T>C | p.Ser478Ser | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/20 | 1860/4269 | 1434/3444 | 478/1147 | chr21 | 31693373 | |||
| chr21:31696649 | T | C | 4 | a0001c0002 a0001c0008 a0001c0009 others(1): Show |
46 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
synonymous_variant | LOW | c.879A>G | p.Ala293Ala | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1305/4269 | 879/3444 | 293/1147 | chr21 | 31696649 | |||
| chr21:31702320 | A | G | 2 | a0001c0008 a0001c0009 |
3 | HG00741.hp1 HG01070.hp2 HG01106.hp2 |
synonymous_variant | LOW | c.381T>C | p.Ile127Ile | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/20 | 807/4269 | 381/3444 | 127/1147 | chr21 | 31702320 | |||
| chr21:31702353 | A | C | 1 | a0001c0004 | 9 | HG00639.hp2 HG01175.hp2 HG01891.hp2 others(6): Show |
synonymous_variant | LOW | c.348T>G | p.Leu116Leu | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/20 | 774/4269 | 348/3444 | 116/1147 | chr21 | 31702353 | |||
| chr21:31703906 | A | C | 1 | a0001c0007 | 2 | NA18974.hp1 NA18980.hp1 |
synonymous_variant | LOW | c.180T>G | p.Val60Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/20 | 606/4269 | 180/3444 | 60/1147 | chr21 | 31703906 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671108 | T | TA | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 |
7 | HG01109.hp2 HG01361.hp2 HG01515.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*290dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 290 | chr21 | 31671108 | ||||||
| chr21:31671108 | TA | T | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(1): Show |
20 | HG00738.hp1 HG01106.hp1 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*290delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 290 | chr21 | 31671108 | ||||||
| chr21:31671126 | TAGAG | T | 1 | a0001c0001t0003 | 10 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*269_*272delCTCT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 269 | chr21 | 31671126 | ||||||
| chr21:31671130 | G | A | 1 | a0001c0003t0001 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 269 | chr21 | 31671130 | ||||||
| chr21:31671366 | G | A | 1 | a0001c0001t0005 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 33 | chr21 | 31671366 | ||||||
| chr21:31732035 | G | C | 1 | a0001c0002t0006 | 1 | HG01934.hp2 | 5_prime_UTR_variant | MODIFIER | c.-343C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/20 | 343 | chr21 | 31732035 | ||||||
| chr21:31732115 | C | A | 1 | a0001c0002t0007 | 1 | HG01346.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-423G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/20 | chr21 | 31732115 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31672507 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(100): Show |
105 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2489-153T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672507 | |||||||
| chr21:31672943 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-589C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672943 | |||||||
| chr21:31672945 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-591A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672945 | |||||||
| chr21:31673251 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2489-897A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673251 | |||||||
| chr21:31673403 | G | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-1049C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673403 | |||||||
| chr21:31673471 | A | ATACTTTA others(672): Show |
6 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0005t0001g0340 others(3): Show |
7 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.2489-1118_2489-111 others(683): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673471 | |||||||
| chr21:31673471 | A | ATACTTTA others(672): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-1118_2489-111 others(683): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673471 | |||||||
| chr21:31673520 | G | A | 5 | a0001c0001t0001g0253 a0001c0002t0001g0157 a0001c0002t0001g0158 others(2): Show |
5 | HG02523.hp2 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489-1166C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673520 | |||||||
| chr21:31673842 | C | T | 1 | a0001c0003t0002g0002 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-1488G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673842 | |||||||
| chr21:31673903 | TA | T | 6 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0005t0001g0340 others(3): Show |
7 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.2489-1550delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673903 | |||||||
| chr21:31673921 | A | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(335): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.2489-1567T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673921 | |||||||
| chr21:31673970 | T | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.2489-1616A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673970 | |||||||
| chr21:31673987 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2489-1633C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673987 | |||||||
| chr21:31674208 | A | C | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2489-1854T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674208 | |||||||
| chr21:31674404 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2489-2050G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674404 | |||||||
| chr21:31674681 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-2327G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674681 | |||||||
| chr21:31674692 | T | C | 9 | a0001c0001t0001g0244 a0001c0001t0001g0256 a0001c0001t0001g0268 others(6): Show |
9 | HG02015.hp1 HG02165.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-2338A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674692 | |||||||
| chr21:31674751 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-2397C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674751 | |||||||
| chr21:31674786 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0222 |
2 | HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2489-2432A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674786 | |||||||
| chr21:31674822 | A | AT | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG00099.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2489-2469dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674822 | |||||||
| chr21:31674851 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2489-2497A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674851 | |||||||
| chr21:31674875 | G | T | 1 | a0001c0001t0003g0153 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2489-2521C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674875 | |||||||
| chr21:31675004 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-2650A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675004 | |||||||
| chr21:31675005 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2489-2651A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675005 | |||||||
| chr21:31675046 | A | C | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2489-2692T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675046 | |||||||
| chr21:31675067 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2489-2713A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675067 | |||||||
| chr21:31675234 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489-2880T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675234 | |||||||
| chr21:31675235 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-2881A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675235 | |||||||
| chr21:31675508 | T | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.2489-3154A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675508 | |||||||
| chr21:31675645 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2489-3291C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675645 | |||||||
| chr21:31675702 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-3348C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675702 | |||||||
| chr21:31675828 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2489-3474T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675828 | |||||||
| chr21:31675883 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2489-3529G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675883 | |||||||
| chr21:31675909 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0225 |
4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489-3555C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675909 | |||||||
| chr21:31675919 | T | C | 2 | a0001c0001t0001g0172 a0001c0003t0002g0127 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2489-3565A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675919 | |||||||
| chr21:31675922 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2489-3568C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675922 | |||||||
| chr21:31675948 | C | T | 3 | a0001c0001t0001g0250 a0001c0008t0001g0164 a0001c0008t0001g0208 |
3 | HG00140.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2489-3594G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675948 | |||||||
| chr21:31676003 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(9): Show |
13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2489-3649A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676003 | |||||||
| chr21:31676044 | A | C | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2489-3690T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676044 | |||||||
| chr21:31676100 | G | C | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-3746C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676100 | |||||||
| chr21:31676230 | G | A | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-3876C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676230 | |||||||
| chr21:31676493 | G | C | 1 | a0001c0008t0001g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2489-4139C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676493 | |||||||
| chr21:31676551 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.2489-4197A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676551 | |||||||
| chr21:31676592 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2489-4238G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676592 | |||||||
| chr21:31676865 | ATCTG | A | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-4515_2489-451 others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676865 | |||||||
| chr21:31676940 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2489-4586C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676940 | |||||||
| chr21:31677077 | C | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2489-4723G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677077 | |||||||
| chr21:31677154 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-4800G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677154 | |||||||
| chr21:31677404 | T | C | 1 | a0001c0002t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2489-5050A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677404 | |||||||
| chr21:31677476 | C | T | 4 | a0001c0002t0001g0015 a0001c0002t0001g0203 a0001c0002t0001g0209 others(1): Show |
4 | HG02602.hp1 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489-5122G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677476 | |||||||
| chr21:31677579 | A | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2489-5225T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677579 | |||||||
| chr21:31677649 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2489-5295G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677649 | |||||||
| chr21:31677677 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2489-5323G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677677 | |||||||
| chr21:31677803 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-5449A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677803 | |||||||
| chr21:31677816 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2489-5462G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677816 | |||||||
| chr21:31677826 | T | C | 1 | a0001c0008t0001g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2489-5472A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677826 | |||||||
| chr21:31677972 | T | TACCTTAG others(4): Show |
1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2489-5629_2489-561 others(15): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677972 | |||||||
| chr21:31677974 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0004g0275 |
2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.2489-5620G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677974 | |||||||
| chr21:31678005 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2489-5651G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678005 | |||||||
| chr21:31678162 | T | C | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-5808A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678162 | |||||||
| chr21:31678264 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0088 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2489-5910T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678264 | |||||||
| chr21:31678390 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2489-6036T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678390 | |||||||
| chr21:31678406 | C | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0216 |
2 | HG01074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2489-6052G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678406 | |||||||
| chr21:31678472 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2489-6118A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678472 | |||||||
| chr21:31678520 | T | TAAAAACT others(318): Show |
3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-6167_2489-616 others(329): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678520 | |||||||
| chr21:31678621 | T | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2489-6267A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678621 | |||||||
| chr21:31679098 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+5951C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679098 | |||||||
| chr21:31679211 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0112 others(85): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2488+5838A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679211 | |||||||
| chr21:31679338 | GGTTT | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2488+5707_2488+571 others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679338 | |||||||
| chr21:31679502 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(96): Show |
101 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2488+5547A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679502 | |||||||
| chr21:31679683 | GAT | G | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+5364_2488+536 others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679683 | |||||||
| chr21:31680385 | T | C | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2488+4664A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680385 | |||||||
| chr21:31680834 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2488+4215A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680834 | |||||||
| chr21:31680915 | C | T | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+4134G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680915 | |||||||
| chr21:31681328 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2488+3721G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681328 | |||||||
| chr21:31681547 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(105): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2488+3502A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681547 | |||||||
| chr21:31681567 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(105): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2488+3482C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681567 | |||||||
| chr21:31681674 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2488+3375A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681674 | |||||||
| chr21:31681762 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2488+3287A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681762 | |||||||
| chr21:31681796 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2488+3253C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681796 | |||||||
| chr21:31681994 | T | C | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+3055A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681994 | |||||||
| chr21:31682103 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2488+2946A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682103 | |||||||
| chr21:31682213 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2488+2836A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682213 | |||||||
| chr21:31682214 | A | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG00423.hp2 HG02074.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2488+2835T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682214 | |||||||
| chr21:31682231 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(16): Show |
21 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.2488+2818G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682231 | |||||||
| chr21:31682250 | G | A | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+2799C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682250 | |||||||
| chr21:31682251 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0084 |
2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2488+2798G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682251 | |||||||
| chr21:31682313 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0225 |
4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2488+2736T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682313 | |||||||
| chr21:31682376 | C | CA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
100 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2488+2672dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682376 | |||||||
| chr21:31682414 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+2635T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682414 | |||||||
| chr21:31682448 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
239 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2488+2601C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682448 | |||||||
| chr21:31682551 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+2498G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682551 | |||||||
| chr21:31682812 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2488+2237G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682812 | |||||||
| chr21:31682822 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2488+2227C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682822 | |||||||
| chr21:31682900 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2488+2149A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682900 | |||||||
| chr21:31683120 | C | T | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+1929G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683120 | |||||||
| chr21:31683342 | C | T | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+1707G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683342 | |||||||
| chr21:31683444 | A | C | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(1): Show |
4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+1605T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683444 | |||||||
| chr21:31683467 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2488+1582G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683467 | |||||||
| chr21:31683628 | C | A | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+1421G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683628 | |||||||
| chr21:31683668 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2488+1381C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683668 | |||||||
| chr21:31683709 | G | GA | 10 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(7): Show |
10 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2488+1339dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683709 | |||||||
| chr21:31684027 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2488+1022A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684027 | |||||||
| chr21:31684152 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+897T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684152 | |||||||
| chr21:31684260 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
240 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2488+789C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684260 | |||||||
| chr21:31684374 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+675T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684374 | |||||||
| chr21:31684423 | C | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0134 a0001c0001t0001g0135 others(16): Show |
20 | HG00140.hp2 HG01099.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.2488+626G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684423 | |||||||
| chr21:31684499 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+550A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684499 | |||||||
| chr21:31684523 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2488+526C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684523 | |||||||
| chr21:31684546 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(1): Show |
4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+503C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684546 | |||||||
| chr21:31684616 | G | T | 1 | a0001c0002t0001g0157 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2488+433C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684616 | |||||||
| chr21:31684617 | T | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2488+432A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684617 | |||||||
| chr21:31684850 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2488+199A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684850 | |||||||
| chr21:31684981 | T | C | 5 | a0001c0001t0001g0258 a0001c0001t0001g0287 a0001c0001t0001g0290 others(2): Show |
5 | NA18943.hp2 NA18946.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488+68A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684981 | |||||||
| chr21:31684999 | T | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0246 a0001c0008t0001g0208 |
3 | HG00741.hp1 HG03831.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2488+50A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684999 | |||||||
| chr21:31684999 | TG | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2488+49delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684999 | |||||||
| chr21:31685000 | G | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0246 a0001c0008t0001g0208 |
3 | HG00741.hp1 HG03831.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2488+49C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685000 | |||||||
| chr21:31685001 | G | A | 1 | a0001c0003t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2488+48C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685001 | |||||||
| chr21:31685003 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0002g0282 |
2 | NA18955.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2488+46C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685003 | |||||||
| chr21:31685014 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+35C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685014 | |||||||
| chr21:31685495 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2210-11T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685495 | |||||||
| chr21:31685529 | C | T | 1 | a0001c0007t0001g0296 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2209+39G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685529 | |||||||
| chr21:31685539 | A | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2209+29T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685539 | |||||||
| chr21:31685547 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2209+21A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685547 | |||||||
| chr21:31685762 | C | T | 3 | a0001c0002t0001g0141 a0001c0002t0001g0176 a0001c0002t0001g0226 |
3 | HG01109.hp1 HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2044-29G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31685762 | |||||||
| chr21:31685863 | T | C | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-130A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31685863 | |||||||
| chr21:31686151 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2044-418G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686151 | |||||||
| chr21:31686203 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2044-485_2044-471d others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686203 | |||||||
| chr21:31686214 | AAAG | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
10 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2044-484_2044-482d others(5): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686214 | |||||||
| chr21:31686215 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(105): Show |
110 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.2044-482T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686215 | |||||||
| chr21:31686216 | AG | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(100): Show |
105 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.2044-484delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686216 | |||||||
| chr21:31686217 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0062 others(2): Show |
5 | HG01243.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-484C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686217 | |||||||
| chr21:31686217 | GA | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0178 a0001c0001t0001g0250 others(3): Show |
6 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-485delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686217 | |||||||
| chr21:31686218 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
10 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2044-485T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686218 | |||||||
| chr21:31686231 | A | G | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(1): Show |
4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044-498T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686231 | |||||||
| chr21:31686258 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(8): Show |
13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2044-525G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686258 | |||||||
| chr21:31686364 | C | T | 338 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(335): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.2044-631G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686364 | |||||||
| chr21:31686407 | A | G | 6 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(3): Show |
6 | HG01952.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-674T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686407 | |||||||
| chr21:31686430 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
123 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.2044-697G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686430 | |||||||
| chr21:31686566 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044-833C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686566 | |||||||
| chr21:31686669 | C | T | 1 | a0001c0003t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2044-936G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686669 | |||||||
| chr21:31686735 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
242 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.2044-1002T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686735 | |||||||
| chr21:31686853 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(8): Show |
13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2044-1120A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686853 | |||||||
| chr21:31686920 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2044-1187G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686920 | |||||||
| chr21:31687160 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2043+1147G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687160 | |||||||
| chr21:31687184 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 |
3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2043+1123G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687184 | |||||||
| chr21:31687230 | A | C | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043+1077T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687230 | |||||||
| chr21:31687259 | G | A | 1 | a0002c0006t0001g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2043+1048C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687259 | |||||||
| chr21:31687276 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
124 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2043+1031G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687276 | |||||||
| chr21:31687316 | T | C | 1 | a0001c0003t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2043+991A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687316 | |||||||
| chr21:31687518 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2043+789A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687518 | |||||||
| chr21:31687701 | CA | C | 46 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(43): Show |
46 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2043+605delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687701 | |||||||
| chr21:31687716 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2043+591T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687716 | |||||||
| chr21:31687836 | G | A | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+471C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687836 | |||||||
| chr21:31687873 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2043+434G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687873 | |||||||
| chr21:31688060 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2043+247A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688060 | |||||||
| chr21:31688114 | C | CA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2043+192dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAA | 68 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0133 others(65): Show |
68 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2043+191_2043+192d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAA | 35 | a0001c0001t0001g0137 a0001c0001t0001g0154 a0001c0001t0001g0159 others(32): Show |
35 | HG00423.hp2 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2043+190_2043+192d others(5): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAA | 10 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0206 others(7): Show |
10 | HG01071.hp2 HG02293.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2043+189_2043+192d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0128 others(6): Show |
10 | HG02922.hp2 HG02965.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2043+187_2043+192d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0086 others(5): Show |
8 | HG01952.hp2 HG02135.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.2043+184_2043+192d others(11): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(3): Show |
26 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0034 others(23): Show |
26 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2043+183_2043+192d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(4): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(22): Show |
27 | HG00558.hp2 HG01928.hp2 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.2043+182_2043+192d others(13): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0042 others(12): Show |
15 | HG00408.hp2 HG01192.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2043+181_2043+192d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(4): Show |
7 | HG00423.hp1 HG02080.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+180_2043+192d others(15): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0082 others(4): Show |
7 | HG00673.hp2 NA18954.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+179_2043+192d others(16): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2043+178_2043+192d others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2043+176_2043+192d others(19): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2043+172_2043+192d others(23): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2043+171_2043+192d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0095 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2043+170_2043+192d others(25): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688114 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2043+181_2043+192d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | |||||||
| chr21:31688700 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(110): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1886-236G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688700 | |||||||
| chr21:31688714 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1886-250A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688714 | |||||||
| chr21:31688738 | C | T | 3 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0011t0001g0321 |
4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1886-274G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688738 | |||||||
| chr21:31688966 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1886-502A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688966 | |||||||
| chr21:31689015 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1886-551C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689015 | |||||||
| chr21:31689417 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1886-953G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689417 | |||||||
| chr21:31689464 | A | AT | 9 | a0001c0001t0001g0259 a0001c0001t0001g0301 a0001c0001t0001g0309 others(6): Show |
9 | HG01192.hp1 HG01934.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1886-1001dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | |||||||
| chr21:31689464 | AT | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(84): Show |
90 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1886-1001delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | |||||||
| chr21:31689464 | ATT | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(22): Show |
26 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1886-1002_1886-100 others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | |||||||
| chr21:31689614 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886-1150T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689614 | |||||||
| chr21:31689683 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(112): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1885+1114T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689683 | |||||||
| chr21:31689755 | C | A | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1885+1042G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689755 | |||||||
| chr21:31689787 | T | C | 10 | a0001c0003t0001g0024 a0001c0003t0001g0119 a0001c0003t0001g0120 others(7): Show |
10 | HG01891.hp1 HG01952.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1885+1010A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689787 | |||||||
| chr21:31689792 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(10): Show |
15 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1885+1005A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689792 | |||||||
| chr21:31690038 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
127 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1885+759A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690038 | |||||||
| chr21:31690119 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0112 others(83): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1885+678G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690119 | |||||||
| chr21:31690355 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1885+442G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690355 | |||||||
| chr21:31690500 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1885+297T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690500 | |||||||
| chr21:31690519 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1885+278G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690519 | |||||||
| chr21:31690613 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1885+184C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690613 | |||||||
| chr21:31690636 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1885+161A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690636 | |||||||
| chr21:31690690 | A | C | 1 | a0001c0002t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1885+107T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690690 | |||||||
| chr21:31691041 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(96): Show |
101 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1729-88G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691041 | |||||||
| chr21:31691052 | C | G | 5 | a0001c0003t0001g0024 a0001c0003t0002g0002 a0001c0003t0002g0019 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1729-99G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691052 | |||||||
| chr21:31691383 | A | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1729-430T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691383 | |||||||
| chr21:31691394 | A | G | 2 | a0001c0002t0001g0148 a0001c0002t0002g0138 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1728+423T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691394 | |||||||
| chr21:31691672 | T | TA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(114): Show |
120 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1728+144dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691672 | |||||||
| chr21:31691672 | TA | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0130 others(18): Show |
22 | HG00738.hp1 HG01070.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1728+144delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691672 | |||||||
| chr21:31691781 | TA | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(8): Show |
13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1728+35delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691781 | |||||||
| chr21:31691782 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1728+35T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691782 | |||||||
| chr21:31692138 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1615-208T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 13/19 | chr21 | 31692138 | |||||||
| chr21:31692232 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1614+117A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 13/19 | chr21 | 31692232 | |||||||
| chr21:31692705 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1514-256A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31692705 | |||||||
| chr21:31692803 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0225 |
4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1514-354G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31692803 | |||||||
| chr21:31693116 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1513+178C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31693116 | |||||||
| chr21:31693285 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513+9A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31693285 | |||||||
| chr21:31693566 | C | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02109.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1323-82G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693566 | |||||||
| chr21:31693617 | A | T | 1 | a0001c0003t0002g0002 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1323-133T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693617 | |||||||
| chr21:31693821 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0118 others(82): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1323-337G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693821 | |||||||
| chr21:31694108 | C | T | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322+96G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694108 | |||||||
| chr21:31694110 | A | G | 4 | a0001c0001t0001g0175 a0001c0005t0001g0340 a0001c0005t0002g0339 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1322+94T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694110 | |||||||
| chr21:31694168 | T | C | 13 | a0001c0003t0001g0024 a0001c0003t0001g0119 a0001c0003t0001g0120 others(10): Show |
14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1322+36A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694168 | |||||||
| chr21:31694390 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1237-101C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694390 | |||||||
| chr21:31694391 | C | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0292 |
2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1237-102G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694391 | |||||||
| chr21:31694441 | C | G | 2 | a0001c0005t0001g0340 a0001c0005t0002g0339 |
2 | HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1237-152G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694441 | |||||||
| chr21:31694463 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1237-174G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694463 | |||||||
| chr21:31694483 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1237-194A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694483 | |||||||
| chr21:31694607 | A | G | 1 | a0001c0002t0006g0342 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1236+206T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694607 | |||||||
| chr21:31694620 | C | T | 1 | a0007c0010t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1236+193G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694620 | |||||||
| chr21:31695114 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1069-134G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695114 | |||||||
| chr21:31695138 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1069-158G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695138 | |||||||
| chr21:31695398 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(105): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1069-418G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695398 | |||||||
| chr21:31695455 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1069-475T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695455 | |||||||
| chr21:31695495 | A | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0096 |
3 | NA18973.hp2 NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1069-515T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695495 | |||||||
| chr21:31695618 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG02257.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+495G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695618 | |||||||
| chr21:31695999 | A | G | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1068+114T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695999 | |||||||
| chr21:31696026 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1068+87G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31696026 | |||||||
| chr21:31696329 | A | G | 1 | a0001c0003t0002g0002 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.960-108T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696329 | |||||||
| chr21:31696338 | T | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0211 |
2 | NA18974.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.960-117A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696338 | |||||||
| chr21:31696393 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.960-172G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696393 | |||||||
| chr21:31696508 | G | C | 2 | a0001c0001t0001g0259 a0001c0001t0004g0275 |
2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.959+61C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696508 | |||||||
| chr21:31696813 | T | C | 20 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0150 others(17): Show |
20 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-63A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31696813 | |||||||
| chr21:31696894 | C | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0298 a0001c0001t0001g0302 others(2): Show |
5 | HG00544.hp1 NA18949.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-144G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31696894 | |||||||
| chr21:31697042 | T | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0227 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.778-292A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697042 | |||||||
| chr21:31697108 | T | C | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(1): Show |
4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-358A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697108 | |||||||
| chr21:31697315 | C | T | 19 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0150 others(16): Show |
19 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.778-565G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697315 | |||||||
| chr21:31697523 | T | C | 1 | a0001c0003t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.778-773A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697523 | |||||||
| chr21:31697608 | A | C | 1 | a0001c0002t0001g0209 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.778-858T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697608 | |||||||
| chr21:31697939 | T | A | 12 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(9): Show |
13 | HG01106.hp1 HG01952.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.778-1189A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697939 | |||||||
| chr21:31697974 | C | T | 8 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(5): Show |
8 | NA18942.hp2 NA18945.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-1224G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697974 | |||||||
| chr21:31698024 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-1274G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698024 | |||||||
| chr21:31698069 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.778-1319C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698069 | |||||||
| chr21:31698085 | A | C | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.778-1335T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698085 | |||||||
| chr21:31698091 | G | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.778-1341C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698091 | |||||||
| chr21:31698183 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.778-1433C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698183 | |||||||
| chr21:31698205 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.778-1455C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698205 | |||||||
| chr21:31698272 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0093 |
2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.778-1522A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698272 | |||||||
| chr21:31698346 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0069 others(1): Show |
4 | HG01192.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1596C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698346 | |||||||
| chr21:31698568 | T | C | 13 | a0001c0003t0001g0024 a0001c0003t0001g0119 a0001c0003t0001g0120 others(10): Show |
14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-1818A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698568 | |||||||
| chr21:31698703 | A | G | 13 | a0001c0003t0001g0024 a0001c0003t0001g0119 a0001c0003t0001g0120 others(10): Show |
14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-1953T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698703 | |||||||
| chr21:31698843 | C | A | 1 | a0001c0001t0001g0027 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.778-2093G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698843 | |||||||
| chr21:31698851 | A | C | 13 | a0001c0003t0001g0024 a0001c0003t0001g0119 a0001c0003t0001g0120 others(10): Show |
14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-2101T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698851 | |||||||
| chr21:31698983 | AC | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+2011delG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698983 | |||||||
| chr21:31699028 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+1967C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699028 | |||||||
| chr21:31699410 | A | G | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.777+1585T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699410 | |||||||
| chr21:31699501 | TG | T | 5 | a0001c0004t0001g0186 a0001c0004t0001g0187 a0001c0004t0001g0188 others(2): Show |
5 | HG00639.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1493delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699501 | |||||||
| chr21:31699502 | G | T | 1 | a0001c0004t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.777+1493C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | |||||||
| chr21:31699502 | GT | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0045 others(23): Show |
27 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.777+1492delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | |||||||
| chr21:31699502 | GTT | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(17): Show |
22 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.777+1491_777+1492d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | |||||||
| chr21:31699586 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+1409T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699586 | |||||||
| chr21:31699621 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0326 |
3 | HG01346.hp2 HG01943.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.777+1374C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699621 | |||||||
| chr21:31699717 | A | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.777+1278T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699717 | |||||||
| chr21:31699864 | T | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0299 a0001c0001t0001g0301 |
3 | HG00642.hp2 HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.777+1131A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699864 | |||||||
| chr21:31699887 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.777+1108C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699887 | |||||||
| chr21:31699975 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 |
3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.777+1020G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699975 | |||||||
| chr21:31699988 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+1007C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699988 | |||||||
| chr21:31700050 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(95): Show |
100 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+945A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700050 | |||||||
| chr21:31700123 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.777+872C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700123 | |||||||
| chr21:31700158 | AC | A | 9 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0191 others(6): Show |
9 | HG01071.hp2 HG01928.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.777+836delG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700158 | |||||||
| chr21:31700182 | T | TCA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0091 others(124): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+811_777+812dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700182 | |||||||
| chr21:31700234 | AAAT | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+758_777+760del others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700234 | |||||||
| chr21:31700290 | C | G | 2 | a0001c0003t0001g0119 a0001c0003t0001g0120 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.777+705G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700290 | |||||||
| chr21:31700351 | C | T | 1 | a0001c0004t0001g0014 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.777+644G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700351 | |||||||
| chr21:31700352 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.777+643C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700352 | |||||||
| chr21:31700410 | G | C | 2 | a0001c0003t0001g0126 a0001c0003t0002g0127 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.777+585C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700410 | |||||||
| chr21:31700544 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.777+451T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700544 | |||||||
| chr21:31700570 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+425A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700570 | |||||||
| chr21:31700574 | A | G | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.777+421T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700574 | |||||||
| chr21:31700741 | C | CT | 19 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0128 others(16): Show |
21 | HG01106.hp1 HG01109.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.777+253dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700741 | |||||||
| chr21:31700741 | C | CTT | 8 | a0001c0002t0001g0183 a0001c0003t0001g0119 a0001c0003t0001g0120 others(5): Show |
8 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+252_777+253dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700741 | |||||||
| chr21:31700812 | A | T | 3 | a0002c0006t0001g0271 a0002c0006t0001g0304 a0002c0006t0001g0322 |
3 | HG01074.hp2 HG01243.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.777+183T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700812 | |||||||
| chr21:31701350 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.601-179A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701350 | |||||||
| chr21:31701479 | G | A | 1 | a0002c0006t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.600+297C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701479 | |||||||
| chr21:31701608 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.600+168G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701608 | |||||||
| chr21:31701630 | A | C | 10 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(7): Show |
10 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.600+146T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701630 | |||||||
| chr21:31701698 | T | C | 5 | a0001c0004t0001g0186 a0001c0004t0001g0187 a0001c0004t0001g0188 others(2): Show |
5 | HG02723.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+78A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701698 | |||||||
| chr21:31701737 | A | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.600+39T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701737 | |||||||
| chr21:31702034 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458-116C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/19 | chr21 | 31702034 | |||||||
| chr21:31702382 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.322-3C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702382 | |||||||
| chr21:31702528 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG00099.hp1 HG01978.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.322-149T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702528 | |||||||
| chr21:31702611 | A | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.322-232T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702611 | |||||||
| chr21:31702733 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-354T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702733 | |||||||
| chr21:31702904 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-525T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702904 | |||||||
| chr21:31702968 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.322-589A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702968 | |||||||
| chr21:31703091 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(114): Show |
120 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.321+674A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703091 | |||||||
| chr21:31703114 | A | C | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+651T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703114 | |||||||
| chr21:31703192 | C | CA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(114): Show |
120 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.321+572dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703192 | |||||||
| chr21:31703239 | A | C | 2 | a0001c0003t0001g0126 a0001c0003t0002g0127 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.321+526T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703239 | |||||||
| chr21:31703290 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+475G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703290 | |||||||
| chr21:31703330 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
243 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.321+435T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703330 | |||||||
| chr21:31703356 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.321+409A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703356 | |||||||
| chr21:31703629 | A | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(9): Show |
13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+136T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703629 | |||||||
| chr21:31704261 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0326 |
3 | HG01346.hp2 HG01943.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.160-335G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704261 | |||||||
| chr21:31704336 | C | G | 1 | a0001c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160-410G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704336 | |||||||
| chr21:31704532 | C | CA | 13 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0273 others(10): Show |
13 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.160-607dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704532 | |||||||
| chr21:31704532 | C | CAA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-608_160-607dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704532 | |||||||
| chr21:31704558 | A | C | 1 | a0001c0013t0001g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.160-632T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704558 | |||||||
| chr21:31704594 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-668G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704594 | |||||||
| chr21:31704620 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.160-694T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704620 | |||||||
| chr21:31704621 | C | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(322): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.160-695G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704621 | |||||||
| chr21:31704636 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160-710C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704636 | |||||||
| chr21:31704651 | A | T | 1 | a0001c0002t0001g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.160-725T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704651 | |||||||
| chr21:31704710 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(9): Show |
13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+713T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704710 | |||||||
| chr21:31705500 | TTTAC | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0225 |
4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-37_115-34delGT others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705500 | |||||||
| chr21:31705526 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.115-59A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705526 | |||||||
| chr21:31705551 | T | C | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115-84A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705551 | |||||||
| chr21:31705957 | C | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.114+317G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705957 | |||||||
| chr21:31706037 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.114+237A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706037 | |||||||
| chr21:31706052 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(19): Show |
23 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+222C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706052 | |||||||
| chr21:31706168 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA19057.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.114+106A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706168 | |||||||
| chr21:31706175 | G | A | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.114+99C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706175 | |||||||
| chr21:31706414 | G | C | 7 | a0001c0001t0001g0079 a0001c0001t0001g0106 a0001c0001t0001g0314 others(4): Show |
8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-57C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706414 | |||||||
| chr21:31706424 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-67A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706424 | |||||||
| chr21:31706473 | AG | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-117delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706473 | |||||||
| chr21:31706513 | T | C | 23 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0105 others(20): Show |
23 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-156A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706513 | |||||||
| chr21:31706600 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.31-243C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706600 | |||||||
| chr21:31706612 | G | A | 106 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(103): Show |
109 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-255C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706612 | |||||||
| chr21:31706629 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-272C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706629 | |||||||
| chr21:31706660 | A | G | 4 | a0001c0001t0001g0221 a0001c0003t0002g0002 a0001c0003t0002g0019 others(1): Show |
5 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-303T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706660 | |||||||
| chr21:31706803 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.31-446G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706803 | |||||||
| chr21:31706816 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 |
3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.31-459T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706816 | |||||||
| chr21:31706827 | T | TC | 6 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0122 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-471dupG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706827 | |||||||
| chr21:31706842 | A | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0173 |
3 | HG02486.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.31-485T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706842 | |||||||
| chr21:31706893 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-536C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706893 | |||||||
| chr21:31707001 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31-644T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707001 | |||||||
| chr21:31707153 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-796A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707153 | |||||||
| chr21:31707312 | C | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-955G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707312 | |||||||
| chr21:31707445 | A | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1088T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707445 | |||||||
| chr21:31707480 | T | TAAGG | 9 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-1124_31-1123ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707480 | |||||||
| chr21:31707488 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-1131T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707488 | |||||||
| chr21:31707526 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1169G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707526 | |||||||
| chr21:31707717 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.31-1360A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707717 | |||||||
| chr21:31707770 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1413G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707770 | |||||||
| chr21:31708000 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0021 others(61): Show |
65 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.31-1643C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708000 | |||||||
| chr21:31708125 | T | C | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-1768A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708125 | |||||||
| chr21:31708196 | T | C | 2 | a0001c0001t0003g0169 a0001c0001t0003g0215 |
2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.31-1839A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708196 | |||||||
| chr21:31708277 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-1920C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708277 | |||||||
| chr21:31708290 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1933G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708290 | |||||||
| chr21:31708290 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-1933G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708290 | |||||||
| chr21:31708308 | G | A | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-1951C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708308 | |||||||
| chr21:31708437 | T | C | 6 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(3): Show |
7 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-2080A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708437 | |||||||
| chr21:31708526 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-2169A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708526 | |||||||
| chr21:31708665 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-2308G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708665 | |||||||
| chr21:31708678 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-2321G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708678 | |||||||
| chr21:31708860 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.31-2503T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708860 | |||||||
| chr21:31708891 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.31-2534C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708891 | |||||||
| chr21:31709144 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0004g0275 |
2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.31-2787A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709144 | |||||||
| chr21:31709202 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-2845C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709202 | |||||||
| chr21:31709268 | C | T | 1 | a0001c0002t0001g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.31-2911G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709268 | |||||||
| chr21:31709350 | C | CA | 18 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0170 others(15): Show |
19 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-2994dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | |||||||
| chr21:31709350 | C | CAA | 12 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-2995_31-2994dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | |||||||
| chr21:31709350 | C | CAAA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(82): Show |
87 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-2996_31-2994dup others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | |||||||
| chr21:31709361 | A | G | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-3004T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709361 | |||||||
| chr21:31709692 | C | A | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.31-3335G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709692 | |||||||
| chr21:31709774 | G | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0293 |
2 | NA18998.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.31-3417C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709774 | |||||||
| chr21:31709844 | AGAT | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(103): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-3490_31-3488del others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709844 | |||||||
| chr21:31709854 | TA | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(31): Show |
36 | HG00738.hp1 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-3498delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709854 | |||||||
| chr21:31709874 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-3517G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709874 | |||||||
| chr21:31710029 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
99 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.31-3672A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710029 | |||||||
| chr21:31710069 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.31-3712G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710069 | |||||||
| chr21:31710156 | T | C | 4 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0001g0332 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3799A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710156 | |||||||
| chr21:31710181 | C | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-3824G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710181 | |||||||
| chr21:31710219 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-3862C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710219 | |||||||
| chr21:31710319 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.31-3962G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710319 | |||||||
| chr21:31710481 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.31-4124C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710481 | |||||||
| chr21:31710749 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.31-4392C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710749 | |||||||
| chr21:31711205 | C | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0292 |
2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.31-4848G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711205 | |||||||
| chr21:31711461 | T | C | 1 | a0001c0002t0001g0176 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-5104A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711461 | |||||||
| chr21:31711515 | T | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5158A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711515 | |||||||
| chr21:31711729 | A | C | 2 | a0001c0001t0001g0217 a0001c0001t0004g0218 |
2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.31-5372T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711729 | |||||||
| chr21:31711944 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0236 others(81): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.31-5587T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711944 | |||||||
| chr21:31711987 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31-5630A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711987 | |||||||
| chr21:31712039 | T | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5682A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712039 | |||||||
| chr21:31712047 | T | G | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31-5690A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712047 | |||||||
| chr21:31712222 | C | CT | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.31-5866dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | |||||||
| chr21:31712222 | C | CTT | 6 | a0001c0001t0001g0173 a0001c0001t0001g0278 a0001c0001t0001g0298 others(3): Show |
6 | HG03239.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-5867_31-5866dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | |||||||
| chr21:31712222 | C | CTTTTTTT others(5): Show |
1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5877_31-5866dup others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | |||||||
| chr21:31712308 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0118 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.31-5951G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712308 | |||||||
| chr21:31712362 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-6005G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712362 | |||||||
| chr21:31712373 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6016T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712373 | |||||||
| chr21:31712410 | G | T | 1 | a0004c0016t0001g0297 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.31-6053C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712410 | |||||||
| chr21:31712527 | C | CT | 23 | a0001c0001t0001g0092 a0001c0001t0001g0132 a0001c0001t0001g0137 others(20): Show |
23 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-6171dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | |||||||
| chr21:31712527 | C | CTT | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-6172_31-6171dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | |||||||
| chr21:31712527 | CT | C | 6 | a0001c0001t0001g0085 a0001c0001t0002g0056 a0001c0003t0001g0126 others(3): Show |
7 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-6171delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | |||||||
| chr21:31712527 | CTT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6172_31-6171del others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | |||||||
| chr21:31712789 | C | CAA | 3 | a0001c0001t0002g0262 a0001c0007t0001g0296 a0001c0007t0001g0319 |
3 | NA18954.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31-6434_31-6433dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712789 | |||||||
| chr21:31712809 | C | T | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-6452G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712809 | |||||||
| chr21:31712898 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.31-6541T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712898 | |||||||
| chr21:31712904 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6547A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712904 | |||||||
| chr21:31713019 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.31-6662T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713019 | |||||||
| chr21:31713112 | TTACTTGT others(10): Show |
T | 1 | a0001c0002t0002g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.31-6772_31-6756del others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713112 | |||||||
| chr21:31713272 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0118 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.31-6915C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713272 | |||||||
| chr21:31713380 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0260 a0001c0001t0001g0295 others(1): Show |
4 | HG02135.hp2 NA19000.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7023A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713380 | |||||||
| chr21:31713484 | C | T | 19 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0150 others(16): Show |
19 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-7127G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713484 | |||||||
| chr21:31713505 | A | G | 2 | a0001c0001t0001g0107 a0001c0011t0001g0321 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-7148T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713505 | |||||||
| chr21:31713541 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-7184T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713541 | |||||||
| chr21:31713741 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0293 |
2 | NA18998.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.31-7384C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713741 | |||||||
| chr21:31713745 | C | T | 5 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0005t0001g0340 others(2): Show |
5 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7388G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713745 | |||||||
| chr21:31713746 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-7389C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713746 | |||||||
| chr21:31713756 | T | TG | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(137): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.31-7400dupC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713756 | |||||||
| chr21:31713763 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-7406C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713763 | |||||||
| chr21:31713815 | A | G | 3 | a0001c0001t0001g0172 a0001c0004t0001g0012 a0001c0004t0001g0013 |
3 | HG01891.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.31-7458T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713815 | |||||||
| chr21:31713819 | T | G | 1 | a0001c0003t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31-7462A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713819 | |||||||
| chr21:31713864 | G | C | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-7507C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713864 | |||||||
| chr21:31713960 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.31-7603A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713960 | |||||||
| chr21:31714026 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.31-7669C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714026 | |||||||
| chr21:31714078 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.31-7721T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714078 | |||||||
| chr21:31714184 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-7827T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714184 | |||||||
| chr21:31714344 | T | C | 25 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(22): Show |
25 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-7987A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714344 | |||||||
| chr21:31714478 | G | A | 1 | a0001c0003t0001g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.31-8121C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714478 | |||||||
| chr21:31714493 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31-8136G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714493 | |||||||
| chr21:31714526 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-8169G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714526 | |||||||
| chr21:31714554 | T | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-8197A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714554 | |||||||
| chr21:31714995 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-8638A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714995 | |||||||
| chr21:31715044 | G | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(23): Show |
27 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-8687C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715044 | |||||||
| chr21:31715108 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0118 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.31-8751A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715108 | |||||||
| chr21:31715250 | C | A | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-8893G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715250 | |||||||
| chr21:31715550 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-9193T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715550 | |||||||
| chr21:31715642 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-9285G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715642 | |||||||
| chr21:31715703 | G | A | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-9346C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715703 | |||||||
| chr21:31715928 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-9571C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715928 | |||||||
| chr21:31716048 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.31-9691C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716048 | |||||||
| chr21:31716164 | CT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-9808delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716164 | |||||||
| chr21:31716280 | G | C | 1 | a0001c0001t0002g0320 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.31-9923C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716280 | |||||||
| chr21:31716580 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.31-10223G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716580 | |||||||
| chr21:31716582 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.31-10225G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716582 | |||||||
| chr21:31716697 | AG | A | 3 | a0001c0001t0002g0262 a0001c0007t0001g0296 a0001c0007t0001g0319 |
3 | NA18954.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31-10341delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716697 | |||||||
| chr21:31716808 | A | G | 2 | a0001c0003t0001g0119 a0001c0003t0001g0120 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-10451T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716808 | |||||||
| chr21:31717033 | T | C | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-10676A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717033 | |||||||
| chr21:31717095 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-10738G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717095 | |||||||
| chr21:31717149 | G | A | 2 | a0001c0003t0001g0119 a0001c0003t0001g0120 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-10792C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717149 | |||||||
| chr21:31717390 | A | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11033T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717390 | |||||||
| chr21:31717795 | A | C | 1 | a0001c0001t0001g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.31-11438T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717795 | |||||||
| chr21:31717806 | A | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11449T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717806 | |||||||
| chr21:31717807 | A | T | 3 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0011t0001g0321 |
3 | HG00639.hp1 HG02970.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.31-11450T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717807 | |||||||
| chr21:31717826 | C | CAT | 20 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0044 others(17): Show |
20 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-11471_31-11470d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | |||||||
| chr21:31717826 | C | CATATAT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0021 others(36): Show |
40 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-11475_31-11470d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | |||||||
| chr21:31717826 | C | CATATATA others(1): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0108 others(3): Show |
6 | HG00544.hp2 HG02074.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11477_31-11470d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | |||||||
| chr21:31717826 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.31-11481_31-11470d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | |||||||
| chr21:31717826 | CATAT | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11473_31-11470d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | |||||||
| chr21:31717840 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-11483A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717840 | |||||||
| chr21:31717840 | T | TAC | 7 | a0001c0001t0001g0177 a0001c0001t0001g0247 a0001c0001t0001g0264 others(4): Show |
7 | HG02040.hp2 HG02602.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11484_31-11483i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717840 | |||||||
| chr21:31717842 | T | C | 14 | a0001c0001t0001g0118 a0001c0001t0001g0135 a0001c0001t0001g0177 others(11): Show |
14 | HG00544.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-11485A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TAC | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0133 others(102): Show |
108 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.31-11487_31-11486d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TACAC | 23 | a0001c0001t0001g0006 a0001c0001t0001g0132 a0001c0001t0001g0134 others(20): Show |
24 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-11489_31-11486d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TACACAC | 6 | a0001c0001t0001g0137 a0001c0001t0001g0191 a0001c0001t0001g0197 others(3): Show |
6 | HG01071.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11491_31-11486d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TATAC | 22 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0193 others(19): Show |
22 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-11486_31-11485i others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TATATAC | 4 | a0001c0001t0001g0071 a0001c0001t0001g0084 a0001c0001t0001g0086 others(1): Show |
4 | HG02273.hp2 NA18963.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11486_31-11485i others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TATATATA others(1): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG01167.hp2 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.31-11486_31-11485i others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.31-11486_31-11485i others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717842 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31-11486_31-11485i others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | |||||||
| chr21:31717844 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(80): Show |
87 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-11487G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717844 | |||||||
| chr21:31717846 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(62): Show |
67 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.31-11489G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717846 | |||||||
| chr21:31717848 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(54): Show |
59 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.31-11491G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717848 | |||||||
| chr21:31717850 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(32): Show |
36 | HG00621.hp1 HG00639.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-11493G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717850 | |||||||
| chr21:31717852 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
27 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-11495G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717852 | |||||||
| chr21:31717854 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0085 a0001c0001t0001g0088 |
3 | HG03834.hp2 HG04115.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.31-11497G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717854 | |||||||
| chr21:31717856 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-11499G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717856 | |||||||
| chr21:31717860 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11503G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717860 | |||||||
| chr21:31717862 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11505G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717862 | |||||||
| chr21:31717864 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11507G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717864 | |||||||
| chr21:31717864 | CACACACA others(3): Show |
C | 2 | a0001c0003t0001g0119 a0001c0003t0001g0120 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-11517_31-11508d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717864 | |||||||
| chr21:31717866 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
8 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-11509G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717866 | |||||||
| chr21:31717866 | CACACATA others(1): Show |
C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0107 others(6): Show |
9 | HG01243.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-11517_31-11510d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717866 | |||||||
| chr21:31717868 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(63): Show |
68 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.31-11511G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717868 | |||||||
| chr21:31717870 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(67): Show |
72 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.31-11513G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | |||||||
| chr21:31717870 | CAT | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0106 others(2): Show |
6 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11515_31-11514d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | |||||||
| chr21:31717870 | CATAT | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-11517_31-11514d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | |||||||
| chr21:31717872 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(50): Show |
55 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.31-11515A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717872 | |||||||
| chr21:31717874 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
63 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.31-11517A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717874 | |||||||
| chr21:31717876 | C | T | 2 | a0001c0003t0001g0122 a0001c0003t0001g0123 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11519G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717876 | |||||||
| chr21:31717878 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(48): Show |
53 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.31-11521G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717878 | |||||||
| chr21:31717880 | T | C | 10 | a0001c0001t0001g0168 a0001c0001t0001g0199 a0001c0002t0001g0147 others(7): Show |
10 | HG02015.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-11523A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717880 | |||||||
| chr21:31717880 | TATATACA others(1): Show |
T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11531_31-11524d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717880 | |||||||
| chr21:31717886 | C | T | 2 | a0001c0003t0001g0122 a0001c0003t0001g0123 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11529G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717886 | |||||||
| chr21:31717888 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-11531G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717888 | |||||||
| chr21:31717890 | T | C | 2 | a0001c0003t0001g0122 a0001c0003t0001g0123 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11533A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717890 | |||||||
| chr21:31717890 | TATATACA others(19): Show |
T | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-11559_31-11534d others(28): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717890 | |||||||
| chr21:31717892 | T | C | 1 | a0001c0003t0001g0125 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31-11535A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717892 | |||||||
| chr21:31717892 | TATACACA others(15): Show |
T | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-11557_31-11536d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717892 | |||||||
| chr21:31717894 | T | C | 4 | a0001c0003t0001g0122 a0001c0003t0001g0123 a0001c0003t0001g0124 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11537A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717894 | |||||||
| chr21:31717896 | CACATATA others(1): Show |
C | 4 | a0001c0002t0001g0148 a0001c0002t0001g0202 a0001c0002t0002g0138 others(1): Show |
4 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11547_31-11540d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717896 | |||||||
| chr21:31717898 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11541G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | |||||||
| chr21:31717898 | CAT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0061 others(12): Show |
15 | HG00621.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-11543_31-11542d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | |||||||
| chr21:31717898 | CATATAT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0002t0001g0147 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11547_31-11542d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | |||||||
| chr21:31717900 | T | C | 4 | a0001c0002t0001g0146 a0001c0003t0001g0121 a0001c0003t0001g0124 others(1): Show |
4 | HG00741.hp2 HG01952.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11543A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717900 | |||||||
| chr21:31717900 | TATATACA others(5): Show |
T | 1 | a0001c0003t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-11555_31-11544d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717900 | |||||||
| chr21:31717902 | T | C | 6 | a0001c0002t0001g0146 a0001c0003t0001g0119 a0001c0003t0001g0120 others(3): Show |
6 | HG00741.hp2 HG01952.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11545A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | |||||||
| chr21:31717902 | T | TAC | 4 | a0001c0001t0002g0104 a0001c0002t0006g0342 a0001c0003t0001g0024 others(1): Show |
4 | HG01891.hp1 HG01934.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11546_31-11545i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | |||||||
| chr21:31717902 | T | TACAC | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0105 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11546_31-11545i others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | |||||||
| chr21:31717902 | TATAC | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(21): Show |
24 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-11549_31-11546d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | |||||||
| chr21:31717902 | TATACAC | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0092 others(8): Show |
11 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-11551_31-11546d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | |||||||
| chr21:31717904 | T | C | 26 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0073 others(23): Show |
26 | HG00741.hp2 HG01891.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-11547A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | T | TAC | 18 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0175 others(15): Show |
18 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-11549_31-11548d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | T | TACAC | 9 | a0001c0001t0001g0221 a0001c0001t0001g0246 a0001c0001t0001g0274 others(6): Show |
9 | HG00741.hp1 HG01074.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-11551_31-11548d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | T | TACACAC | 11 | a0001c0001t0001g0001 a0001c0001t0001g0269 a0001c0001t0001g0292 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-11553_31-11548d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0225 a0001c0001t0001g0245 a0001c0002t0001g0209 others(1): Show |
4 | HG00639.hp2 HG01168.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11557_31-11548d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TAC | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0043 others(64): Show |
68 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.31-11549_31-11548d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACAC | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0040 others(39): Show |
42 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.31-11551_31-11548d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACACAC | T | 13 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0160 others(10): Show |
13 | HG01358.hp2 HG01934.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-11553_31-11548d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0237 others(1): Show |
4 | HG00140.hp1 HG03831.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11555_31-11548d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11557_31-11548d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0315 a0001c0001t0003g0011 a0001c0001t0003g0329 |
3 | HG02818.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.31-11559_31-11548d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717904 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.31-11561_31-11548d others(16): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | |||||||
| chr21:31717906 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11549G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717906 | |||||||
| chr21:31717908 | C | CAT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0026 others(25): Show |
29 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11552_31-11551i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717908 | |||||||
| chr21:31717910 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(35): Show |
41 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-11553G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717910 | |||||||
| chr21:31717912 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0028 others(30): Show |
36 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-11555G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717912 | |||||||
| chr21:31717914 | C | T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0040 others(25): Show |
29 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11557G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717914 | |||||||
| chr21:31717916 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(18): Show |
22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-11559G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717916 | |||||||
| chr21:31717918 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.31-11561G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717918 | |||||||
| chr21:31717920 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11563G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717920 | |||||||
| chr21:31717922 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11565G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717922 | |||||||
| chr21:31717938 | CACACACA others(3): Show |
C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11591_31-11582d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717938 | |||||||
| chr21:31717940 | CACACACA others(1): Show |
C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0178 a0001c0002t0001g0144 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11591_31-11584d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717940 | |||||||
| chr21:31717946 | CAT | C | 7 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0001g0224 others(4): Show |
7 | HG01074.hp1 HG01099.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11591_31-11590d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717946 | |||||||
| chr21:31717948 | T | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0094 others(4): Show |
7 | HG02486.hp1 HG02818.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11591A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717948 | |||||||
| chr21:31718069 | A | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11712T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718069 | |||||||
| chr21:31718108 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11751A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718108 | |||||||
| chr21:31718366 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.31-12009A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718366 | |||||||
| chr21:31718445 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
99 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.31-12088C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718445 | |||||||
| chr21:31718472 | T | C | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-12115A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718472 | |||||||
| chr21:31718505 | A | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(91): Show |
96 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.31-12148T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718505 | |||||||
| chr21:31718575 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-12218G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718575 | |||||||
| chr21:31718651 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0002g0127 |
2 | HG03225.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.31-12294C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718651 | |||||||
| chr21:31718771 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-12414G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718771 | |||||||
| chr21:31718780 | T | C | 1 | a0001c0004t0001g0014 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31-12423A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718780 | |||||||
| chr21:31718976 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.31-12619A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718976 | |||||||
| chr21:31719120 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+12543T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719120 | |||||||
| chr21:31719161 | A | G | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+12502T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719161 | |||||||
| chr21:31719289 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+12374G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719289 | |||||||
| chr21:31719322 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+12341T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719322 | |||||||
| chr21:31719459 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30+12204A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719459 | |||||||
| chr21:31719498 | A | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0128 others(7): Show |
11 | HG02615.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+12165T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719498 | |||||||
| chr21:31719501 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0093 |
3 | HG02155.hp1 NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.30+12162G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719501 | |||||||
| chr21:31719608 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0003g0169 a0001c0001t0003g0215 |
3 | HG00642.hp1 HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.30+12055C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719608 | |||||||
| chr21:31719710 | G | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+11953C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719710 | |||||||
| chr21:31719774 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+11889C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719774 | |||||||
| chr21:31719953 | T | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+11710A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719953 | |||||||
| chr21:31720200 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+11463A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720200 | |||||||
| chr21:31720455 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30+11208G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720455 | |||||||
| chr21:31720468 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0005g0020 others(1): Show |
4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+11195C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720468 | |||||||
| chr21:31720468 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0117 |
2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.30+11195C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720468 | |||||||
| chr21:31720530 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0170 a0001c0001t0001g0171 others(12): Show |
16 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+11133C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720530 | |||||||
| chr21:31720737 | T | C | 8 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(5): Show |
8 | NA18942.hp2 NA18945.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+10926A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720737 | |||||||
| chr21:31720893 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.30+10770T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720893 | |||||||
| chr21:31721219 | T | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+10444A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721219 | |||||||
| chr21:31721303 | T | C | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+10360A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721303 | |||||||
| chr21:31721307 | GTGATTTA others(15): Show |
G | 1 | a0001c0001t0004g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.30+10334_30+10355d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721307 | |||||||
| chr21:31721725 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0027 others(91): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.30+9937dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721725 | |||||||
| chr21:31721726 | T | C | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.30+9937A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721726 | |||||||
| chr21:31721758 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+9905C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721758 | |||||||
| chr21:31721767 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.30+9896G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721767 | |||||||
| chr21:31722000 | G | T | 1 | a0001c0003t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30+9663C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722000 | |||||||
| chr21:31722417 | T | C | 6 | a0001c0004t0001g0186 a0001c0004t0001g0187 a0001c0004t0001g0188 others(3): Show |
6 | HG00639.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+9246A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722417 | |||||||
| chr21:31722519 | C | T | 1 | a0001c0002t0004g0140 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.30+9144G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722519 | |||||||
| chr21:31722745 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+8918T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722745 | |||||||
| chr21:31722774 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+8889C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722774 | |||||||
| chr21:31722810 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0107 |
3 | HG01243.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.30+8853C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722810 | |||||||
| chr21:31722884 | C | T | 1 | a0001c0003t0001g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.30+8779G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722884 | |||||||
| chr21:31723051 | A | G | 1 | a0001c0002t0001g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.30+8612T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723051 | |||||||
| chr21:31723106 | T | A | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+8557A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723106 | |||||||
| chr21:31723172 | T | C | 2 | a0001c0003t0002g0002 a0001c0003t0002g0019 |
3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.30+8491A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723172 | |||||||
| chr21:31723298 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+8365T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723298 | |||||||
| chr21:31723321 | G | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8342C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723321 | |||||||
| chr21:31723452 | C | CA | 21 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0150 others(18): Show |
21 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8210dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723452 | |||||||
| chr21:31723471 | CAAACAAA others(5): Show |
C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8180_30+8191del others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723471 | |||||||
| chr21:31723481 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.30+8182T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723481 | |||||||
| chr21:31723502 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.30+8161A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723502 | |||||||
| chr21:31723609 | G | GTT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
22 | HG00621.hp1 HG01243.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | |||||||
| chr21:31723609 | G | GTTGT | 51 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
52 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | |||||||
| chr21:31723609 | G | GTTGTGT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
10 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | |||||||
| chr21:31723609 | G | GTTGTGTG others(5): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | |||||||
| chr21:31723610 | A | ATG | 13 | a0001c0001t0001g0134 a0001c0001t0001g0150 a0001c0001t0001g0151 others(10): Show |
13 | HG00741.hp2 HG01070.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+8051_30+8052dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | |||||||
| chr21:31723610 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
91 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+8053T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | |||||||
| chr21:31723610 | A | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0087 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.30+8053T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | |||||||
| chr21:31723627 | T | C | 2 | a0001c0001t0001g0303 a0002c0006t0001g0304 |
2 | HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.30+8036A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | |||||||
| chr21:31723627 | T | TGC | 9 | a0001c0001t0001g0225 a0001c0001t0001g0299 a0001c0001t0001g0300 others(6): Show |
9 | HG00642.hp2 HG01168.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+8035_30+8036ins others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | |||||||
| chr21:31723627 | T | TGCGC | 8 | a0001c0001t0001g0241 a0001c0001t0001g0305 a0001c0001t0001g0306 others(5): Show |
8 | HG01261.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8035_30+8036ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | |||||||
| chr21:31723629 | T | C | 25 | a0001c0001t0001g0225 a0001c0001t0001g0241 a0001c0001t0001g0269 others(22): Show |
25 | HG00642.hp2 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+8034A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGC | 54 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0118 others(51): Show |
56 | HG00140.hp1 HG00642.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+8032_30+8033dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGCGC | 29 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0276 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+8030_30+8033dup others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGC | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(8): Show |
11 | HG01433.hp1 HG02040.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGCGC | 8 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0237 others(5): Show |
8 | HG01074.hp2 HG02040.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGTGC | 12 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG00408.hp2 HG00544.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | T | TGTGTGTG others(15): Show |
1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(22): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723629 | TGCGC | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
21 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8030_30+8033del others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | |||||||
| chr21:31723631 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0105 others(15): Show |
20 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+8032G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723631 | |||||||
| chr21:31723633 | C | T | 4 | a0001c0001t0001g0023 a0001c0005t0001g0340 a0001c0005t0002g0339 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+8030G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723633 | |||||||
| chr21:31723635 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
21 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8028G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723635 | |||||||
| chr21:31723638 | G | A | 4 | a0001c0001t0003g0323 a0001c0001t0003g0327 a0001c0001t0003g0328 others(1): Show |
4 | HG03017.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+8025C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723638 | |||||||
| chr21:31723638 | G | T | 1 | a0001c0002t0002g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.30+8025C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723638 | |||||||
| chr21:31723646 | G | A | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+8017C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723646 | |||||||
| chr21:31723790 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+7873G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723790 | |||||||
| chr21:31723805 | G | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+7858C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723805 | |||||||
| chr21:31723821 | A | G | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+7842T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723821 | |||||||
| chr21:31723886 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+7777A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723886 | |||||||
| chr21:31724033 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.30+7630A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724033 | |||||||
| chr21:31724239 | A | ACACAGAA others(105): Show |
1 | a0001c0001t0001g0006 | 2 | NA18943.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.30+7423_30+7424ins others(112): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724239 | |||||||
| chr21:31724249 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+7414C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724249 | |||||||
| chr21:31724285 | G | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG00099.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.30+7378C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724285 | |||||||
| chr21:31724301 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.30+7362G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724301 | |||||||
| chr21:31724501 | T | G | 1 | a0001c0001t0001g0312 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.30+7162A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724501 | |||||||
| chr21:31724552 | G | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+7111C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724552 | |||||||
| chr21:31724554 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
125 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.30+7109A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724554 | |||||||
| chr21:31724580 | T | C | 1 | a0001c0002t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.30+7083A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724580 | |||||||
| chr21:31724665 | C | T | 1 | a0001c0001t0003g0323 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.30+6998G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724665 | |||||||
| chr21:31724740 | A | C | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG00423.hp2 HG02074.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.30+6923T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724740 | |||||||
| chr21:31724765 | T | A | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.30+6898A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724765 | |||||||
| chr21:31724896 | G | C | 1 | a0001c0001t0001g0313 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.30+6767C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724896 | |||||||
| chr21:31725198 | C | A | 4 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0001g0332 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+6465G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725198 | |||||||
| chr21:31725345 | T | C | 1 | a0001c0002t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+6318A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725345 | |||||||
| chr21:31725443 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+6220G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725443 | |||||||
| chr21:31725723 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+5940A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725723 | |||||||
| chr21:31725761 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
125 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.30+5902G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725761 | |||||||
| chr21:31725849 | C | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5814G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725849 | |||||||
| chr21:31725879 | C | T | 3 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG01175.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.30+5784G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725879 | |||||||
| chr21:31725884 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5779G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725884 | |||||||
| chr21:31725889 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5774G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725889 | |||||||
| chr21:31725891 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+5772A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725891 | |||||||
| chr21:31726098 | T | C | 1 | a0001c0002t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.30+5565A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726098 | |||||||
| chr21:31726191 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5472C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726191 | |||||||
| chr21:31726199 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+5464G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726199 | |||||||
| chr21:31726208 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.30+5455C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726208 | |||||||
| chr21:31726236 | G | A | 1 | a0001c0002t0006g0342 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+5427C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726236 | |||||||
| chr21:31726236 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5427C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726236 | |||||||
| chr21:31726302 | C | G | 1 | a0001c0001t0005g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+5361G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726302 | |||||||
| chr21:31726344 | G | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0314 a0001c0001t0001g0315 others(20): Show |
24 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.30+5319C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726344 | |||||||
| chr21:31726552 | C | T | 1 | a0001c0003t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+5111G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726552 | |||||||
| chr21:31726555 | C | T | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+5108G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726555 | |||||||
| chr21:31726565 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.30+5098A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726565 | |||||||
| chr21:31726596 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
7 | HG02615.hp2 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+5067G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726596 | |||||||
| chr21:31726724 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4939A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726724 | |||||||
| chr21:31726855 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
9 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+4808C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726855 | |||||||
| chr21:31726892 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.30+4771T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726892 | |||||||
| chr21:31727076 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.30+4587C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727076 | |||||||
| chr21:31727079 | CT | C | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+4583delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727079 | |||||||
| chr21:31727136 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+4527A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727136 | |||||||
| chr21:31727155 | T | G | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00099.hp2 HG01433.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4508A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727155 | |||||||
| chr21:31727415 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+4248A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727415 | |||||||
| chr21:31727535 | G | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+4128C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727535 | |||||||
| chr21:31727655 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.30+4008C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727655 | |||||||
| chr21:31727696 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+3967G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727696 | |||||||
| chr21:31727913 | A | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+3750T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727913 | |||||||
| chr21:31728194 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+3469C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728194 | |||||||
| chr21:31728482 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.30+3181G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728482 | |||||||
| chr21:31728487 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+3176T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728487 | |||||||
| chr21:31728561 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+3102G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728561 | |||||||
| chr21:31728657 | A | G | 7 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+3006T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728657 | |||||||
| chr21:31728658 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+3005A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728658 | |||||||
| chr21:31728844 | T | C | 1 | a0001c0007t0001g0319 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.30+2819A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728844 | |||||||
| chr21:31729020 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02109.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.30+2643G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729020 | |||||||
| chr21:31729267 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2396G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729267 | |||||||
| chr21:31729274 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+2389G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729274 | |||||||
| chr21:31729486 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.30+2177C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729486 | |||||||
| chr21:31729567 | G | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2096C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729567 | |||||||
| chr21:31729568 | G | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2095C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729568 | |||||||
| chr21:31729569 | G | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2094C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729569 | |||||||
| chr21:31729570 | G | C | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2093C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729570 | |||||||
| chr21:31729572 | A | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2091T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729572 | |||||||
| chr21:31729573 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2090G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729573 | |||||||
| chr21:31729574 | G | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2089C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729574 | |||||||
| chr21:31729579 | A | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2084T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729579 | |||||||
| chr21:31729580 | A | T | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2083T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729580 | |||||||
| chr21:31729686 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0236 others(103): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.30+1977A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729686 | |||||||
| chr21:31729691 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.30+1972T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729691 | |||||||
| chr21:31729695 | G | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+1968C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729695 | |||||||
| chr21:31729763 | T | C | 1 | a0001c0001t0002g0320 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.30+1900A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729763 | |||||||
| chr21:31729780 | T | C | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+1883A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729780 | |||||||
| chr21:31730415 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.30+1248G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730415 | |||||||
| chr21:31730423 | A | G | 9 | a0001c0003t0001g0119 a0001c0003t0001g0120 a0001c0003t0001g0121 others(6): Show |
9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+1240T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730423 | |||||||
| chr21:31730496 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+1167G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730496 | |||||||
| chr21:31730498 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(102): Show |
108 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.30+1165T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730498 | |||||||
| chr21:31730751 | T | C | 1 | a0002c0006t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+912A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730751 | |||||||
| chr21:31730845 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0324 a0001c0001t0001g0325 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+818C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730845 | |||||||
| chr21:31730866 | C | T | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.30+797G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730866 | |||||||
| chr21:31730927 | A | ACAACGCC others(6): Show |
1 | a0001c0002t0001g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.30+723_30+735dupAA others(11): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730927 | |||||||
| chr21:31731259 | C | T | 3 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG01175.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.30+404G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731259 | |||||||
| chr21:31731307 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+356C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731307 | |||||||
| chr21:31731336 | G | A | 3 | a0001c0005t0001g0340 a0001c0005t0002g0339 a0001c0005t0002g0341 |
3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+327C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731336 | |||||||
| chr21:31731381 | C | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.30+282G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731381 | |||||||
| chr21:31731638 | C | T | 1 | a0001c0001t0004g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+25G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731638 |